Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5783 |
|---|---|
| ensemblid | ENSG00000163629.13 |
| hgncid | 9646 |
| symbol | PTPN13 |
| name | protein tyrosine phosphatase non-receptor type 13 |
| refseq_nuc | NM_080683.3 |
| refseq_prot | NP_542414.1 |
| ensembl_nuc | ENST00000411767.7 |
| ensembl_prot | ENSP00000407249.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 86594315 |
| end | 86815161 |
| strand | + |
| ver | v1.2 |
| region | chr4:86594315-86815161 |
| region5000 | chr4:86589315-86820161 |
| regionname0 | PTPN13_chr4_86594315_86815161 |
| regionname5000 | PTPN13_chr4_86589315_86820161 |
| 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 | 1/0 | 2485 | 62 | 6 | 12 | 37 | 4 | 2 | 29 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0002 | 0/0 | 2485 | 53 | 0 | 12 | 34 | 5 | 2 | 27 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003 | 0/1 | 2485 | 43 | 28 | 7 | 7 | 0 | 0 | 6 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0004 | 0/0 | 2485 | 9 | 0 | 6 | 1 | 1 | 1 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0005 | 0/0 | 2485 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0006 | 0/0 | 2485 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0007 | 0/0 | 2485 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0008 | 0/0 | 2485 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0009 | 0/0 | 2485 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0010 | 0/0 | 2485 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0011 | 0/0 | 2485 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0012 | 0/0 | 2485 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0013 | 0/0 | 2485 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0014 | 0/0 | 2485 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0015 | 0/0 | 2485 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0016 | 0/0 | 2485 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0017 | 0/0 | 2485 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0018 | 0/0 | 2485 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0019 | 0/0 | 2485 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0020 | 0/0 | 2485 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0021 | 0/0 | 2485 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0022 | 0/0 | 2485 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| 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 | 0/0 | 7458 | 50 | 0 | 12 | 31 | 5 | 2 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0002 | 0/1 | 7458 | 34 | 22 | 6 | 5 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0003 | 0/0 | 7458 | 33 | 2 | 8 | 19 | 2 | 2 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0004 | 1/0 | 7458 | 26 | 2 | 4 | 17 | 2 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0005 | 0/0 | 7458 | 8 | 0 | 6 | 1 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0006 | 0/0 | 7458 | 6 | 6 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0007 | 0/0 | 7458 | 4 | 4 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0008 | 0/0 | 7458 | 4 | 0 | 0 | 4 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0009 | 0/0 | 7458 | 3 | 0 | 1 | 2 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0010 | 0/0 | 7458 | 3 | 3 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0011 | 0/0 | 7458 | 3 | 0 | 0 | 3 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0012 | 0/0 | 7458 | 2 | 0 | 0 | 2 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0013 | 0/0 | 7458 | 2 | 1 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0014 | 0/0 | 7458 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0015 | 0/0 | 7458 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0016 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0017 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0018 | 0/0 | 7458 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0019 | 0/0 | 7458 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0020 | 0/0 | 7458 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0021 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0022 | 0/0 | 7458 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0023 | 0/0 | 7458 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0024 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0025 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0026 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0027 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0028 | 0/0 | 7458 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0029 | 0/0 | 7458 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0030 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0031 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| c0032 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| 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 | 1/1 | 1091 | 88 | 21 | 16 | 44 | 2 | 3 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| t0002 | 0/0 | 1091 | 74 | 8 | 18 | 39 | 7 | 2 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| t0003 | 0/0 | 1091 | 16 | 15 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| t0004 | 0/0 | 1091 | 9 | 3 | 4 | 1 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| t0005 | 0/0 | 1091 | 6 | 3 | 2 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| t0006 | 0/0 | 1091 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| t0007 | 0/0 | 1091 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| t0008 | 0/0 | 1091 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| t0009 | 0/0 | 1091 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| t0010 | 0/0 | 1091 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| 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 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003 | 0/0 | 7458 | 33 | 2 | 8 | 19 | 2 | 2 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0001c0004 | 1/0 | 7458 | 26 | 2 | 4 | 17 | 2 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0001c0017 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0001c0018 | 0/0 | 7458 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0001c0027 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0002c0001 | 0/0 | 7458 | 50 | 0 | 12 | 31 | 5 | 2 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0002c0011 | 0/0 | 7458 | 3 | 0 | 0 | 3 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003c0002 | 0/1 | 7458 | 34 | 22 | 6 | 5 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003c0006 | 0/0 | 7458 | 6 | 6 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003c0009 | 0/0 | 7458 | 3 | 0 | 1 | 2 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0004c0005 | 0/0 | 7458 | 8 | 0 | 6 | 1 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0004c0028 | 0/0 | 7458 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0005c0008 | 0/0 | 7458 | 4 | 0 | 0 | 4 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0006c0010 | 0/0 | 7458 | 3 | 3 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0006c0025 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0007c0007 | 0/0 | 7458 | 4 | 4 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0008c0014 | 0/0 | 7458 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0008c0032 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0009c0012 | 0/0 | 7458 | 2 | 0 | 0 | 2 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0010c0013 | 0/0 | 7458 | 2 | 1 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0011c0015 | 0/0 | 7458 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0012c0016 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0013c0029 | 0/0 | 7458 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0014c0026 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0015c0021 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0016c0019 | 0/0 | 7458 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0017c0022 | 0/0 | 7458 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0018c0023 | 0/0 | 7458 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0019c0024 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0020c0020 | 0/0 | 7458 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0021c0030 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0022c0031 | 0/0 | 7458 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0001 | 0/0 | 8548 | 32 | 1 | 8 | 19 | 2 | 2 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0001c0003t0002 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0001c0004t0001 | 1/0 | 8548 | 21 | 2 | 4 | 14 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0001c0004t0002 | 0/0 | 8548 | 3 | 0 | 0 | 1 | 2 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0001c0004t0007 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0001c0004t0008 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0001c0017t0001 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0001c0018t0001 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0001c0027t0001 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0002c0001t0002 | 0/0 | 8548 | 50 | 0 | 12 | 31 | 5 | 2 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0002c0011t0001 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0002c0011t0002 | 0/0 | 8548 | 2 | 0 | 0 | 2 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003c0002t0001 | 0/1 | 8548 | 23 | 14 | 3 | 5 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003c0002t0002 | 0/0 | 8548 | 8 | 6 | 2 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003c0002t0003 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003c0002t0005 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003c0002t0009 | 0/0 | 8548 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003c0006t0001 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003c0006t0003 | 0/0 | 8548 | 4 | 4 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003c0006t0010 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003c0009t0001 | 0/0 | 8548 | 2 | 0 | 0 | 2 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0003c0009t0002 | 0/0 | 8548 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0004c0005t0004 | 0/0 | 8548 | 6 | 0 | 4 | 1 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0004c0005t0005 | 0/0 | 8548 | 2 | 0 | 2 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0004c0028t0005 | 0/0 | 8548 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0005c0008t0002 | 0/0 | 8548 | 4 | 0 | 0 | 4 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0006c0010t0003 | 0/0 | 8548 | 3 | 3 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0006c0025t0003 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0007c0007t0004 | 0/0 | 8548 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0007c0007t0005 | 0/0 | 8548 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0008c0014t0003 | 0/0 | 8548 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0008c0032t0003 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0009c0012t0001 | 0/0 | 8548 | 2 | 0 | 0 | 2 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0010c0013t0003 | 0/0 | 8548 | 2 | 1 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0011c0015t0001 | 0/0 | 8548 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0012c0016t0006 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0013c0029t0002 | 0/0 | 8548 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0014c0026t0003 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0015c0021t0001 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0016c0019t0002 | 0/0 | 8548 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0017c0022t0002 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0018c0023t0002 | 0/0 | 8548 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0019c0024t0004 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0020c0020t0001 | 0/0 | 8548 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0021c0030t0002 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| a0022c0031t0003 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | copy fasta | chr4 | 86589315 | 86820161 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0003t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0004t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0017t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0018t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0001c0027t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0011t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0011t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0002c0011t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0002t0009g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0006t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0006t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0006t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0006t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0006t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0006t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0009t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0009t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0003c0009t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0004c0005t0004g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0004c0005t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0004c0005t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0004c0005t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0004c0005t0004g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0004c0005t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0004c0005t0005g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0004c0005t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0004c0028t0005g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0005c0008t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0005c0008t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0005c0008t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0005c0008t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0006c0010t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0006c0010t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0006c0010t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0006c0025t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0007c0007t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0007c0007t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0007c0007t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0007c0007t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0008c0014t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0008c0014t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0008c0032t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0009c0012t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0009c0012t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0010c0013t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0010c0013t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0011c0015t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0012c0016t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0013c0029t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0014c0026t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0015c0021t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0016c0019t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0017c0022t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0018c0023t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0019c0024t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0020c0020t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0021c0030t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| a0022c0031t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0001 | t0002 | g0155 | EUR | GBR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0079 | EUR | GBR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00280 | hp1 | a0002 | c0001 | t0002 | g0131 | EUR | FIN | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0083 | EUR | FIN | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00423 | hp1 | a0002 | c0001 | t0002 | g0111 | EAS | CHS | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | CHS | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00438 | hp1 | a0001 | c0004 | t0001 | g0056 | EAS | CHS | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00438 | hp2 | a0009 | c0012 | t0001 | g0191 | EAS | CHS | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00609 | hp1 | a0001 | c0004 | t0001 | g0074 | EAS | CHS | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00609 | hp2 | a0002 | c0001 | t0002 | g0158 | EAS | CHS | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00639 | hp1 | a0003 | c0002 | t0002 | g0007 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00639 | hp2 | a0002 | c0001 | t0002 | g0147 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00642 | hp1 | a0011 | c0015 | t0001 | g0041 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00642 | hp2 | a0018 | c0023 | t0002 | g0143 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00738 | hp1 | a0002 | c0001 | t0002 | g0146 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG00738 | hp2 | a0004 | c0005 | t0005 | g0076 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01071 | hp1 | a0003 | c0002 | t0001 | g0186 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01071 | hp2 | a0002 | c0001 | t0002 | g0107 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01074 | hp1 | a0002 | c0001 | t0002 | g0154 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0090 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01081 | hp1 | a0003 | c0002 | t0002 | g0184 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0044 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01099 | hp1 | a0004 | c0005 | t0005 | g0084 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01099 | hp2 | a0003 | c0009 | t0002 | g0144 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01106 | hp1 | a0002 | c0001 | t0002 | g0119 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01106 | hp2 | a0001 | c0004 | t0001 | g0087 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0080 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01168 | hp2 | a0002 | c0001 | t0002 | g0109 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01175 | hp2 | a0004 | c0005 | t0004 | g0001 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01192 | hp1 | a0004 | c0005 | t0004 | g0003 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0081 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01243 | hp1 | a0010 | c0013 | t0003 | g0011 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01243 | hp2 | a0003 | c0002 | t0001 | g0178 | AMR | PUR | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01346 | hp1 | a0004 | c0005 | t0004 | g0002 | AMR | CLM | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01346 | hp2 | a0013 | c0029 | t0002 | g0145 | AMR | CLM | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01361 | hp1 | a0002 | c0001 | t0002 | g0141 | AMR | CLM | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0057 | AMR | CLM | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01496 | hp1 | a0003 | c0002 | t0001 | g0183 | AMR | CLM | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01496 | hp2 | a0002 | c0001 | t0002 | g0116 | AMR | CLM | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01516 | hp1 | a0004 | c0028 | t0005 | g0077 | EUR | IBS | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01516 | hp2 | a0002 | c0001 | t0002 | g0129 | EUR | IBS | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01517 | hp1 | a0002 | c0001 | t0002 | g0130 | EUR | IBS | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01517 | hp2 | a0001 | c0004 | t0002 | g0046 | EUR | IBS | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01891 | hp1 | a0003 | c0006 | t0003 | g0022 | AFR | ACB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01891 | hp2 | a0015 | c0021 | t0001 | g0042 | AFR | ACB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01978 | hp1 | a0016 | c0019 | t0002 | g0045 | AMR | PEL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01978 | hp2 | a0002 | c0001 | t0002 | g0117 | AMR | PEL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01981 | hp1 | a0003 | c0002 | t0009 | g0188 | AMR | PEL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01981 | hp2 | a0001 | c0004 | t0001 | g0071 | AMR | PEL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0093 | AMR | PEL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01993 | hp2 | a0002 | c0001 | t0002 | g0125 | AMR | PEL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02015 | hp1 | a0001 | c0018 | t0001 | g0078 | EAS | KHV | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02015 | hp2 | a0009 | c0012 | t0001 | g0185 | EAS | KHV | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02056 | hp1 | a0002 | c0001 | t0002 | g0164 | EAS | KHV | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0068 | EAS | KHV | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02083 | hp1 | a0001 | c0004 | t0001 | g0055 | EAS | KHV | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02083 | hp2 | a0002 | c0001 | t0002 | g0121 | EAS | KHV | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02129 | hp1 | a0001 | c0004 | t0008 | g0049 | EAS | KHV | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02129 | hp2 | a0002 | c0001 | t0002 | g0153 | EAS | KHV | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0094 | EAS | KHV | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02135 | hp2 | a0002 | c0001 | t0002 | g0137 | EAS | KHV | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02145 | hp1 | a0003 | c0002 | t0001 | g0098 | AFR | ACB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02145 | hp2 | a0022 | c0031 | t0003 | g0027 | AFR | ACB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02148 | hp1 | a0002 | c0001 | t0002 | g0122 | AMR | PEL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02148 | hp2 | a0001 | c0004 | t0001 | g0073 | AMR | PEL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02273 | hp1 | a0001 | c0004 | t0001 | g0181 | AMR | PEL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02273 | hp2 | a0002 | c0001 | t0002 | g0115 | AMR | PEL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02280 | hp1 | a0007 | c0007 | t0005 | g0179 | AFR | ACB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02280 | hp2 | a0001 | c0017 | t0001 | g0043 | AFR | ACB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02451 | hp1 | a0003 | c0006 | t0003 | g0023 | AFR | ACB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02451 | hp2 | a0003 | c0002 | t0001 | g0099 | AFR | ACB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02615 | hp1 | a0003 | c0002 | t0001 | g0171 | AFR | GWD | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02615 | hp2 | a0010 | c0013 | t0003 | g0018 | AFR | GWD | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02622 | hp1 | a0003 | c0002 | t0001 | g0097 | AFR | GWD | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02622 | hp2 | a0003 | c0002 | t0001 | g0172 | AFR | GWD | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02647 | hp1 | a0003 | c0002 | t0001 | g0168 | AFR | GWD | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0050 | AFR | GWD | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02717 | hp1 | a0008 | c0014 | t0003 | g0026 | AFR | GWD | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02717 | hp2 | a0007 | c0007 | t0004 | g0132 | AFR | GWD | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0060 | SAS | PJL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02735 | hp2 | a0004 | c0005 | t0004 | g0004 | SAS | PJL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02818 | hp1 | a0008 | c0014 | t0003 | g0025 | AFR | GWD | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02818 | hp2 | a0019 | c0024 | t0004 | g0008 | AFR | GWD | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02970 | hp1 | a0003 | c0006 | t0003 | g0024 | AFR | ESN | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02970 | hp2 | a0003 | c0002 | t0001 | g0174 | AFR | ESN | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02976 | hp1 | a0021 | c0030 | t0002 | g0013 | AFR | ESN | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02976 | hp2 | a0003 | c0002 | t0001 | g0096 | AFR | ESN | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03041 | hp1 | a0003 | c0002 | t0002 | g0017 | AFR | GWD | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03041 | hp2 | a0006 | c0025 | t0003 | g0020 | AFR | GWD | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03098 | hp1 | a0003 | c0002 | t0002 | g0010 | AFR | MSL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03098 | hp2 | a0014 | c0026 | t0003 | g0019 | AFR | MSL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03130 | hp1 | a0003 | c0002 | t0002 | g0016 | AFR | ESN | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03130 | hp2 | a0003 | c0002 | t0001 | g0103 | AFR | ESN | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03139 | hp1 | a0006 | c0010 | t0003 | g0195 | AFR | ESN | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03139 | hp2 | a0003 | c0002 | t0005 | g0169 | AFR | ESN | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03225 | hp1 | a0003 | c0006 | t0001 | g0030 | AFR | MSL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03225 | hp2 | a0007 | c0007 | t0004 | g0167 | AFR | MSL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03453 | hp1 | a0003 | c0002 | t0001 | g0173 | AFR | MSL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03453 | hp2 | a0006 | c0010 | t0003 | g0194 | AFR | MSL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03516 | hp1 | a0003 | c0006 | t0010 | g0029 | AFR | ESN | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03516 | hp2 | a0003 | c0002 | t0001 | g0170 | AFR | ESN | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03579 | hp1 | a0008 | c0032 | t0003 | g0028 | AFR | MSL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG03579 | hp2 | a0003 | c0002 | t0001 | g0101 | AFR | MSL | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0065 | SAS | STU | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG04115 | hp2 | a0002 | c0001 | t0002 | g0104 | SAS | STU | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG04228 | hp1 | a0002 | c0001 | t0002 | g0166 | SAS | STU | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG04228 | hp2 | a0020 | c0020 | t0001 | g0054 | SAS | STU | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | YRI | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18522 | hp2 | a0003 | c0002 | t0001 | g0100 | AFR | YRI | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18612 | hp1 | a0002 | c0001 | t0002 | g0162 | EAS | CHB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18612 | hp2 | a0003 | c0002 | t0001 | g0192 | EAS | CHB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18906 | hp1 | a0012 | c0016 | t0006 | g0198 | AFR | YRI | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0176 | AFR | YRI | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18943 | hp1 | a0001 | c0003 | t0001 | g0058 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18943 | hp2 | a0002 | c0001 | t0002 | g0118 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18944 | hp1 | a0001 | c0004 | t0001 | g0069 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18944 | hp2 | a0002 | c0001 | t0002 | g0136 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18947 | hp1 | a0001 | c0004 | t0001 | g0053 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18947 | hp2 | a0002 | c0001 | t0002 | g0163 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18948 | hp1 | a0002 | c0001 | t0002 | g0134 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18948 | hp2 | a0003 | c0009 | t0001 | g0102 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0035 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18951 | hp2 | a0002 | c0001 | t0002 | g0159 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18953 | hp1 | a0002 | c0011 | t0002 | g0124 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18953 | hp2 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18954 | hp1 | a0002 | c0001 | t0002 | g0106 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18954 | hp2 | a0003 | c0002 | t0001 | g0180 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18959 | hp1 | a0002 | c0011 | t0001 | g0113 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18959 | hp2 | a0001 | c0004 | t0001 | g0072 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0037 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18967 | hp2 | a0002 | c0001 | t0002 | g0120 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18968 | hp1 | a0002 | c0001 | t0002 | g0156 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18968 | hp2 | a0003 | c0002 | t0001 | g0190 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18969 | hp1 | a0004 | c0005 | t0004 | g0009 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18969 | hp2 | a0002 | c0011 | t0002 | g0112 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18971 | hp1 | a0003 | c0002 | t0001 | g0091 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18974 | hp1 | a0002 | c0001 | t0002 | g0157 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0088 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0051 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18975 | hp2 | a0002 | c0001 | t0002 | g0108 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18982 | hp1 | a0001 | c0004 | t0001 | g0075 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18982 | hp2 | a0017 | c0022 | t0002 | g0114 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18984 | hp1 | a0002 | c0001 | t0002 | g0165 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18985 | hp1 | a0002 | c0001 | t0002 | g0139 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18991 | hp1 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18991 | hp2 | a0002 | c0001 | t0002 | g0160 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18992 | hp1 | a0002 | c0001 | t0002 | g0138 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18992 | hp2 | a0001 | c0003 | t0001 | g0092 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18994 | hp1 | a0002 | c0001 | t0002 | g0149 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA18994 | hp2 | a0001 | c0004 | t0001 | g0032 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0064 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19002 | hp2 | a0002 | c0001 | t0002 | g0140 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19003 | hp1 | a0001 | c0004 | t0007 | g0067 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19003 | hp2 | a0002 | c0001 | t0002 | g0135 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19007 | hp2 | a0005 | c0008 | t0002 | g0128 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19011 | hp1 | a0002 | c0001 | t0002 | g0148 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19011 | hp2 | a0003 | c0002 | t0001 | g0189 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19043 | hp1 | a0003 | c0002 | t0003 | g0193 | AFR | LWK | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19043 | hp2 | a0001 | c0027 | t0001 | g0031 | AFR | LWK | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19056 | hp1 | a0001 | c0004 | t0002 | g0126 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19056 | hp2 | a0002 | c0001 | t0002 | g0133 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0038 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19057 | hp2 | a0002 | c0001 | t0002 | g0110 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19058 | hp1 | a0005 | c0008 | t0002 | g0150 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19058 | hp2 | a0001 | c0004 | t0001 | g0052 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19063 | hp1 | a0003 | c0009 | t0001 | g0040 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19063 | hp2 | a0001 | c0003 | t0001 | g0059 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19066 | hp1 | a0001 | c0004 | t0001 | g0070 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19066 | hp2 | a0002 | c0001 | t0002 | g0151 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19068 | hp1 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19068 | hp2 | a0002 | c0001 | t0002 | g0127 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19078 | hp1 | a0001 | c0004 | t0001 | g0086 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19078 | hp2 | a0002 | c0001 | t0002 | g0123 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19079 | hp1 | a0002 | c0001 | t0002 | g0105 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19079 | hp2 | a0001 | c0004 | t0001 | g0048 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0089 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19080 | hp2 | a0005 | c0008 | t0002 | g0152 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19089 | hp1 | a0005 | c0008 | t0002 | g0161 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19089 | hp2 | a0001 | c0004 | t0001 | g0036 | EAS | JPT | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19240 | hp1 | a0007 | c0007 | t0005 | g0175 | AFR | YRI | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA19240 | hp2 | a0003 | c0002 | t0002 | g0012 | AFR | YRI | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA20752 | hp1 | a0002 | c0001 | t0002 | g0142 | EUR | TSI | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA20752 | hp2 | a0001 | c0004 | t0002 | g0047 | EUR | TSI | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0082 | AMR | CLM | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG01123 | hp2 | a0004 | c0005 | t0004 | g0005 | AMR | CLM | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02486 | hp1 | a0006 | c0010 | t0003 | g0196 | AFR | ACB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02486 | hp2 | a0003 | c0002 | t0002 | g0015 | AFR | ACB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02559 | hp1 | a0003 | c0006 | t0003 | g0021 | AFR | ACB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0062 | AFR | ACB | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA20300 | hp1 | a0003 | c0002 | t0002 | g0014 | AFR | USA | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| NA20300 | hp2 | a0003 | c0002 | t0001 | g0197 | AFR | USA | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0002 | t0001 | g0187 | REF | REF | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0001 | g0177 | REF | REF | PTPN13_chr4_86589315_86820161 | PTPN13 | chr4 | 86589315 | 86820161 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:86672517
|
C | G | 2 | a0008a0022 | 4 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.268C>G | p.Leu90Val | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/48 | 748/8548 | 268/7458 | 90/2485 | chr4 | 86672517 | ||
| chr4:86701465
|
A | G | 1 | a0021 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.859A>G | p.Ile287Val | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/48 | 1339/8548 | 859/7458 | 287/2485 | chr4 | 86701465 | ||
| chr4:86701571
|
G | A | 1 | a0011 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.965G>A | p.Arg322His | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/48 | 1445/8548 | 965/7458 | 322/2485 | chr4 | 86701571 | ||
| chr4:86701574
|
G | A | 1 | a0012 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.968G>A | p.Arg323His | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/48 | 1448/8548 | 968/7458 | 323/2485 | chr4 | 86701574 | ||
| chr4:86701618
|
A | G | 1 | a0013 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.1012A>G | p.Arg338Gly | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/48 | 1492/8548 | 1012/7458 | 338/2485 | chr4 | 86701618 | ||
| chr4:86701688
|
C | T | 1 | a0005 | 4 | NA19007.hp2 NA19058.hp1 NA19080.hp2 others(1): Show |
missense_variant | MODERATE | c.1082C>T | p.Pro361Leu | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/48 | 1562/8548 | 1082/7458 | 361/2485 | chr4 | 86701688 | ||
| chr4:86701703
|
G | A | 1 | a0009 | 2 | HG00438.hp2 HG02015.hp2 |
missense_variant | MODERATE | c.1097G>A | p.Arg366Gln | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/48 | 1577/8548 | 1097/7458 | 366/2485 | chr4 | 86701703 | ||
| chr4:86722245
|
A | T | 1 | a0010 | 2 | HG01243.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.1419A>T | p.Leu473Phe | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/48 | 1899/8548 | 1419/7458 | 473/2485 | chr4 | 86722245 | ||
| chr4:86762928
|
A | G | 1 | a0020 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.3755A>G | p.Glu1252Gly | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 24/48 | 4235/8548 | 3755/7458 | 1252/2485 | chr4 | 86762928 | ||
| chr4:86763081
|
A | G | 1 | a0019 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.3908A>G | p.Lys1303Arg | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 24/48 | 4388/8548 | 3908/7458 | 1303/2485 | chr4 | 86763081 | ||
| chr4:86764643
|
T | G | 2 | a0004a0012 | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
missense_variant | MODERATE | c.4068T>G | p.Phe1356Leu | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 25/48 | 4548/8548 | 4068/7458 | 1356/2485 | chr4 | 86764643 | ||
| chr4:86769845
|
A | G | 4 | a0002a0005a0017others(1): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
missense_variant | MODERATE | c.4566A>G | p.Ile1522Met | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 29/48 | 5046/8548 | 4566/7458 | 1522/2485 | chr4 | 86769845 | ||
| chr4:86769927
|
G | A | 1 | a0017 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.4648G>A | p.Val1550Ile | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 29/48 | 5128/8548 | 4648/7458 | 1550/2485 | chr4 | 86769927 | ||
| chr4:86771240
|
G | A | 1 | a0004 | 9 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(6): Show |
missense_variant | MODERATE | c.4873G>A | p.Glu1625Lys | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 31/48 | 5353/8548 | 4873/7458 | 1625/2485 | chr4 | 86771240 | ||
| chr4:86772839
|
T | C | 1 | a0006 | 4 | HG02486.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
missense_variant | MODERATE | c.5230T>C | p.Ser1744Pro | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 32/48 | 5710/8548 | 5230/7458 | 1744/2485 | chr4 | 86772839 | ||
| chr4:86785353
|
T | G | 14 | a0002a0003a0004others(11): Show | 129 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(126): Show |
missense_variant | MODERATE | c.6241T>G | p.Tyr2081Asp | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 39/48 | 6721/8548 | 6241/7458 | 2081/2485 | chr4 | 86785353 | ||
| chr4:86799180
|
A | G | 1 | a0010 | 2 | HG01243.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.6481A>G | p.Thr2161Ala | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/48 | 6961/8548 | 6481/7458 | 2161/2485 | chr4 | 86799180 | ||
| chr4:86803817
|
G | A | 1 | a0015 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.6614G>A | p.Arg2205Gln | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 43/48 | 7094/8548 | 6614/7458 | 2205/2485 | chr4 | 86803817 | ||
| chr4:86807652
|
A | G | 1 | a0014 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.6838A>G | p.Ile2280Val | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/48 | 7318/8548 | 6838/7458 | 2280/2485 | chr4 | 86807652 | ||
| chr4:86811068
|
G | A | 1 | a0016 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.7322G>A | p.Arg2441His | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/48 | 7802/8548 | 7322/7458 | 2441/2485 | chr4 | 86811068 | ||
| chr4:86814465
|
A | G | 2 | a0007a0019 | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
missense_variant | MODERATE | c.7372A>G | p.Ile2458Val | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 48/48 | 7852/8548 | 7372/7458 | 2458/2485 | chr4 | 86814465 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:86701635
|
A | G | 1 | a0004c0028 | 1 | HG01516.hp1 | synonymous_variant | LOW | c.1029A>G | p.Arg343Arg | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/48 | 1509/8548 | 1029/7458 | 343/2485 | chr4 | 86701635 | ||
| chr4:86701671
|
C | A | 1 | a0001c0017 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.1065C>A | p.Gly355Gly | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/48 | 1545/8548 | 1065/7458 | 355/2485 | chr4 | 86701671 | ||
| chr4:86732633
|
C | T | 1 | a0001c0027 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1725C>T | p.Asn575Asn | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 12/48 | 2205/8548 | 1725/7458 | 575/2485 | chr4 | 86732633 | ||
| chr4:86750597
|
A | G | 6 | a0003c0006a0006c0025a0008c0014others(3): Show | 13 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
synonymous_variant | LOW | c.2778A>G | p.Ser926Ser | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 18/48 | 3258/8548 | 2778/7458 | 926/2485 | chr4 | 86750597 | ||
| chr4:86762878
|
A | G | 23 | a0001c0003a0001c0017a0002c0001others(20): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
synonymous_variant | LOW | c.3705A>G | p.Pro1235Pro | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 24/48 | 4185/8548 | 3705/7458 | 1235/2485 | chr4 | 86762878 | ||
| chr4:86771455
|
A | G | 1 | a0021c0030 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.5088A>G | p.Ala1696Ala | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 31/48 | 5568/8548 | 5088/7458 | 1696/2485 | chr4 | 86771455 | ||
| chr4:86775308
|
G | A | 1 | a0002c0011 | 3 | NA18953.hp1 NA18959.hp1 NA18969.hp2 |
synonymous_variant | LOW | c.5646G>A | p.Pro1882Pro | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 34/48 | 6126/8548 | 5646/7458 | 1882/2485 | chr4 | 86775308 | ||
| chr4:86775317
|
A | G | 5 | a0004c0005a0004c0028a0007c0007others(2): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
synonymous_variant | LOW | c.5655A>G | p.Thr1885Thr | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 34/48 | 6135/8548 | 5655/7458 | 1885/2485 | chr4 | 86775317 | ||
| chr4:86775323
|
G | A | 5 | a0004c0005a0004c0028a0007c0007others(2): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
synonymous_variant | LOW | c.5661G>A | p.Thr1887Thr | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 34/48 | 6141/8548 | 5661/7458 | 1887/2485 | chr4 | 86775323 | ||
| chr4:86803779
|
C | T | 1 | a0008c0014 | 2 | HG02717.hp1 HG02818.hp1 |
synonymous_variant | LOW | c.6576C>T | p.Tyr2192Tyr | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 43/48 | 7056/8548 | 6576/7458 | 2192/2485 | chr4 | 86803779 | ||
| chr4:86803812
|
C | T | 1 | a0012c0016 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.6609C>T | p.Val2203Val | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 43/48 | 7089/8548 | 6609/7458 | 2203/2485 | chr4 | 86803812 | ||
| chr4:86809903
|
G | A | 1 | a0001c0018 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.7218G>A | p.Thr2406Thr | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 46/48 | 7698/8548 | 7218/7458 | 2406/2485 | chr4 | 86809903 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:86594465
|
G | A | 1 | a0012c0016t0006 | 1 | NA18906.hp1 | 5_prime_UTR_variant | MODIFIER | c.-330G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/48 | 40792 | chr4 | 86594465 | |||||
| chr4:86594500
|
C | T | 1 | a0012c0016t0006 | 1 | NA18906.hp1 | 5_prime_UTR_variant | MODIFIER | c.-295C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/48 | 40757 | chr4 | 86594500 | |||||
| chr4:86594637
|
A | C | 16 | a0001c0003t0002a0001c0004t0002a0002c0001t0002others(13): Show | 84 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(81): Show |
5_prime_UTR_variant | MODIFIER | c.-158A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/48 | 40620 | chr4 | 86594637 | |||||
| chr4:86594679
|
T | A | 25 | a0001c0003t0002a0001c0004t0002a0002c0001t0002others(22): Show | 100 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(97): Show |
5_prime_UTR_variant | MODIFIER | c.-116T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/48 | 40578 | chr4 | 86594679 | |||||
| chr4:86814903
|
A | G | 1 | a0003c0006t0010 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 48/48 | 352 | chr4 | 86814903 | |||||
| chr4:86815080
|
T | C | 1 | a0001c0004t0007 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*529T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 48/48 | 529 | chr4 | 86815080 | |||||
| chr4:86815138
|
C | T | 1 | a0003c0002t0009 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*587C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 48/48 | 587 | chr4 | 86815138 | |||||
| chr4:86815154
|
A | C | 7 | a0003c0002t0005a0004c0005t0004a0004c0005t0005others(4): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*603A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 48/48 | 603 | chr4 | 86815154 | |||||
| chr4:86815156
|
C | A | 1 | a0001c0004t0008 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*605C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 48/48 | 605 | chr4 | 86815156 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:86594917
|
C | T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6+128C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86594917 | ||||||
| chr4:86594972
|
G | A | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+183G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86594972 | ||||||
| chr4:86595073
|
G | T | 1 | a0003c0002t0001g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-6+284G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86595073 | ||||||
| chr4:86595573
|
A | G | 4 | a0003c0002t0003g0193a0006c0010t0003g0194a0006c0010t0003g0195others(1): Show | 4 | HG02486.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+784A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86595573 | ||||||
| chr4:86595808
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6+1019G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86595808 | ||||||
| chr4:86595811
|
T | C | 2 | a0004c0005t0004g0009a0012c0016t0006g0198 | 2 | NA18906.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-6+1022T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86595811 | ||||||
| chr4:86596016
|
G | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+1227G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86596016 | ||||||
| chr4:86596144
|
A | C | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+1355A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86596144 | ||||||
| chr4:86596456
|
T | G | 172 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.-6+1667T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86596456 | ||||||
| chr4:86596653
|
T | C | 1 | a0003c0002t0001g0168 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-6+1864T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86596653 | ||||||
| chr4:86596756
|
A | G | 1 | a0007c0007t0004g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-6+1967A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86596756 | ||||||
| chr4:86596793
|
T | C | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-6+2004T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86596793 | ||||||
| chr4:86596997
|
G | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+2208G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86596997 | ||||||
| chr4:86597036
|
C | G | 64 | a0001c0004t0002g0126a0002c0001t0002g0104a0002c0001t0002g0105others(61): Show | 64 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-6+2247C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86597036 | ||||||
| chr4:86597090
|
G | C | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+2301G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86597090 | ||||||
| chr4:86597166
|
C | CT | 30 | a0001c0003t0001g0182a0001c0003t0002g0006a0001c0004t0001g0181others(27): Show | 30 | HG00438.hp2 HG00639.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-6+2391dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86597166 | |||||
| chr4:86597409
|
G | GTTTAT | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+2629_-6+2633dup others(5): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86597409 | |||||
| chr4:86597667
|
G | A | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+2878G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86597667 | ||||||
| chr4:86597791
|
A | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+3002A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86597791 | ||||||
| chr4:86597848
|
A | G | 1 | a0003c0002t0001g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-6+3059A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86597848 | ||||||
| chr4:86597920
|
G | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-6+3131G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86597920 | ||||||
| chr4:86597980
|
G | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-6+3191G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86597980 | ||||||
| chr4:86598151
|
C | CT | 16 | a0001c0003t0001g0088a0001c0003t0001g0089a0001c0003t0001g0090others(13): Show | 16 | HG00639.hp1 HG01074.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.-6+3375dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86598151 | |||||
| chr4:86598166
|
A | G | 1 | a0003c0002t0001g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-6+3377A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86598166 | ||||||
| chr4:86598356
|
T | G | 93 | a0001c0003t0002g0006a0001c0004t0002g0126a0002c0001t0002g0104others(90): Show | 93 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-6+3567T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86598356 | ||||||
| chr4:86598505
|
A | ACACT | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+3718_-6+3719ins others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86598505 | |||||
| chr4:86598530
|
T | G | 1 | a0010c0013t0003g0011 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-6+3741T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86598530 | ||||||
| chr4:86598595
|
G | A | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+3806G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86598595 | ||||||
| chr4:86599075
|
T | C | 1 | a0002c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-6+4286T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86599075 | ||||||
| chr4:86599143
|
T | C | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+4354T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86599143 | ||||||
| chr4:86599610
|
C | CT | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+4823dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86599610 | |||||
| chr4:86599633
|
A | G | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-6+4844A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86599633 | ||||||
| chr4:86599934
|
T | G | 64 | a0001c0004t0002g0126a0002c0001t0002g0104a0002c0001t0002g0105others(61): Show | 64 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-6+5145T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86599934 | ||||||
| chr4:86599971
|
C | T | 1 | a0001c0004t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-6+5182C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86599971 | ||||||
| chr4:86600009
|
C | A | 89 | a0001c0003t0002g0006a0001c0004t0002g0126a0002c0001t0002g0104others(86): Show | 89 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-6+5220C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86600009 | ||||||
| chr4:86600285
|
A | G | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-6+5496A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86600285 | ||||||
| chr4:86600288
|
C | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-6+5499C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86600288 | ||||||
| chr4:86600393
|
CCTT | C | 8 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6+5608_-6+5610del others(3): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86600393 | |||||
| chr4:86600417
|
T | C | 1 | a0004c0005t0004g0001 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-6+5628T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86600417 | ||||||
| chr4:86600432
|
C | CT | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+5669dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86600432 | |||||
| chr4:86600432
|
CT | C | 91 | a0001c0003t0001g0034a0001c0003t0001g0035a0001c0003t0001g0037others(88): Show | 91 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-6+5669delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86600432 | |||||
| chr4:86600432
|
CTT | C | 81 | a0001c0003t0001g0033a0001c0004t0001g0032a0001c0004t0002g0126others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.-6+5668_-6+5669del others(2): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86600432 | |||||
| chr4:86600520
|
C | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+5731C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86600520 | ||||||
| chr4:86600614
|
T | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6+5825T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86600614 | ||||||
| chr4:86600637
|
A | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+5848A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86600637 | ||||||
| chr4:86600644
|
A | G | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-6+5855A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86600644 | ||||||
| chr4:86600999
|
T | A | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+6210T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86600999 | ||||||
| chr4:86601258
|
G | A | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+6469G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86601258 | ||||||
| chr4:86601298
|
C | A | 25 | a0001c0004t0002g0126a0002c0001t0002g0105a0002c0001t0002g0106others(22): Show | 25 | HG00423.hp1 HG01071.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-6+6509C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86601298 | ||||||
| chr4:86601681
|
A | G | 3 | a0006c0010t0003g0194a0006c0010t0003g0195a0006c0010t0003g0196 | 3 | HG02486.hp1 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-6+6892A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86601681 | ||||||
| chr4:86601708
|
A | G | 1 | a0002c0001t0002g0162 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-6+6919A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86601708 | ||||||
| chr4:86602241
|
G | A | 64 | a0001c0004t0002g0126a0002c0001t0002g0104a0002c0001t0002g0105others(61): Show | 64 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-6+7452G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86602241 | ||||||
| chr4:86602496
|
C | CTG | 89 | a0001c0003t0002g0006a0001c0004t0002g0126a0002c0001t0002g0104others(86): Show | 89 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-6+7707_-6+7708ins others(2): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86602496 | ||||||
| chr4:86602526
|
G | T | 1 | a0008c0032t0003g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-6+7737G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86602526 | ||||||
| chr4:86602577
|
C | G | 1 | a0004c0005t0005g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-6+7788C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86602577 | ||||||
| chr4:86602694
|
AT | A | 10 | a0001c0003t0002g0006a0003c0002t0002g0007a0003c0002t0002g0012others(7): Show | 10 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.-6+7921delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86602694 | |||||
| chr4:86602698
|
T | G | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+7909T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86602698 | ||||||
| chr4:86602724
|
A | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+7935A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86602724 | ||||||
| chr4:86602781
|
C | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+7992C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86602781 | ||||||
| chr4:86602798
|
C | T | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+8009C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86602798 | ||||||
| chr4:86602858
|
C | G | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-6+8069C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86602858 | ||||||
| chr4:86603133
|
A | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+8344A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86603133 | ||||||
| chr4:86603254
|
C | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+8465C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86603254 | ||||||
| chr4:86603270
|
A | G | 2 | a0005c0008t0002g0128a0005c0008t0002g0161 | 2 | NA19007.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.-6+8481A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86603270 | ||||||
| chr4:86603272
|
C | CA | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+8483_-6+8484ins others(1): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86603272 | ||||||
| chr4:86603278
|
C | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+8489C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86603278 | ||||||
| chr4:86603281
|
G | GAGGACAA others(6): Show |
8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+8492_-6+8493ins others(13): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86603281 | ||||||
| chr4:86603291
|
C | T | 5 | a0001c0003t0001g0079a0001c0003t0001g0080a0001c0003t0001g0081others(2): Show | 5 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+8502C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86603291 | ||||||
| chr4:86603545
|
C | G | 1 | a0007c0007t0004g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-6+8756C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86603545 | ||||||
| chr4:86603591
|
G | A | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+8802G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86603591 | ||||||
| chr4:86603700
|
G | A | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+8911G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86603700 | ||||||
| chr4:86603810
|
A | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6+9021A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86603810 | ||||||
| chr4:86603998
|
GTTA | G | 3 | a0001c0003t0002g0006a0003c0002t0002g0007a0019c0024t0004g0008 | 3 | HG00639.hp1 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-6+9212_-6+9214del others(3): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86603998 | |||||
| chr4:86604099
|
G | A | 2 | a0001c0003t0001g0088a0001c0003t0001g0089 | 2 | NA18974.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-6+9310G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86604099 | ||||||
| chr4:86604149
|
C | A | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+9360C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86604149 | ||||||
| chr4:86604211
|
C | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+9422C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86604211 | ||||||
| chr4:86604323
|
T | C | 1 | a0003c0002t0005g0169 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-6+9534T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86604323 | ||||||
| chr4:86604613
|
C | A | 1 | a0001c0003t0001g0034 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-6+9824C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86604613 | ||||||
| chr4:86605070
|
A | T | 1 | a0001c0018t0001g0078 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-6+10281A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86605070 | ||||||
| chr4:86605137
|
T | A | 1 | a0004c0005t0004g0002 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-6+10348T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86605137 | ||||||
| chr4:86605140
|
G | A | 6 | a0001c0003t0001g0035a0001c0003t0001g0037a0001c0003t0001g0038others(3): Show | 6 | NA18951.hp1 NA18953.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+10351G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86605140 | ||||||
| chr4:86605191
|
G | A | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+10402G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86605191 | ||||||
| chr4:86605336
|
G | C | 1 | a0003c0009t0001g0040 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-6+10547G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86605336 | ||||||
| chr4:86605377
|
A | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+10588A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86605377 | ||||||
| chr4:86605948
|
C | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+11159C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86605948 | ||||||
| chr4:86606124
|
GAATTA | G | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-6+11338_-6+11342d others(7): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86606124 | |||||
| chr4:86606711
|
T | C | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6+11922T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86606711 | ||||||
| chr4:86607462
|
T | C | 6 | a0003c0002t0002g0012a0003c0002t0002g0014a0003c0002t0002g0015others(3): Show | 6 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+12673T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86607462 | ||||||
| chr4:86607578
|
C | A | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+12789C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86607578 | ||||||
| chr4:86607613
|
C | T | 81 | a0001c0003t0002g0006a0001c0004t0002g0126a0002c0001t0002g0104others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.-6+12824C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86607613 | ||||||
| chr4:86607688
|
T | C | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+12899T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86607688 | ||||||
| chr4:86607857
|
C | T | 3 | a0004c0005t0005g0076a0004c0005t0005g0084a0004c0028t0005g0077 | 3 | HG00738.hp2 HG01099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-6+13068C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86607857 | ||||||
| chr4:86607860
|
C | T | 9 | a0001c0003t0002g0006a0003c0002t0002g0007a0003c0002t0002g0010others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-6+13071C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86607860 | ||||||
| chr4:86607925
|
A | G | 8 | a0001c0004t0001g0069a0001c0004t0001g0070a0001c0004t0001g0071others(5): Show | 8 | HG00609.hp1 HG01981.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6+13136A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86607925 | ||||||
| chr4:86607961
|
A | C | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+13172A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86607961 | ||||||
| chr4:86608089
|
G | A | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-6+13300G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86608089 | ||||||
| chr4:86608257
|
C | T | 196 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-6+13468C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86608257 | ||||||
| chr4:86608373
|
T | A | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+13584T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86608373 | ||||||
| chr4:86608377
|
T | C | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-6+13588T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86608377 | ||||||
| chr4:86608569
|
T | C | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+13780T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86608569 | ||||||
| chr4:86609190
|
C | A | 74 | a0001c0003t0002g0006a0001c0004t0002g0126a0002c0001t0002g0104others(71): Show | 74 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-6+14401C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86609190 | ||||||
| chr4:86609190
|
C | T | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-6+14401C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86609190 | ||||||
| chr4:86609288
|
T | C | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+14499T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86609288 | ||||||
| chr4:86609382
|
A | C | 4 | a0002c0001t0002g0158a0002c0001t0002g0159a0002c0001t0002g0160others(1): Show | 4 | HG00609.hp2 HG02056.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+14593A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86609382 | ||||||
| chr4:86609445
|
T | C | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+14656T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86609445 | ||||||
| chr4:86609548
|
G | C | 1 | a0011c0015t0001g0041 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-6+14759G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86609548 | ||||||
| chr4:86609990
|
T | C | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+15201T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86609990 | ||||||
| chr4:86610070
|
C | T | 4 | a0003c0002t0003g0193a0006c0010t0003g0194a0006c0010t0003g0195others(1): Show | 4 | HG02486.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+15281C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86610070 | ||||||
| chr4:86610128
|
C | T | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+15339C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86610128 | ||||||
| chr4:86610154
|
C | T | 1 | a0003c0002t0001g0189 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-6+15365C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86610154 | ||||||
| chr4:86610200
|
A | G | 91 | a0001c0003t0002g0006a0001c0004t0002g0126a0002c0001t0002g0104others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-6+15411A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86610200 | ||||||
| chr4:86610297
|
C | CT | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+15510dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86610297 | |||||
| chr4:86610512
|
G | A | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+15723G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86610512 | ||||||
| chr4:86610690
|
A | T | 4 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(1): Show | 4 | HG02486.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+15901A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86610690 | ||||||
| chr4:86610709
|
T | C | 1 | a0015c0021t0001g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-6+15920T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86610709 | ||||||
| chr4:86610811
|
C | T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6+16022C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86610811 | ||||||
| chr4:86611052
|
T | A | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+16263T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86611052 | ||||||
| chr4:86611089
|
C | A | 3 | a0002c0001t0002g0129a0002c0001t0002g0130a0002c0001t0002g0131 | 3 | HG00280.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-6+16300C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86611089 | ||||||
| chr4:86611549
|
T | C | 5 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(2): Show | 5 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+16760T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86611549 | ||||||
| chr4:86611670
|
G | C | 66 | a0001c0004t0002g0126a0002c0001t0002g0104a0002c0001t0002g0105others(63): Show | 66 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.-6+16881G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86611670 | ||||||
| chr4:86611679
|
A | C | 1 | a0001c0003t0001g0068 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-6+16890A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86611679 | ||||||
| chr4:86611798
|
A | G | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-6+17009A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86611798 | ||||||
| chr4:86611999
|
G | T | 196 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-6+17210G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86611999 | ||||||
| chr4:86612163
|
A | T | 1 | a0003c0002t0002g0017 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-6+17374A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86612163 | ||||||
| chr4:86612227
|
G | A | 1 | a0007c0007t0004g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-6+17438G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86612227 | ||||||
| chr4:86612706
|
A | C | 3 | a0008c0014t0003g0025a0008c0014t0003g0026a0022c0031t0003g0027 | 3 | HG02145.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-6+17917A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86612706 | ||||||
| chr4:86612709
|
C | T | 2 | a0001c0004t0001g0086a0001c0004t0007g0067 | 2 | NA19003.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-6+17920C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86612709 | ||||||
| chr4:86612810
|
G | C | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6+18021G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86612810 | ||||||
| chr4:86612900
|
G | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+18111G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86612900 | ||||||
| chr4:86612908
|
T | C | 197 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-6+18119T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86612908 | ||||||
| chr4:86613094
|
T | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6+18305T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86613094 | ||||||
| chr4:86613108
|
A | G | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+18319A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86613108 | ||||||
| chr4:86613418
|
G | A | 7 | a0003c0002t0002g0012a0003c0002t0002g0014a0003c0002t0002g0015others(4): Show | 7 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+18629G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86613418 | ||||||
| chr4:86613478
|
C | T | 1 | a0001c0004t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-6+18689C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86613478 | ||||||
| chr4:86613495
|
G | A | 1 | a0011c0015t0001g0041 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-6+18706G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86613495 | ||||||
| chr4:86613583
|
A | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+18794A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86613583 | ||||||
| chr4:86613623
|
G | A | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-6+18834G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86613623 | ||||||
| chr4:86613633
|
C | CA | 26 | a0001c0004t0002g0126a0002c0001t0002g0105a0002c0001t0002g0106others(23): Show | 26 | HG00423.hp1 HG01071.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.-6+18862dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86613633 | |||||
| chr4:86613633
|
C | CAAAAAAA others(5): Show |
1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-6+18851_-6+18862d others(14): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86613633 | |||||
| chr4:86613633
|
C | CAAAAAAA others(8): Show |
1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-6+18848_-6+18862d others(17): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86613633 | |||||
| chr4:86613633
|
C | CAAAAAAA others(9): Show |
1 | a0019c0024t0004g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-6+18847_-6+18862d others(18): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86613633 | |||||
| chr4:86613633
|
C | CAAAAAAA others(10): Show |
3 | a0003c0002t0002g0007a0004c0005t0004g0004a0004c0005t0004g0005 | 3 | HG00639.hp1 HG01123.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-6+18846_-6+18862d others(19): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86613633 | |||||
| chr4:86613633
|
C | CAAAAAAA others(11): Show |
4 | a0001c0003t0002g0006a0003c0002t0002g0016a0004c0005t0004g0001others(1): Show | 4 | HG01175.hp2 HG01192.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+18845_-6+18862d others(20): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86613633 | |||||
| chr4:86613633
|
C | CAAAAAAA others(12): Show |
2 | a0003c0002t0002g0015a0003c0002t0002g0017 | 2 | HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-6+18862_-6+18863i others(21): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86613633 | |||||
| chr4:86613633
|
C | CAAAAAAA others(13): Show |
2 | a0003c0002t0002g0014a0004c0005t0004g0002 | 2 | HG01346.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-6+18862_-6+18863i others(22): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86613633 | |||||
| chr4:86613633
|
C | CAAAAAAA others(15): Show |
1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6+18862_-6+18863i others(24): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86613633 | |||||
| chr4:86613633
|
CA | C | 13 | a0001c0003t0001g0039a0002c0001t0002g0156a0002c0001t0002g0157others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6+18862delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86613633 | |||||
| chr4:86613772
|
G | A | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+18983G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86613772 | ||||||
| chr4:86613841
|
G | C | 3 | a0007c0007t0004g0167a0007c0007t0005g0175a0007c0007t0005g0179 | 3 | HG02280.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-6+19052G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86613841 | ||||||
| chr4:86613970
|
A | G | 1 | a0001c0003t0001g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-6+19181A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86613970 | ||||||
| chr4:86614111
|
A | G | 1 | a0002c0001t0002g0127 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-6+19322A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86614111 | ||||||
| chr4:86614170
|
C | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+19381C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86614170 | ||||||
| chr4:86614687
|
A | G | 2 | a0003c0006t0003g0023a0003c0006t0003g0024 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-6+19898A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86614687 | ||||||
| chr4:86614950
|
A | C | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6+20161A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86614950 | ||||||
| chr4:86615077
|
T | C | 62 | a0001c0004t0002g0126a0002c0001t0002g0104a0002c0001t0002g0105others(59): Show | 62 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.-5-20175T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86615077 | ||||||
| chr4:86615110
|
C | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-20142C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86615110 | ||||||
| chr4:86615177
|
A | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-20075A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86615177 | ||||||
| chr4:86615362
|
C | G | 16 | a0001c0003t0002g0006a0003c0002t0002g0007a0003c0002t0002g0010others(13): Show | 16 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.-5-19890C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86615362 | ||||||
| chr4:86615524
|
T | C | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-5-19728T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86615524 | ||||||
| chr4:86615563
|
T | C | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-5-19689T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86615563 | ||||||
| chr4:86615632
|
A | G | 1 | a0002c0001t0002g0131 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-5-19620A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86615632 | ||||||
| chr4:86615959
|
G | T | 1 | a0001c0004t0001g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-5-19293G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86615959 | ||||||
| chr4:86616284
|
T | C | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-18968T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86616284 | ||||||
| chr4:86616365
|
C | T | 1 | a0001c0003t0001g0033 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-5-18887C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86616365 | ||||||
| chr4:86616409
|
G | A | 49 | a0001c0003t0001g0035a0001c0003t0001g0037a0001c0003t0001g0038others(46): Show | 49 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.-5-18843G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86616409 | ||||||
| chr4:86616517
|
G | C | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-5-18735G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86616517 | ||||||
| chr4:86616548
|
G | A | 4 | a0008c0014t0003g0025a0008c0014t0003g0026a0008c0032t0003g0028others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-18704G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86616548 | ||||||
| chr4:86616626
|
C | T | 1 | a0022c0031t0003g0027 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-5-18626C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86616626 | ||||||
| chr4:86616650
|
G | A | 196 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-5-18602G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86616650 | ||||||
| chr4:86616694
|
C | T | 5 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(2): Show | 5 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-18558C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86616694 | ||||||
| chr4:86616857
|
A | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-5-18395A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86616857 | ||||||
| chr4:86616947
|
G | C | 65 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(62): Show | 65 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-5-18305G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86616947 | ||||||
| chr4:86617023
|
TA | T | 90 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-5-18225delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86617023 | |||||
| chr4:86617263
|
A | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-17989A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86617263 | ||||||
| chr4:86617285
|
A | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-17967A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86617285 | ||||||
| chr4:86617296
|
TA | T | 4 | a0001c0003t0001g0088a0001c0003t0001g0089a0001c0003t0001g0094others(1): Show | 4 | HG02135.hp1 NA18974.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-17955delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86617296 | ||||||
| chr4:86617532
|
A | G | 82 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-5-17720A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86617532 | ||||||
| chr4:86617962
|
G | T | 1 | a0001c0003t0001g0038 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-5-17290G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86617962 | ||||||
| chr4:86617987
|
T | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-5-17265T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86617987 | ||||||
| chr4:86618170
|
T | G | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-5-17082T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618170 | ||||||
| chr4:86618187
|
G | A | 2 | a0001c0004t0001g0069a0001c0004t0001g0070 | 2 | NA18944.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-5-17065G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618187 | ||||||
| chr4:86618266
|
G | T | 1 | a0001c0003t0001g0057 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-5-16986G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618266 | ||||||
| chr4:86618330
|
T | C | 1 | a0003c0002t0005g0169 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-5-16922T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618330 | ||||||
| chr4:86618339
|
A | G | 1 | a0004c0005t0004g0002 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-5-16913A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618339 | ||||||
| chr4:86618357
|
G | A | 65 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(62): Show | 65 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-5-16895G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618357 | ||||||
| chr4:86618359
|
G | A | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-16893G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618359 | ||||||
| chr4:86618407
|
T | C | 65 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(62): Show | 65 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-5-16845T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618407 | ||||||
| chr4:86618408
|
G | A | 65 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(62): Show | 65 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-5-16844G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618408 | ||||||
| chr4:86618459
|
T | G | 1 | a0001c0003t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-5-16793T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618459 | ||||||
| chr4:86618485
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-5-16767G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618485 | ||||||
| chr4:86618519
|
T | G | 1 | a0003c0002t0002g0017 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-5-16733T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618519 | ||||||
| chr4:86618752
|
A | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-16500A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618752 | ||||||
| chr4:86618864
|
C | T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-5-16388C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618864 | ||||||
| chr4:86618865
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-5-16387G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618865 | ||||||
| chr4:86618903
|
A | G | 4 | a0008c0014t0003g0025a0008c0014t0003g0026a0008c0032t0003g0028others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-16349A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618903 | ||||||
| chr4:86618970
|
A | T | 65 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(62): Show | 65 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-5-16282A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618970 | ||||||
| chr4:86618988
|
T | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-16264T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86618988 | ||||||
| chr4:86619134
|
C | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-5-16118C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86619134 | ||||||
| chr4:86619764
|
CT | C | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-15477delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86619764 | |||||
| chr4:86619775
|
T | C | 4 | a0001c0003t0001g0059a0001c0003t0001g0060a0001c0003t0001g0061others(1): Show | 4 | HG01175.hp1 HG02717.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-15477T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86619775 | ||||||
| chr4:86619849
|
C | A | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-15403C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86619849 | ||||||
| chr4:86620099
|
A | G | 92 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-5-15153A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86620099 | ||||||
| chr4:86620126
|
A | G | 1 | a0001c0003t0001g0093 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-5-15126A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86620126 | ||||||
| chr4:86620239
|
C | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-5-15013C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86620239 | ||||||
| chr4:86620287
|
T | C | 1 | a0001c0004t0001g0181 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-5-14965T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86620287 | ||||||
| chr4:86620996
|
T | C | 82 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-5-14256T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86620996 | ||||||
| chr4:86621028
|
T | A | 1 | a0001c0003t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-5-14224T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86621028 | ||||||
| chr4:86621146
|
C | CAT | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-14106_-5-14105i others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86621146 | ||||||
| chr4:86621153
|
A | T | 1 | a0001c0004t0001g0070 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-5-14099A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86621153 | ||||||
| chr4:86621154
|
T | G | 1 | a0001c0004t0001g0070 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-5-14098T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86621154 | ||||||
| chr4:86621155
|
C | T | 1 | a0001c0004t0001g0070 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-5-14097C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86621155 | ||||||
| chr4:86621784
|
G | A | 2 | a0007c0007t0005g0175a0007c0007t0005g0179 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-5-13468G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86621784 | ||||||
| chr4:86622228
|
T | C | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-5-13024T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86622228 | ||||||
| chr4:86622298
|
A | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-12954A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86622298 | ||||||
| chr4:86622424
|
G | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-5-12828G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86622424 | ||||||
| chr4:86622694
|
T | C | 73 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(70): Show | 73 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-5-12558T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86622694 | ||||||
| chr4:86622839
|
A | G | 1 | a0019c0024t0004g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-5-12413A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86622839 | ||||||
| chr4:86623125
|
G | A | 3 | a0002c0001t0002g0134a0002c0001t0002g0135a0002c0001t0002g0136 | 3 | NA18944.hp2 NA18948.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-5-12127G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86623125 | ||||||
| chr4:86623331
|
A | G | 2 | a0002c0001t0002g0154a0002c0001t0002g0155 | 2 | HG00140.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-5-11921A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86623331 | ||||||
| chr4:86623576
|
C | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-11676C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86623576 | ||||||
| chr4:86623766
|
G | T | 2 | a0001c0004t0001g0055a0001c0004t0001g0056 | 2 | HG00438.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-5-11486G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86623766 | ||||||
| chr4:86623768
|
A | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-11484A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86623768 | ||||||
| chr4:86624055
|
G | A | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-11197G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86624055 | ||||||
| chr4:86624072
|
G | A | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-11180G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86624072 | ||||||
| chr4:86624204
|
A | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-11048A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86624204 | ||||||
| chr4:86624210
|
C | A | 1 | a0003c0002t0001g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-5-11042C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86624210 | ||||||
| chr4:86624425
|
T | C | 1 | a0002c0001t0002g0105 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-5-10827T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86624425 | ||||||
| chr4:86624453
|
G | A | 1 | a0006c0010t0003g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-5-10799G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86624453 | ||||||
| chr4:86624953
|
C | T | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-5-10299C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86624953 | ||||||
| chr4:86625293
|
T | G | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-5-9959T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86625293 | ||||||
| chr4:86625306
|
A | G | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-5-9946A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86625306 | ||||||
| chr4:86625466
|
C | G | 64 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(61): Show | 64 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-5-9786C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86625466 | ||||||
| chr4:86625577
|
T | C | 64 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(61): Show | 64 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-5-9675T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86625577 | ||||||
| chr4:86625753
|
C | T | 2 | a0001c0004t0001g0069a0001c0004t0001g0070 | 2 | NA18944.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-5-9499C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86625753 | ||||||
| chr4:86625757
|
C | A | 1 | a0003c0002t0001g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-5-9495C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86625757 | ||||||
| chr4:86625875
|
A | T | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-9377A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86625875 | ||||||
| chr4:86626062
|
G | T | 1 | a0002c0001t0002g0153 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-9190G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86626062 | ||||||
| chr4:86626270
|
G | T | 1 | a0005c0008t0002g0152 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-5-8982G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86626270 | ||||||
| chr4:86626561
|
T | C | 1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5-8691T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86626561 | ||||||
| chr4:86626603
|
A | G | 1 | a0003c0002t0001g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-5-8649A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86626603 | ||||||
| chr4:86626725
|
A | G | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-5-8527A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86626725 | ||||||
| chr4:86626795
|
G | A | 1 | a0001c0003t0001g0093 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-5-8457G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86626795 | ||||||
| chr4:86627298
|
A | G | 1 | a0002c0001t0002g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-5-7954A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86627298 | ||||||
| chr4:86627314
|
T | C | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-5-7938T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86627314 | ||||||
| chr4:86627486
|
C | A | 4 | a0008c0014t0003g0025a0008c0014t0003g0026a0008c0032t0003g0028others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-7766C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86627486 | ||||||
| chr4:86627508
|
G | T | 3 | a0001c0003t0001g0092a0003c0002t0002g0010a0020c0020t0001g0054 | 3 | HG03098.hp1 HG04228.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-5-7744G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86627508 | ||||||
| chr4:86627508
|
GT | G | 72 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-5-7733delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86627508 | |||||
| chr4:86627515
|
T | C | 72 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-5-7737T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86627515 | ||||||
| chr4:86627804
|
A | G | 1 | a0003c0002t0001g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-5-7448A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86627804 | ||||||
| chr4:86627819
|
C | T | 1 | a0003c0002t0001g0178 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-5-7433C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86627819 | ||||||
| chr4:86627943
|
T | C | 64 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(61): Show | 64 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-5-7309T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86627943 | ||||||
| chr4:86628014
|
A | G | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-5-7238A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86628014 | ||||||
| chr4:86628401
|
T | C | 1 | a0007c0007t0004g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-5-6851T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86628401 | ||||||
| chr4:86628433
|
G | C | 4 | a0003c0002t0001g0168a0003c0002t0001g0171a0003c0002t0001g0172others(1): Show | 4 | HG01243.hp2 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-6819G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86628433 | ||||||
| chr4:86628441
|
T | C | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-5-6811T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86628441 | ||||||
| chr4:86628460
|
T | C | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-6792T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86628460 | ||||||
| chr4:86628490
|
A | ATT | 17 | a0001c0003t0002g0006a0002c0001t0002g0129a0002c0001t0002g0133others(14): Show | 17 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.-5-6752_-5-6751dup others(2): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86628490 | |||||
| chr4:86628490
|
A | ATTT | 55 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(52): Show | 55 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.-5-6753_-5-6751dup others(3): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86628490 | |||||
| chr4:86628501
|
T | A | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-6751T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86628501 | ||||||
| chr4:86628501
|
T | TTA | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-6751_-5-6750ins others(2): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86628501 | ||||||
| chr4:86628502
|
A | T | 8 | a0002c0001t0002g0133a0002c0001t0002g0134a0002c0001t0002g0135others(5): Show | 8 | HG02135.hp2 NA18612.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-6750A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86628502 | ||||||
| chr4:86628503
|
A | AT | 86 | a0001c0003t0001g0035a0001c0003t0001g0037a0001c0003t0001g0038others(83): Show | 86 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.-5-6738dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86628503 | |||||
| chr4:86628503
|
A | T | 11 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(8): Show | 11 | HG01891.hp1 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-5-6749A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86628503 | ||||||
| chr4:86628504
|
T | A | 8 | a0002c0001t0002g0133a0002c0001t0002g0134a0002c0001t0002g0135others(5): Show | 8 | HG02135.hp2 NA18612.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-6748T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86628504 | ||||||
| chr4:86628646
|
TC | T | 72 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-5-6600delC | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86628646 | |||||
| chr4:86628648
|
C | A | 64 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(61): Show | 64 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-5-6604C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86628648 | ||||||
| chr4:86628659
|
G | A | 1 | a0002c0001t0002g0140 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-5-6593G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86628659 | ||||||
| chr4:86628775
|
A | G | 1 | a0001c0004t0001g0181 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-5-6477A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86628775 | ||||||
| chr4:86629151
|
C | T | 40 | a0001c0003t0002g0006a0001c0004t0001g0032a0001c0004t0001g0048others(37): Show | 40 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.-5-6101C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86629151 | ||||||
| chr4:86629196
|
C | T | 1 | a0002c0001t0002g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-5-6056C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86629196 | ||||||
| chr4:86629482
|
A | G | 1 | a0002c0001t0002g0160 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-5-5770A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86629482 | ||||||
| chr4:86629522
|
A | C | 60 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.-5-5730A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86629522 | ||||||
| chr4:86629648
|
C | A | 72 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-5-5604C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86629648 | ||||||
| chr4:86629651
|
A | G | 72 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-5-5601A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86629651 | ||||||
| chr4:86629682
|
G | T | 72 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-5-5570G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86629682 | ||||||
| chr4:86629784
|
G | T | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-5468G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86629784 | ||||||
| chr4:86629930
|
T | A | 3 | a0002c0001t0002g0141a0002c0001t0002g0142a0018c0023t0002g0143 | 3 | HG00642.hp2 HG01361.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-5-5322T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86629930 | ||||||
| chr4:86629972
|
G | T | 5 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(2): Show | 5 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-5280G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86629972 | ||||||
| chr4:86630146
|
T | C | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-5-5106T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86630146 | ||||||
| chr4:86630172
|
G | A | 72 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-5-5080G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86630172 | ||||||
| chr4:86630318
|
T | C | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-4934T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86630318 | ||||||
| chr4:86630329
|
C | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-5-4923C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86630329 | ||||||
| chr4:86630453
|
A | G | 1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5-4799A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86630453 | ||||||
| chr4:86630508
|
T | G | 1 | a0003c0002t0001g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-5-4744T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86630508 | ||||||
| chr4:86630609
|
G | GT | 3 | a0004c0005t0005g0076a0004c0005t0005g0084a0004c0028t0005g0077 | 3 | HG00738.hp2 HG01099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-5-4637dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86630609 | |||||
| chr4:86630687
|
C | T | 174 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-5-4565C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86630687 | ||||||
| chr4:86631172
|
C | T | 1 | a0002c0001t0002g0125 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-5-4080C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86631172 | ||||||
| chr4:86631219
|
A | T | 1 | a0001c0004t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-5-4033A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86631219 | ||||||
| chr4:86631280
|
T | C | 5 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(2): Show | 5 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-3972T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86631280 | ||||||
| chr4:86631480
|
A | G | 4 | a0002c0001t0002g0158a0002c0001t0002g0159a0002c0001t0002g0160others(1): Show | 4 | HG00609.hp2 HG02056.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-3772A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86631480 | ||||||
| chr4:86631635
|
C | T | 1 | a0019c0024t0004g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-5-3617C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86631635 | ||||||
| chr4:86631714
|
G | A | 1 | a0002c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-5-3538G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86631714 | ||||||
| chr4:86631719
|
C | T | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-3533C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86631719 | ||||||
| chr4:86631750
|
C | T | 72 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-5-3502C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86631750 | ||||||
| chr4:86631751
|
A | G | 8 | a0001c0003t0002g0006a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-3501A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86631751 | ||||||
| chr4:86631801
|
A | T | 1 | a0002c0001t0002g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-5-3451A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86631801 | ||||||
| chr4:86632052
|
A | ATCCTTCC others(9): Show |
79 | a0001c0003t0002g0006a0002c0001t0002g0104a0002c0001t0002g0105others(76): Show | 79 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-5-3191_-5-3190ins others(16): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr4 | 86632052 | |||||
| chr4:86632052
|
A | T | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-5-3200A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86632052 | ||||||
| chr4:86632571
|
C | T | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-2681C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86632571 | ||||||
| chr4:86632649
|
C | T | 3 | a0001c0003t0001g0044a0001c0003t0001g0057a0015c0021t0001g0042 | 3 | HG01081.hp2 HG01361.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.-5-2603C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86632649 | ||||||
| chr4:86632727
|
A | G | 1 | a0007c0007t0004g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-5-2525A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86632727 | ||||||
| chr4:86632770
|
G | A | 3 | a0001c0004t0002g0046a0001c0004t0002g0047a0016c0019t0002g0045 | 3 | HG01517.hp2 HG01978.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-5-2482G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86632770 | ||||||
| chr4:86632868
|
G | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-5-2384G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86632868 | ||||||
| chr4:86632933
|
T | A | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-5-2319T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86632933 | ||||||
| chr4:86633035
|
G | T | 3 | a0001c0004t0002g0046a0001c0004t0002g0047a0016c0019t0002g0045 | 3 | HG01517.hp2 HG01978.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-5-2217G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86633035 | ||||||
| chr4:86633071
|
G | A | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-2181G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86633071 | ||||||
| chr4:86633180
|
A | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5-2072A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86633180 | ||||||
| chr4:86633252
|
C | A | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-5-2000C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86633252 | ||||||
| chr4:86633400
|
C | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5-1852C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86633400 | ||||||
| chr4:86633945
|
T | C | 2 | a0001c0003t0001g0062a0001c0003t0002g0006 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-5-1307T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86633945 | ||||||
| chr4:86634022
|
A | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-5-1230A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86634022 | ||||||
| chr4:86634414
|
C | T | 1 | a0004c0028t0005g0077 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-5-838C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86634414 | ||||||
| chr4:86634485
|
C | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5-767C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86634485 | ||||||
| chr4:86634570
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-5-682G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86634570 | ||||||
| chr4:86634594
|
C | G | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-5-658C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86634594 | ||||||
| chr4:86634760
|
G | A | 1 | a0001c0003t0001g0094 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-5-492G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86634760 | ||||||
| chr4:86634761
|
G | A | 1 | a0002c0001t0002g0131 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-5-491G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86634761 | ||||||
| chr4:86634878
|
A | T | 1 | a0003c0002t0001g0180 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-5-374A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86634878 | ||||||
| chr4:86635100
|
G | A | 14 | a0003c0002t0002g0007a0003c0002t0002g0012a0003c0002t0002g0014others(11): Show | 14 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.-5-152G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 1/47 | chr4 | 86635100 | ||||||
| chr4:86635395
|
T | C | 1 | a0002c0001t0002g0106 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.115+24T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86635395 | ||||||
| chr4:86635505
|
C | T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115+134C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86635505 | ||||||
| chr4:86635616
|
G | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+245G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86635616 | ||||||
| chr4:86635693
|
G | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+322G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86635693 | ||||||
| chr4:86635758
|
G | A | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+387G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86635758 | ||||||
| chr4:86635785
|
G | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+414G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86635785 | ||||||
| chr4:86636059
|
G | A | 3 | a0003c0002t0001g0183a0003c0002t0001g0197a0003c0002t0002g0184 | 3 | HG01081.hp1 HG01496.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.115+688G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86636059 | ||||||
| chr4:86636390
|
G | GT | 60 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.115+1019_115+1020i others(3): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86636390 | ||||||
| chr4:86636391
|
C | G | 60 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.115+1020C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86636391 | ||||||
| chr4:86636393
|
ATT | A | 60 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.115+1023_115+1024d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86636393 | ||||||
| chr4:86636398
|
T | C | 1 | a0002c0001t0002g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.115+1027T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86636398 | ||||||
| chr4:86636446
|
G | A | 1 | a0001c0004t0001g0048 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.115+1075G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86636446 | ||||||
| chr4:86636662
|
G | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+1291G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86636662 | ||||||
| chr4:86636665
|
C | T | 2 | a0002c0001t0002g0142a0018c0023t0002g0143 | 2 | HG00642.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.115+1294C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86636665 | ||||||
| chr4:86636666
|
A | G | 2 | a0002c0001t0002g0142a0018c0023t0002g0143 | 2 | HG00642.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.115+1295A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86636666 | ||||||
| chr4:86636973
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115+1602G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86636973 | ||||||
| chr4:86636976
|
A | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+1605A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86636976 | ||||||
| chr4:86637132
|
A | G | 88 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(85): Show | 88 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.115+1761A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86637132 | ||||||
| chr4:86637243
|
C | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115+1872C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86637243 | ||||||
| chr4:86637528
|
C | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+2157C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86637528 | ||||||
| chr4:86637572
|
CAA | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+2205_115+2206d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86637572 | |||||
| chr4:86637720
|
A | G | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.115+2349A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86637720 | ||||||
| chr4:86637791
|
A | C | 4 | a0001c0004t0001g0087a0002c0001t0002g0134a0002c0001t0002g0135others(1): Show | 4 | HG01106.hp2 NA18944.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2420A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86637791 | ||||||
| chr4:86637846
|
A | G | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.115+2475A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86637846 | ||||||
| chr4:86637866
|
A | G | 2 | a0003c0002t0002g0007a0019c0024t0004g0008 | 2 | HG00639.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.115+2495A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86637866 | ||||||
| chr4:86637874
|
A | C | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.115+2503A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86637874 | ||||||
| chr4:86637913
|
T | C | 1 | a0002c0001t0002g0140 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.115+2542T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86637913 | ||||||
| chr4:86637935
|
C | G | 5 | a0001c0003t0001g0079a0001c0003t0001g0080a0001c0003t0001g0081others(2): Show | 5 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+2564C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86637935 | ||||||
| chr4:86637935
|
C | T | 10 | a0001c0003t0001g0065a0001c0004t0001g0051a0001c0004t0001g0052others(7): Show | 10 | HG00438.hp1 HG02083.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.115+2564C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86637935 | ||||||
| chr4:86637936
|
G | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+2565G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86637936 | ||||||
| chr4:86638039
|
C | T | 1 | a0001c0004t0001g0032 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.115+2668C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638039 | ||||||
| chr4:86638062
|
T | C | 1 | a0001c0003t0001g0088 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.115+2691T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638062 | ||||||
| chr4:86638102
|
T | C | 1 | a0004c0005t0004g0003 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.115+2731T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638102 | ||||||
| chr4:86638123
|
A | G | 8 | a0001c0003t0001g0066a0003c0002t0002g0007a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+2752A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638123 | ||||||
| chr4:86638125
|
C | T | 1 | a0001c0003t0001g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.115+2754C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638125 | ||||||
| chr4:86638225
|
G | A | 1 | a0002c0001t0002g0107 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.115+2854G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638225 | ||||||
| chr4:86638268
|
C | G | 3 | a0007c0007t0004g0167a0007c0007t0005g0175a0007c0007t0005g0179 | 3 | HG02280.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.115+2897C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638268 | ||||||
| chr4:86638356
|
A | C | 1 | a0002c0011t0002g0124 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.115+2985A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638356 | ||||||
| chr4:86638580
|
A | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+3209A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638580 | ||||||
| chr4:86638581
|
C | T | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.115+3210C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638581 | ||||||
| chr4:86638738
|
C | T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115+3367C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638738 | ||||||
| chr4:86638815
|
C | A | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.115+3444C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638815 | ||||||
| chr4:86638846
|
A | C | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.115+3475A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638846 | ||||||
| chr4:86638941
|
G | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.115+3570G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86638941 | ||||||
| chr4:86639022
|
G | C | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.115+3651G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639022 | ||||||
| chr4:86639049
|
T | G | 8 | a0003c0002t0003g0193a0006c0010t0003g0194a0006c0010t0003g0195others(5): Show | 8 | HG02280.hp1 HG02486.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+3678T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639049 | ||||||
| chr4:86639052
|
C | T | 8 | a0003c0002t0003g0193a0006c0010t0003g0194a0006c0010t0003g0195others(5): Show | 8 | HG02280.hp1 HG02486.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+3681C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639052 | ||||||
| chr4:86639187
|
G | C | 3 | a0007c0007t0004g0132a0007c0007t0005g0175a0007c0007t0005g0179 | 3 | HG02280.hp1 HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.115+3816G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639187 | ||||||
| chr4:86639204
|
C | T | 16 | a0003c0002t0002g0007a0003c0002t0002g0010a0003c0002t0002g0012others(13): Show | 16 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.115+3833C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639204 | ||||||
| chr4:86639208
|
A | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+3837A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639208 | ||||||
| chr4:86639229
|
G | A | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.115+3858G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639229 | ||||||
| chr4:86639263
|
A | G | 2 | a0003c0002t0009g0188a0012c0016t0006g0198 | 2 | HG01981.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.115+3892A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639263 | ||||||
| chr4:86639378
|
A | T | 2 | a0001c0003t0001g0062a0001c0003t0002g0006 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.115+4007A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639378 | ||||||
| chr4:86639451
|
G | A | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.115+4080G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639451 | ||||||
| chr4:86639498
|
TA | T | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+4134delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86639498 | |||||
| chr4:86639542
|
A | T | 1 | a0001c0017t0001g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.115+4171A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639542 | ||||||
| chr4:86639554
|
C | T | 1 | a0001c0004t0001g0032 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.115+4183C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639554 | ||||||
| chr4:86639569
|
A | G | 1 | a0003c0002t0001g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.115+4198A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639569 | ||||||
| chr4:86639606
|
T | A | 16 | a0003c0002t0002g0007a0003c0002t0002g0010a0003c0002t0002g0012others(13): Show | 16 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.115+4235T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86639606 | ||||||
| chr4:86639826
|
T | TA | 9 | a0003c0002t0001g0168a0003c0002t0002g0007a0004c0005t0004g0001others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+4466dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86639826 | |||||
| chr4:86640152
|
A | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115+4781A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86640152 | ||||||
| chr4:86640380
|
T | C | 1 | a0003c0002t0001g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.115+5009T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86640380 | ||||||
| chr4:86640517
|
G | A | 14 | a0003c0002t0002g0007a0003c0002t0002g0012a0003c0002t0002g0014others(11): Show | 14 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.115+5146G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86640517 | ||||||
| chr4:86640583
|
C | T | 3 | a0003c0002t0001g0099a0003c0002t0001g0100a0003c0002t0001g0101 | 3 | HG02451.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.115+5212C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86640583 | ||||||
| chr4:86640835
|
T | G | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.115+5464T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86640835 | ||||||
| chr4:86641226
|
A | C | 14 | a0003c0002t0002g0007a0003c0002t0002g0012a0003c0002t0002g0014others(11): Show | 14 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.115+5855A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86641226 | ||||||
| chr4:86641416
|
A | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+6045A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86641416 | ||||||
| chr4:86641745
|
G | A | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.115+6374G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86641745 | ||||||
| chr4:86641964
|
A | C | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+6593A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86641964 | ||||||
| chr4:86642326
|
G | C | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.115+6955G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86642326 | ||||||
| chr4:86642446
|
C | CTTT | 5 | a0003c0002t0002g0007a0004c0005t0004g0002a0004c0005t0004g0003others(2): Show | 5 | HG00639.hp1 HG01123.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+7077_115+7078i others(5): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86642446 | |||||
| chr4:86642447
|
TTC | T | 10 | a0001c0003t0001g0039a0001c0004t0001g0075a0001c0004t0002g0126others(7): Show | 10 | HG01099.hp2 HG01243.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.115+7078_115+7079d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86642447 | |||||
| chr4:86642448
|
TC | T | 159 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(156): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.115+7078delC | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86642448 | ||||||
| chr4:86642449
|
C | CTT | 6 | a0003c0002t0002g0012a0003c0002t0002g0014a0003c0002t0002g0015others(3): Show | 6 | HG02486.hp2 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.115+7098_115+7099d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86642449 | |||||
| chr4:86642449
|
C | T | 20 | a0001c0003t0001g0062a0001c0003t0001g0064a0001c0004t0001g0050others(17): Show | 20 | HG00639.hp1 HG00642.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.115+7078C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86642449 | ||||||
| chr4:86642480
|
T | G | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.115+7109T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86642480 | ||||||
| chr4:86642563
|
G | A | 5 | a0003c0002t0003g0193a0006c0010t0003g0194a0006c0010t0003g0195others(2): Show | 5 | HG02486.hp1 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.115+7192G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86642563 | ||||||
| chr4:86642732
|
G | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+7361G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86642732 | ||||||
| chr4:86642747
|
G | A | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.115+7376G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86642747 | ||||||
| chr4:86642762
|
C | T | 1 | a0007c0007t0005g0175 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.115+7391C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86642762 | ||||||
| chr4:86642812
|
A | G | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.115+7441A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86642812 | ||||||
| chr4:86642901
|
T | C | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.115+7530T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86642901 | ||||||
| chr4:86643343
|
T | C | 1 | a0002c0001t0002g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.115+7972T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86643343 | ||||||
| chr4:86643763
|
A | G | 4 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(1): Show | 4 | HG02486.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+8392A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86643763 | ||||||
| chr4:86643799
|
G | T | 4 | a0002c0001t0002g0149a0005c0008t0002g0128a0005c0008t0002g0150others(1): Show | 4 | NA18994.hp1 NA19007.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+8428G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86643799 | ||||||
| chr4:86644028
|
G | T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115+8657G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86644028 | ||||||
| chr4:86644219
|
C | T | 1 | a0001c0003t0001g0038 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.115+8848C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86644219 | ||||||
| chr4:86644420
|
A | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+9049A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86644420 | ||||||
| chr4:86644647
|
A | G | 1 | a0001c0004t0001g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.115+9276A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86644647 | ||||||
| chr4:86644786
|
G | T | 1 | a0003c0002t0001g0187 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.115+9415G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86644786 | ||||||
| chr4:86644874
|
A | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+9503A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86644874 | ||||||
| chr4:86644908
|
A | T | 1 | a0002c0001t0002g0157 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.115+9537A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86644908 | ||||||
| chr4:86645070
|
G | A | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+9699G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86645070 | ||||||
| chr4:86645097
|
T | G | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.115+9726T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86645097 | ||||||
| chr4:86645143
|
T | A | 1 | a0002c0001t0002g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.115+9772T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86645143 | ||||||
| chr4:86645184
|
C | T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115+9813C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86645184 | ||||||
| chr4:86645272
|
A | C | 1 | a0008c0032t0003g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.115+9901A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86645272 | ||||||
| chr4:86645966
|
A | T | 1 | a0001c0003t0001g0093 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.115+10595A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86645966 | ||||||
| chr4:86645991
|
A | G | 1 | a0002c0001t0002g0136 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.115+10620A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86645991 | ||||||
| chr4:86646102
|
TA | T | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+10740delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86646102 | |||||
| chr4:86646290
|
A | AT | 6 | a0001c0003t0002g0006a0001c0004t0001g0056a0001c0004t0001g0086others(3): Show | 6 | HG00438.hp1 HG02145.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.115+10943dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86646290 | |||||
| chr4:86646290
|
AT | A | 24 | a0001c0003t0001g0035a0001c0003t0001g0038a0001c0004t0001g0071others(21): Show | 24 | HG00639.hp1 HG01074.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.115+10943delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86646290 | |||||
| chr4:86646315
|
A | T | 1 | a0006c0010t0003g0196 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.115+10944A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86646315 | ||||||
| chr4:86646547
|
C | T | 1 | a0003c0009t0001g0040 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.115+11176C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86646547 | ||||||
| chr4:86646869
|
C | T | 1 | a0003c0006t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115+11498C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86646869 | ||||||
| chr4:86646875
|
A | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+11504A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86646875 | ||||||
| chr4:86647434
|
T | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+12063T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86647434 | ||||||
| chr4:86647491
|
G | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+12120G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86647491 | ||||||
| chr4:86647668
|
T | G | 1 | a0007c0007t0004g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115+12297T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86647668 | ||||||
| chr4:86647864
|
C | T | 2 | a0003c0002t0002g0010a0012c0016t0006g0198 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.115+12493C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86647864 | ||||||
| chr4:86647869
|
C | T | 3 | a0008c0014t0003g0025a0008c0014t0003g0026a0022c0031t0003g0027 | 3 | HG02145.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.115+12498C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86647869 | ||||||
| chr4:86648104
|
T | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+12733T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86648104 | ||||||
| chr4:86648299
|
C | T | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.115+12928C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86648299 | ||||||
| chr4:86648366
|
T | C | 1 | a0008c0032t0003g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.115+12995T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86648366 | ||||||
| chr4:86648421
|
A | G | 1 | a0003c0002t0001g0180 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.115+13050A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86648421 | ||||||
| chr4:86648421
|
A | T | 60 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.115+13050A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86648421 | ||||||
| chr4:86648883
|
C | T | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+13512C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86648883 | ||||||
| chr4:86649023
|
C | T | 1 | a0001c0003t0001g0063 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.115+13652C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86649023 | ||||||
| chr4:86649056
|
G | A | 60 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.115+13685G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86649056 | ||||||
| chr4:86649105
|
C | A | 1 | a0003c0002t0001g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.115+13734C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86649105 | ||||||
| chr4:86649305
|
G | A | 92 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.115+13934G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86649305 | ||||||
| chr4:86649609
|
A | G | 65 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(62): Show | 65 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.115+14238A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86649609 | ||||||
| chr4:86649676
|
G | T | 2 | a0002c0001t0002g0127a0002c0001t0002g0165 | 2 | NA18984.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.115+14305G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86649676 | ||||||
| chr4:86649679
|
C | G | 2 | a0002c0001t0002g0127a0002c0001t0002g0165 | 2 | NA18984.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.115+14308C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86649679 | ||||||
| chr4:86649949
|
T | G | 2 | a0001c0003t0001g0090a0001c0003t0001g0093 | 2 | HG01074.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.115+14578T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86649949 | ||||||
| chr4:86650029
|
C | T | 140 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(137): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.115+14658C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86650029 | ||||||
| chr4:86650043
|
T | C | 3 | a0003c0002t0001g0096a0003c0002t0001g0098a0003c0002t0001g0103 | 3 | HG02145.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.115+14672T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86650043 | ||||||
| chr4:86650123
|
A | C | 1 | a0003c0009t0001g0102 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.115+14752A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86650123 | ||||||
| chr4:86650168
|
G | T | 1 | a0001c0004t0001g0032 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.115+14797G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86650168 | ||||||
| chr4:86650363
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115+14992G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86650363 | ||||||
| chr4:86650436
|
C | T | 1 | a0002c0001t0002g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.115+15065C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86650436 | ||||||
| chr4:86650437
|
G | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+15066G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86650437 | ||||||
| chr4:86650701
|
T | C | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+15330T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86650701 | ||||||
| chr4:86650852
|
A | G | 3 | a0004c0005t0005g0076a0004c0005t0005g0084a0004c0028t0005g0077 | 3 | HG00738.hp2 HG01099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.115+15481A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86650852 | ||||||
| chr4:86650854
|
A | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+15483A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86650854 | ||||||
| chr4:86651046
|
G | A | 71 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(68): Show | 71 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.115+15675G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86651046 | ||||||
| chr4:86651071
|
T | C | 1 | a0003c0009t0002g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.115+15700T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86651071 | ||||||
| chr4:86651175
|
A | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115+15804A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86651175 | ||||||
| chr4:86651429
|
CCCTT | C | 3 | a0008c0014t0003g0025a0008c0014t0003g0026a0022c0031t0003g0027 | 3 | HG02145.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.115+16078_115+1608 others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86651429 | |||||
| chr4:86651674
|
A | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+16303A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86651674 | ||||||
| chr4:86651825
|
T | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+16454T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86651825 | ||||||
| chr4:86652194
|
T | TCTA | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+16824_115+1682 others(7): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86652194 | |||||
| chr4:86652354
|
G | C | 1 | a0006c0010t0003g0196 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.115+16983G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86652354 | ||||||
| chr4:86652481
|
G | A | 2 | a0003c0002t0001g0171a0003c0002t0001g0172 | 2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.115+17110G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86652481 | ||||||
| chr4:86652587
|
C | T | 2 | a0002c0001t0002g0142a0018c0023t0002g0143 | 2 | HG00642.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.115+17216C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86652587 | ||||||
| chr4:86652646
|
T | C | 3 | a0001c0004t0001g0181a0003c0002t0001g0091a0003c0002t0001g0190 | 3 | HG02273.hp1 NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.115+17275T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86652646 | ||||||
| chr4:86652650
|
T | C | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+17279T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86652650 | ||||||
| chr4:86653097
|
A | C | 2 | a0009c0012t0001g0185a0009c0012t0001g0191 | 2 | HG00438.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.115+17726A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86653097 | ||||||
| chr4:86653143
|
T | G | 1 | a0001c0017t0001g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.115+17772T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86653143 | ||||||
| chr4:86653299
|
C | T | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+17928C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86653299 | ||||||
| chr4:86653421
|
T | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+18050T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86653421 | ||||||
| chr4:86653486
|
G | A | 4 | a0008c0014t0003g0025a0008c0014t0003g0026a0008c0032t0003g0028others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+18115G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86653486 | ||||||
| chr4:86653489
|
T | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+18118T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86653489 | ||||||
| chr4:86653495
|
C | CT | 15 | a0001c0004t0001g0087a0002c0001t0002g0158a0002c0001t0002g0159others(12): Show | 15 | HG00609.hp2 HG01106.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.115+18138dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86653495 | |||||
| chr4:86653495
|
C | CTTTTT | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+18134_115+1813 others(9): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86653495 | |||||
| chr4:86653522
|
A | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+18151A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86653522 | ||||||
| chr4:86653633
|
A | G | 4 | a0003c0002t0001g0168a0003c0002t0001g0171a0003c0002t0001g0172others(1): Show | 4 | HG01243.hp2 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+18262A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86653633 | ||||||
| chr4:86653668
|
A | G | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.115+18297A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86653668 | ||||||
| chr4:86653719
|
G | T | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+18348G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86653719 | ||||||
| chr4:86653894
|
A | T | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-18471A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86653894 | ||||||
| chr4:86653949
|
A | G | 24 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0058others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.116-18416A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86653949 | ||||||
| chr4:86654022
|
G | A | 1 | a0001c0027t0001g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.116-18343G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86654022 | ||||||
| chr4:86654154
|
C | T | 1 | a0003c0002t0001g0180 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.116-18211C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86654154 | ||||||
| chr4:86654206
|
A | C | 3 | a0003c0002t0001g0099a0003c0002t0001g0100a0003c0002t0001g0101 | 3 | HG02451.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.116-18159A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86654206 | ||||||
| chr4:86654223
|
A | G | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.116-18142A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86654223 | ||||||
| chr4:86654331
|
A | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-18034A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86654331 | ||||||
| chr4:86654350
|
T | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-18015T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86654350 | ||||||
| chr4:86654849
|
T | C | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.116-17516T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86654849 | ||||||
| chr4:86654940
|
A | G | 1 | a0003c0002t0005g0169 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.116-17425A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86654940 | ||||||
| chr4:86654986
|
C | G | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.116-17379C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86654986 | ||||||
| chr4:86655185
|
T | C | 9 | a0003c0002t0002g0007a0003c0002t0002g0012a0004c0005t0004g0001others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.116-17180T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86655185 | ||||||
| chr4:86655231
|
G | T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.116-17134G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86655231 | ||||||
| chr4:86655329
|
C | T | 1 | a0003c0002t0001g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.116-17036C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86655329 | ||||||
| chr4:86655357
|
C | T | 1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.116-17008C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86655357 | ||||||
| chr4:86655432
|
G | A | 1 | a0002c0001t0002g0105 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.116-16933G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86655432 | ||||||
| chr4:86655476
|
G | T | 2 | a0001c0003t0001g0090a0001c0003t0001g0093 | 2 | HG01074.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.116-16889G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86655476 | ||||||
| chr4:86655531
|
G | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.116-16834G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86655531 | ||||||
| chr4:86655567
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.116-16798G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86655567 | ||||||
| chr4:86655755
|
A | G | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.116-16610A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86655755 | ||||||
| chr4:86655780
|
C | T | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-16585C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86655780 | ||||||
| chr4:86656034
|
C | T | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-16331C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86656034 | ||||||
| chr4:86656367
|
C | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-15998C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86656367 | ||||||
| chr4:86656396
|
A | T | 1 | a0003c0002t0001g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.116-15969A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86656396 | ||||||
| chr4:86656404
|
G | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-15961G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86656404 | ||||||
| chr4:86656664
|
C | T | 1 | a0003c0002t0001g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.116-15701C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86656664 | ||||||
| chr4:86656700
|
T | C | 174 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.116-15665T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86656700 | ||||||
| chr4:86656939
|
C | T | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-15426C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86656939 | ||||||
| chr4:86657007
|
C | A | 1 | a0003c0002t0001g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.116-15358C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86657007 | ||||||
| chr4:86657235
|
G | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-15130G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86657235 | ||||||
| chr4:86657307
|
G | A | 2 | a0003c0002t0002g0014a0003c0002t0002g0017 | 2 | HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.116-15058G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86657307 | ||||||
| chr4:86657436
|
C | G | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.116-14929C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86657436 | ||||||
| chr4:86657571
|
A | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-14794A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86657571 | ||||||
| chr4:86657877
|
A | G | 197 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.116-14488A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86657877 | ||||||
| chr4:86657963
|
C | T | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.116-14402C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86657963 | ||||||
| chr4:86658011
|
C | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-14354C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86658011 | ||||||
| chr4:86658322
|
C | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-14043C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86658322 | ||||||
| chr4:86658813
|
T | A | 2 | a0002c0001t0002g0129a0002c0001t0002g0130 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.116-13552T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86658813 | ||||||
| chr4:86658877
|
G | T | 1 | a0005c0008t0002g0161 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.116-13488G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86658877 | ||||||
| chr4:86659138
|
T | G | 1 | a0002c0001t0002g0111 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.116-13227T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86659138 | ||||||
| chr4:86659144
|
A | G | 71 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(68): Show | 71 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.116-13221A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86659144 | ||||||
| chr4:86659222
|
A | G | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.116-13143A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86659222 | ||||||
| chr4:86659285
|
A | C | 4 | a0008c0014t0003g0025a0008c0014t0003g0026a0008c0032t0003g0028others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-13080A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86659285 | ||||||
| chr4:86659336
|
TCA | T | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.116-13028_116-1302 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86659336 | ||||||
| chr4:86659659
|
T | TA | 3 | a0002c0011t0001g0113a0002c0011t0002g0112a0002c0011t0002g0124 | 3 | NA18953.hp1 NA18959.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.116-12705dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86659659 | |||||
| chr4:86659685
|
G | A | 3 | a0004c0005t0005g0076a0004c0005t0005g0084a0004c0028t0005g0077 | 3 | HG00738.hp2 HG01099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.116-12680G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86659685 | ||||||
| chr4:86659757
|
G | A | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-12608G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86659757 | ||||||
| chr4:86659841
|
GA | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-12512delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86659841 | |||||
| chr4:86659853
|
A | G | 1 | a0001c0004t0001g0074 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.116-12512A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86659853 | ||||||
| chr4:86659866
|
A | C | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.116-12499A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86659866 | ||||||
| chr4:86660049
|
A | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.116-12316A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86660049 | ||||||
| chr4:86660290
|
A | T | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.116-12075A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86660290 | ||||||
| chr4:86660401
|
T | C | 1 | a0007c0007t0004g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.116-11964T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86660401 | ||||||
| chr4:86660405
|
T | A | 13 | a0003c0002t0002g0007a0003c0006t0003g0021a0003c0006t0003g0022others(10): Show | 13 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.116-11960T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86660405 | ||||||
| chr4:86660406
|
A | T | 2 | a0003c0002t0001g0170a0003c0002t0001g0173 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.116-11959A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86660406 | ||||||
| chr4:86661267
|
T | C | 2 | a0003c0009t0002g0144a0013c0029t0002g0145 | 2 | HG01099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.116-11098T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86661267 | ||||||
| chr4:86661770
|
A | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-10595A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86661770 | ||||||
| chr4:86662002
|
A | C | 1 | a0002c0001t0002g0138 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.116-10363A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86662002 | ||||||
| chr4:86662101
|
T | C | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-10264T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86662101 | ||||||
| chr4:86662414
|
C | A | 3 | a0008c0014t0003g0025a0008c0014t0003g0026a0022c0031t0003g0027 | 3 | HG02145.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.116-9951C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86662414 | ||||||
| chr4:86662418
|
G | C | 2 | a0003c0002t0001g0091a0003c0002t0001g0190 | 2 | NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.116-9947G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86662418 | ||||||
| chr4:86662566
|
A | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-9799A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86662566 | ||||||
| chr4:86662633
|
A | T | 1 | a0002c0001t0002g0159 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.116-9732A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86662633 | ||||||
| chr4:86662670
|
G | T | 88 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(85): Show | 88 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.116-9695G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86662670 | ||||||
| chr4:86662764
|
A | T | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-9601A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86662764 | ||||||
| chr4:86663383
|
C | T | 1 | a0002c0001t0002g0159 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.116-8982C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86663383 | ||||||
| chr4:86663792
|
T | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-8573T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86663792 | ||||||
| chr4:86664033
|
T | C | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-8332T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86664033 | ||||||
| chr4:86664171
|
C | T | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-8194C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86664171 | ||||||
| chr4:86664282
|
A | G | 1 | a0004c0028t0005g0077 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.116-8083A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86664282 | ||||||
| chr4:86664403
|
T | G | 1 | a0004c0005t0004g0002 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.116-7962T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86664403 | ||||||
| chr4:86664702
|
G | A | 8 | a0001c0003t0001g0088a0001c0003t0001g0089a0001c0003t0001g0090others(5): Show | 8 | HG01074.hp2 HG01993.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-7663G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86664702 | ||||||
| chr4:86665391
|
T | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-6974T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86665391 | ||||||
| chr4:86665628
|
T | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-6737T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86665628 | ||||||
| chr4:86665757
|
G | C | 1 | a0002c0001t0002g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.116-6608G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86665757 | ||||||
| chr4:86665847
|
G | T | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-6518G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86665847 | ||||||
| chr4:86666029
|
C | A | 1 | a0001c0004t0001g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.116-6336C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86666029 | ||||||
| chr4:86666284
|
G | C | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.116-6081G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86666284 | ||||||
| chr4:86666295
|
G | A | 2 | a0012c0016t0006g0198a0013c0029t0002g0145 | 2 | HG01346.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.116-6070G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86666295 | ||||||
| chr4:86666311
|
C | CATCAAG | 197 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.116-6052_116-6051i others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86666311 | |||||
| chr4:86666324
|
G | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-6041G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86666324 | ||||||
| chr4:86666330
|
C | T | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-6035C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86666330 | ||||||
| chr4:86666385
|
C | T | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.116-5980C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86666385 | ||||||
| chr4:86666387
|
GCTCTCTC others(2): Show |
G | 3 | a0003c0002t0002g0010a0010c0013t0003g0011a0010c0013t0003g0018 | 3 | HG01243.hp1 HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.116-5951_116-5943d others(11): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86666387 | |||||
| chr4:86666408
|
C | G | 1 | a0003c0002t0001g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.116-5957C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86666408 | ||||||
| chr4:86666414
|
T | C | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-5951T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86666414 | ||||||
| chr4:86666430
|
G | T | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.116-5935G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86666430 | ||||||
| chr4:86666548
|
T | A | 1 | a0001c0004t0001g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.116-5817T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86666548 | ||||||
| chr4:86666611
|
T | G | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.116-5754T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86666611 | ||||||
| chr4:86666793
|
G | A | 1 | a0002c0001t0002g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.116-5572G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86666793 | ||||||
| chr4:86666958
|
T | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-5407T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86666958 | ||||||
| chr4:86667014
|
T | C | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.116-5351T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86667014 | ||||||
| chr4:86667097
|
A | G | 1 | a0005c0008t0002g0150 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.116-5268A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86667097 | ||||||
| chr4:86667256
|
T | C | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.116-5109T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86667256 | ||||||
| chr4:86667378
|
T | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-4987T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86667378 | ||||||
| chr4:86667651
|
A | G | 1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.116-4714A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86667651 | ||||||
| chr4:86667674
|
G | T | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.116-4691G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86667674 | ||||||
| chr4:86667779
|
T | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-4586T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86667779 | ||||||
| chr4:86668038
|
T | C | 1 | a0008c0032t0003g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.116-4327T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86668038 | ||||||
| chr4:86668646
|
AGTGCAGT others(3): Show |
A | 2 | a0002c0001t0002g0156a0002c0001t0002g0157 | 2 | NA18968.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.116-3715_116-3706d others(12): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86668646 | |||||
| chr4:86668762
|
A | AT | 10 | a0001c0003t0001g0037a0001c0004t0001g0070a0003c0002t0001g0098others(7): Show | 10 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.116-3579dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86668762 | |||||
| chr4:86668762
|
AT | A | 77 | a0001c0003t0001g0038a0001c0003t0001g0092a0001c0003t0001g0093others(74): Show | 77 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.116-3579delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86668762 | |||||
| chr4:86668851
|
C | T | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-3514C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86668851 | ||||||
| chr4:86669001
|
T | C | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-3364T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86669001 | ||||||
| chr4:86669097
|
C | A | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.116-3268C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86669097 | ||||||
| chr4:86669150
|
G | C | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.116-3215G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86669150 | ||||||
| chr4:86669285
|
G | GTA | 62 | a0001c0003t0001g0033a0001c0003t0001g0035a0001c0003t0001g0037others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.116-3049_116-3048d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86669285 | |||||
| chr4:86669285
|
G | GTATA | 12 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0088others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.116-3051_116-3048d others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86669285 | |||||
| chr4:86669285
|
G | GTATATA | 10 | a0001c0003t0001g0034a0001c0003t0001g0038a0001c0003t0001g0044others(7): Show | 10 | HG01081.hp2 HG03225.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.116-3053_116-3048d others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86669285 | |||||
| chr4:86669285
|
G | GTATATAT others(1): Show |
6 | a0001c0003t0001g0060a0001c0003t0001g0061a0001c0003t0001g0093others(3): Show | 6 | HG01175.hp1 HG01993.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-3055_116-3048d others(10): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86669285 | |||||
| chr4:86669285
|
G | GTATATAT others(3): Show |
2 | a0001c0003t0001g0062a0003c0002t0001g0173 | 2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.116-3057_116-3048d others(12): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86669285 | |||||
| chr4:86669285
|
G | GTATATAT others(7): Show |
1 | a0001c0003t0002g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.116-3061_116-3048d others(16): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86669285 | |||||
| chr4:86669285
|
G | GTATATAT others(13): Show |
1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.116-3067_116-3048d others(22): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86669285 | |||||
| chr4:86669285
|
GTA | G | 8 | a0002c0001t0002g0110a0002c0001t0002g0147a0002c0001t0002g0154others(5): Show | 8 | HG00609.hp2 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-3049_116-3048d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86669285 | |||||
| chr4:86669285
|
GTATA | G | 62 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(59): Show | 62 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.116-3051_116-3048d others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86669285 | |||||
| chr4:86669285
|
GTATATA | G | 5 | a0003c0002t0002g0015a0003c0002t0002g0016a0004c0005t0004g0009others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-3053_116-3048d others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86669285 | |||||
| chr4:86669285
|
GTATATAT others(11): Show |
G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-3065_116-3048d others(20): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86669285 | |||||
| chr4:86669440
|
G | A | 1 | a0007c0007t0004g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.116-2925G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86669440 | ||||||
| chr4:86669551
|
G | A | 1 | a0003c0002t0009g0188 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.116-2814G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86669551 | ||||||
| chr4:86669608
|
T | C | 3 | a0006c0010t0003g0194a0006c0010t0003g0195a0006c0010t0003g0196 | 3 | HG02486.hp1 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.116-2757T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86669608 | ||||||
| chr4:86669647
|
G | A | 1 | a0007c0007t0004g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.116-2718G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86669647 | ||||||
| chr4:86669663
|
T | C | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-2702T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86669663 | ||||||
| chr4:86669993
|
G | C | 1 | a0002c0001t0002g0157 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.116-2372G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86669993 | ||||||
| chr4:86670171
|
CTT | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-2178_116-2177d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr4 | 86670171 | |||||
| chr4:86670243
|
C | G | 1 | a0002c0001t0002g0120 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.116-2122C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86670243 | ||||||
| chr4:86670626
|
C | T | 3 | a0008c0014t0003g0025a0008c0014t0003g0026a0022c0031t0003g0027 | 3 | HG02145.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.116-1739C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86670626 | ||||||
| chr4:86670649
|
T | C | 1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.116-1716T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86670649 | ||||||
| chr4:86670706
|
G | A | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-1659G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86670706 | ||||||
| chr4:86670708
|
T | C | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-1657T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86670708 | ||||||
| chr4:86670937
|
A | G | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.116-1428A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86670937 | ||||||
| chr4:86671531
|
G | A | 1 | a0017c0022t0002g0114 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.116-834G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86671531 | ||||||
| chr4:86671759
|
C | T | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-606C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86671759 | ||||||
| chr4:86671805
|
C | T | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-560C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86671805 | ||||||
| chr4:86671963
|
A | G | 3 | a0003c0002t0001g0099a0003c0002t0001g0100a0003c0002t0001g0101 | 3 | HG02451.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.116-402A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86671963 | ||||||
| chr4:86671986
|
A | G | 1 | a0001c0018t0001g0078 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.116-379A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 2/47 | chr4 | 86671986 | ||||||
| chr4:86672724
|
T | C | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.294+181T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86672724 | ||||||
| chr4:86672747
|
A | G | 9 | a0003c0002t0002g0007a0003c0002t0002g0012a0004c0005t0004g0001others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.294+204A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86672747 | ||||||
| chr4:86672804
|
C | T | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+261C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86672804 | ||||||
| chr4:86672902
|
G | C | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.294+359G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86672902 | ||||||
| chr4:86673049
|
A | G | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.294+506A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86673049 | ||||||
| chr4:86673319
|
G | T | 60 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.294+776G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86673319 | ||||||
| chr4:86673321
|
T | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.294+778T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86673321 | ||||||
| chr4:86673751
|
A | G | 1 | a0001c0004t0001g0181 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.294+1208A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86673751 | ||||||
| chr4:86673931
|
T | G | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+1388T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86673931 | ||||||
| chr4:86674157
|
A | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+1614A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86674157 | ||||||
| chr4:86674295
|
A | C | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.294+1752A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86674295 | ||||||
| chr4:86674504
|
G | C | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.294+1961G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86674504 | ||||||
| chr4:86674669
|
G | A | 5 | a0001c0003t0001g0079a0001c0003t0001g0080a0001c0003t0001g0081others(2): Show | 5 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+2126G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86674669 | ||||||
| chr4:86674802
|
A | G | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.294+2259A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86674802 | ||||||
| chr4:86675190
|
A | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.294+2647A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86675190 | ||||||
| chr4:86675412
|
G | A | 3 | a0003c0002t0001g0099a0003c0002t0001g0100a0003c0002t0001g0101 | 3 | HG02451.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.294+2869G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86675412 | ||||||
| chr4:86675414
|
G | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+2871G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86675414 | ||||||
| chr4:86675490
|
T | C | 1 | a0006c0010t0003g0196 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.294+2947T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86675490 | ||||||
| chr4:86675537
|
A | C | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.294+2994A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86675537 | ||||||
| chr4:86675629
|
A | G | 1 | a0019c0024t0004g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.294+3086A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86675629 | ||||||
| chr4:86676302
|
T | C | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.294+3759T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86676302 | ||||||
| chr4:86676638
|
A | T | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.294+4095A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86676638 | ||||||
| chr4:86676942
|
C | T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.294+4399C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86676942 | ||||||
| chr4:86677006
|
G | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.294+4463G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86677006 | ||||||
| chr4:86677041
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.294+4498G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86677041 | ||||||
| chr4:86677136
|
G | A | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.294+4593G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86677136 | ||||||
| chr4:86677180
|
T | C | 4 | a0004c0005t0004g0001a0004c0005t0004g0003a0004c0005t0004g0004others(1): Show | 4 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+4637T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86677180 | ||||||
| chr4:86677214
|
C | T | 1 | a0006c0010t0003g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.294+4671C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86677214 | ||||||
| chr4:86677221
|
C | T | 4 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(1): Show | 4 | HG02486.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+4678C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86677221 | ||||||
| chr4:86677318
|
CTT | C | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+4789_294+4790d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr4 | 86677318 | |||||
| chr4:86677378
|
G | C | 14 | a0002c0001t0002g0133a0002c0001t0002g0134a0002c0001t0002g0135others(11): Show | 14 | HG02135.hp2 NA18612.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.294+4835G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86677378 | ||||||
| chr4:86677509
|
C | A | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.294+4966C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86677509 | ||||||
| chr4:86677539
|
G | A | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.294+4996G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86677539 | ||||||
| chr4:86677634
|
GT | G | 10 | a0001c0004t0001g0075a0003c0002t0002g0007a0004c0005t0004g0001others(7): Show | 10 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.294+5106delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr4 | 86677634 | |||||
| chr4:86677649
|
T | C | 1 | a0002c0001t0002g0148 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.294+5106T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86677649 | ||||||
| chr4:86677906
|
G | A | 1 | a0003c0002t0001g0168 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.294+5363G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86677906 | ||||||
| chr4:86678332
|
C | T | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.294+5789C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86678332 | ||||||
| chr4:86678386
|
A | G | 9 | a0003c0002t0002g0007a0003c0002t0002g0012a0004c0005t0004g0001others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.294+5843A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86678386 | ||||||
| chr4:86678478
|
A | T | 1 | a0002c0001t0002g0127 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.294+5935A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86678478 | ||||||
| chr4:86678499
|
C | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+5956C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86678499 | ||||||
| chr4:86679048
|
T | G | 9 | a0003c0002t0002g0007a0003c0002t0002g0012a0004c0005t0004g0001others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.294+6505T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86679048 | ||||||
| chr4:86679224
|
G | C | 9 | a0003c0002t0002g0007a0003c0002t0002g0012a0004c0005t0004g0001others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.294+6681G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86679224 | ||||||
| chr4:86679482
|
G | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.294+6939G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86679482 | ||||||
| chr4:86679695
|
T | C | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.295-7015T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86679695 | ||||||
| chr4:86679748
|
A | G | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.295-6962A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86679748 | ||||||
| chr4:86680256
|
T | C | 9 | a0003c0002t0002g0007a0003c0002t0002g0012a0004c0005t0004g0001others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.295-6454T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86680256 | ||||||
| chr4:86680347
|
C | CTCTA | 29 | a0001c0003t0001g0033a0001c0003t0001g0062a0001c0004t0001g0069others(26): Show | 29 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.295-6311_295-6308d others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr4 | 86680347 | |||||
| chr4:86680347
|
C | CTCTATCT others(1): Show |
3 | a0001c0004t0001g0176a0002c0001t0002g0142a0003c0002t0001g0171 | 3 | HG02615.hp1 NA18906.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.295-6315_295-6308d others(10): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr4 | 86680347 | |||||
| chr4:86680347
|
C | CTCTATCT others(5): Show |
1 | a0001c0003t0001g0079 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.295-6319_295-6308d others(14): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr4 | 86680347 | |||||
| chr4:86680347
|
CTCTA | C | 85 | a0001c0003t0001g0034a0001c0003t0001g0035a0001c0003t0001g0044others(82): Show | 85 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.295-6311_295-6308d others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr4 | 86680347 | |||||
| chr4:86680347
|
CTCTATCT others(1): Show |
C | 30 | a0001c0003t0001g0059a0001c0003t0001g0061a0001c0003t0001g0065others(27): Show | 30 | HG00438.hp1 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.295-6315_295-6308d others(10): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr4 | 86680347 | |||||
| chr4:86680347
|
CTCTATCT others(9): Show |
C | 1 | a0002c0001t0002g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.295-6323_295-6308d others(18): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr4 | 86680347 | |||||
| chr4:86680559
|
G | A | 5 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(2): Show | 5 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-6151G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86680559 | ||||||
| chr4:86680658
|
A | G | 14 | a0001c0004t0001g0181a0003c0002t0001g0091a0003c0002t0001g0180others(11): Show | 14 | HG00438.hp2 HG01071.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.295-6052A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86680658 | ||||||
| chr4:86680836
|
G | A | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.295-5874G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86680836 | ||||||
| chr4:86681033
|
G | GTGATGA | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-5665_295-5660d others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr4 | 86681033 | |||||
| chr4:86681618
|
G | T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.295-5092G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86681618 | ||||||
| chr4:86681650
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.295-5060G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86681650 | ||||||
| chr4:86681861
|
G | A | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.295-4849G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86681861 | ||||||
| chr4:86682425
|
CT | C | 12 | a0001c0003t0001g0080a0003c0002t0002g0012a0003c0002t0002g0014others(9): Show | 12 | HG01123.hp2 HG01168.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.295-4271delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr4 | 86682425 | |||||
| chr4:86682465
|
C | T | 2 | a0001c0004t0001g0053a0004c0005t0004g0002 | 2 | HG01346.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.295-4245C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86682465 | ||||||
| chr4:86682603
|
C | T | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.295-4107C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86682603 | ||||||
| chr4:86682770
|
G | A | 1 | a0002c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.295-3940G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86682770 | ||||||
| chr4:86682776
|
A | G | 3 | a0004c0005t0005g0076a0004c0005t0005g0084a0004c0028t0005g0077 | 3 | HG00738.hp2 HG01099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.295-3934A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86682776 | ||||||
| chr4:86682787
|
G | T | 92 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.295-3923G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86682787 | ||||||
| chr4:86682839
|
T | C | 9 | a0003c0002t0002g0007a0003c0002t0002g0012a0004c0005t0004g0001others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.295-3871T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86682839 | ||||||
| chr4:86682882
|
G | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-3828G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86682882 | ||||||
| chr4:86683081
|
A | G | 1 | a0001c0027t0001g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.295-3629A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86683081 | ||||||
| chr4:86683150
|
CGT | C | 16 | a0003c0002t0002g0007a0003c0002t0002g0010a0003c0002t0002g0012others(13): Show | 16 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.295-3539_295-3538d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr4 | 86683150 | |||||
| chr4:86683479
|
G | A | 1 | a0010c0013t0003g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.295-3231G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86683479 | ||||||
| chr4:86683479
|
G | T | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.295-3231G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86683479 | ||||||
| chr4:86684022
|
T | C | 2 | a0003c0002t0001g0170a0003c0002t0001g0173 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.295-2688T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86684022 | ||||||
| chr4:86684100
|
T | TAAAA | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-2599_295-2596d others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr4 | 86684100 | |||||
| chr4:86684118
|
G | A | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.295-2592G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86684118 | ||||||
| chr4:86684182
|
T | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-2528T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86684182 | ||||||
| chr4:86684337
|
C | T | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.295-2373C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86684337 | ||||||
| chr4:86684363
|
A | T | 1 | a0002c0001t0002g0147 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.295-2347A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86684363 | ||||||
| chr4:86684384
|
C | T | 42 | a0001c0003t0001g0035a0001c0003t0001g0037a0001c0003t0001g0038others(39): Show | 42 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.295-2326C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86684384 | ||||||
| chr4:86684810
|
T | C | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.295-1900T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86684810 | ||||||
| chr4:86684863
|
G | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.295-1847G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86684863 | ||||||
| chr4:86684921
|
A | G | 3 | a0002c0001t0002g0129a0002c0001t0002g0130a0002c0001t0002g0131 | 3 | HG00280.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.295-1789A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86684921 | ||||||
| chr4:86685366
|
C | T | 1 | a0005c0008t0002g0152 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.295-1344C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86685366 | ||||||
| chr4:86685439
|
T | C | 1 | a0007c0007t0004g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.295-1271T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86685439 | ||||||
| chr4:86685662
|
T | C | 1 | a0002c0001t0002g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.295-1048T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86685662 | ||||||
| chr4:86685702
|
A | G | 1 | a0001c0004t0002g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.295-1008A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86685702 | ||||||
| chr4:86685711
|
G | A | 1 | a0003c0002t0001g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.295-999G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86685711 | ||||||
| chr4:86685730
|
A | G | 61 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(58): Show | 61 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.295-980A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86685730 | ||||||
| chr4:86685816
|
A | G | 1 | a0001c0003t0001g0033 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.295-894A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86685816 | ||||||
| chr4:86685947
|
C | A | 3 | a0006c0010t0003g0194a0006c0010t0003g0195a0006c0010t0003g0196 | 3 | HG02486.hp1 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.295-763C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86685947 | ||||||
| chr4:86686359
|
A | C | 4 | a0008c0014t0003g0025a0008c0014t0003g0026a0008c0032t0003g0028others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-351A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86686359 | ||||||
| chr4:86686383
|
T | A | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-327T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 3/47 | chr4 | 86686383 | ||||||
| chr4:86686881
|
G | A | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+106G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86686881 | ||||||
| chr4:86687275
|
T | C | 4 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(1): Show | 4 | HG02486.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+500T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86687275 | ||||||
| chr4:86687442
|
C | G | 1 | a0002c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.360+667C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86687442 | ||||||
| chr4:86687666
|
T | C | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+891T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86687666 | ||||||
| chr4:86687908
|
G | A | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.361-1097G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86687908 | ||||||
| chr4:86688167
|
C | T | 64 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(61): Show | 64 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.361-838C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86688167 | ||||||
| chr4:86688422
|
C | T | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.361-583C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86688422 | ||||||
| chr4:86688451
|
T | A | 4 | a0003c0002t0001g0096a0003c0002t0001g0097a0003c0002t0001g0098others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-554T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86688451 | ||||||
| chr4:86688479
|
A | T | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.361-526A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86688479 | ||||||
| chr4:86688519
|
A | G | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.361-486A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86688519 | ||||||
| chr4:86688552
|
A | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.361-453A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86688552 | ||||||
| chr4:86688692
|
T | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.361-313T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86688692 | ||||||
| chr4:86688835
|
A | T | 1 | a0001c0003t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.361-170A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86688835 | ||||||
| chr4:86688977
|
C | T | 1 | a0003c0002t0001g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.361-28C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 4/47 | chr4 | 86688977 | ||||||
| chr4:86689223
|
T | A | 2 | a0003c0002t0002g0007a0019c0024t0004g0008 | 2 | HG00639.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.546+33T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86689223 | ||||||
| chr4:86689401
|
A | T | 6 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(3): Show | 6 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.546+211A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86689401 | ||||||
| chr4:86689636
|
C | T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.546+446C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86689636 | ||||||
| chr4:86689645
|
C | A | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.546+455C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86689645 | ||||||
| chr4:86689656
|
G | A | 8 | a0003c0002t0002g0007a0003c0002t0009g0188a0004c0005t0004g0001others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.546+466G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86689656 | ||||||
| chr4:86690033
|
G | A | 1 | a0002c0001t0002g0153 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.546+843G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86690033 | ||||||
| chr4:86690443
|
A | G | 4 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0086others(1): Show | 4 | NA18947.hp1 NA19003.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+1253A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86690443 | ||||||
| chr4:86690495
|
T | A | 1 | a0003c0002t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.546+1305T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86690495 | ||||||
| chr4:86690648
|
A | G | 1 | a0002c0001t0002g0157 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.546+1458A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86690648 | ||||||
| chr4:86690742
|
AT | A | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.546+1560delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr4 | 86690742 | |||||
| chr4:86691337
|
A | G | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.546+2147A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86691337 | ||||||
| chr4:86691356
|
C | T | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.546+2166C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86691356 | ||||||
| chr4:86691734
|
G | T | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.547-1853G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86691734 | ||||||
| chr4:86692059
|
T | C | 93 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(90): Show | 93 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.547-1528T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86692059 | ||||||
| chr4:86692242
|
G | A | 61 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(58): Show | 61 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.547-1345G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86692242 | ||||||
| chr4:86692278
|
T | C | 1 | a0001c0018t0001g0078 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.547-1309T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86692278 | ||||||
| chr4:86692508
|
C | G | 1 | a0003c0002t0001g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.547-1079C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86692508 | ||||||
| chr4:86692666
|
T | C | 3 | a0008c0014t0003g0025a0008c0014t0003g0026a0022c0031t0003g0027 | 3 | HG02145.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.547-921T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86692666 | ||||||
| chr4:86692701
|
A | C | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.547-886A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86692701 | ||||||
| chr4:86692738
|
A | G | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.547-849A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86692738 | ||||||
| chr4:86693057
|
G | T | 4 | a0003c0002t0003g0193a0006c0010t0003g0194a0006c0010t0003g0195others(1): Show | 4 | HG02486.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-530G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86693057 | ||||||
| chr4:86693071
|
T | TAAAAAAA others(1): Show |
5 | a0003c0002t0002g0007a0004c0005t0004g0003a0004c0005t0004g0004others(2): Show | 5 | HG00639.hp1 HG01123.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-501_547-494dup others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr4 | 86693071 | |||||
| chr4:86693071
|
TA | T | 102 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(99): Show | 102 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.547-494delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr4 | 86693071 | |||||
| chr4:86693071
|
TAAAAAAA others(4): Show |
T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.547-504_547-494del others(11): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr4 | 86693071 | |||||
| chr4:86693083
|
A | T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.547-504A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86693083 | ||||||
| chr4:86693196
|
C | A | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.547-391C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 5/47 | chr4 | 86693196 | ||||||
| chr4:86693943
|
T | G | 1 | a0006c0010t0003g0196 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.634+269T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86693943 | ||||||
| chr4:86694011
|
T | TATAC | 2 | a0002c0001t0002g0138a0002c0001t0002g0139 | 2 | NA18985.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.634+339_634+340ins others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr4 | 86694011 | |||||
| chr4:86694015
|
T | TTTATGAA others(4): Show |
2 | a0002c0001t0002g0138a0002c0001t0002g0139 | 2 | NA18985.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.634+351_634+352ins others(11): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr4 | 86694015 | |||||
| chr4:86694057
|
G | A | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.634+383G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86694057 | ||||||
| chr4:86694107
|
A | T | 1 | a0008c0032t0003g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.634+433A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86694107 | ||||||
| chr4:86694226
|
T | C | 1 | a0003c0002t0009g0188 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.634+552T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86694226 | ||||||
| chr4:86694437
|
G | T | 4 | a0003c0002t0003g0193a0006c0010t0003g0194a0006c0010t0003g0195others(1): Show | 4 | HG02486.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+763G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86694437 | ||||||
| chr4:86694501
|
C | T | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.634+827C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86694501 | ||||||
| chr4:86694579
|
C | CA | 10 | a0001c0003t0001g0037a0001c0003t0001g0061a0001c0003t0001g0085others(7): Show | 10 | HG01175.hp1 HG02976.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.634+930dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr4 | 86694579 | |||||
| chr4:86694579
|
C | CAA | 9 | a0003c0002t0002g0007a0003c0002t0002g0015a0004c0005t0004g0001others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.634+929_634+930dup others(2): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr4 | 86694579 | |||||
| chr4:86694579
|
CA | C | 11 | a0001c0003t0001g0059a0001c0003t0001g0090a0002c0001t0002g0109others(8): Show | 11 | HG01074.hp2 HG01168.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.634+930delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr4 | 86694579 | |||||
| chr4:86694788
|
T | A | 1 | a0004c0005t0004g0003 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.634+1114T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86694788 | ||||||
| chr4:86695515
|
C | CAG | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.634+1842_634+1843i others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr4 | 86695515 | |||||
| chr4:86695576
|
T | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+1902T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86695576 | ||||||
| chr4:86695717
|
G | C | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.634+2043G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86695717 | ||||||
| chr4:86695845
|
T | C | 1 | a0001c0004t0002g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.634+2171T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86695845 | ||||||
| chr4:86696041
|
A | G | 1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.634+2367A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86696041 | ||||||
| chr4:86696291
|
T | C | 1 | a0002c0001t0002g0106 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.634+2617T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86696291 | ||||||
| chr4:86696343
|
A | G | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.634+2669A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86696343 | ||||||
| chr4:86697792
|
T | C | 1 | a0001c0004t0001g0072 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.635-3449T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86697792 | ||||||
| chr4:86697896
|
T | TTTTTCTA others(13): Show |
8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.635-3344_635-3325d others(22): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr4 | 86697896 | |||||
| chr4:86698203
|
T | C | 1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.635-3038T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86698203 | ||||||
| chr4:86698204
|
A | G | 4 | a0003c0002t0003g0193a0006c0010t0003g0194a0006c0010t0003g0195others(1): Show | 4 | HG02486.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-3037A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86698204 | ||||||
| chr4:86698211
|
TTAAA | T | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.635-3026_635-3023d others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr4 | 86698211 | |||||
| chr4:86698405
|
T | C | 3 | a0002c0001t0002g0104a0002c0001t0002g0156a0002c0001t0002g0157 | 3 | HG04115.hp2 NA18968.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.635-2836T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86698405 | ||||||
| chr4:86698598
|
T | G | 1 | a0001c0004t0001g0074 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.635-2643T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86698598 | ||||||
| chr4:86698730
|
A | G | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-2511A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86698730 | ||||||
| chr4:86699052
|
C | G | 2 | a0002c0001t0002g0148a0002c0001t0002g0153 | 2 | HG02129.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.635-2189C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86699052 | ||||||
| chr4:86699254
|
T | C | 1 | a0008c0032t0003g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.635-1987T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86699254 | ||||||
| chr4:86699355
|
G | C | 1 | a0001c0004t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.635-1886G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86699355 | ||||||
| chr4:86699447
|
C | G | 3 | a0008c0014t0003g0025a0008c0014t0003g0026a0022c0031t0003g0027 | 3 | HG02145.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.635-1794C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86699447 | ||||||
| chr4:86699580
|
CAT | C | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-1660_635-1659d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86699580 | ||||||
| chr4:86699621
|
T | A | 4 | a0003c0002t0001g0168a0003c0002t0001g0171a0003c0002t0001g0172others(1): Show | 4 | HG01243.hp2 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-1620T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86699621 | ||||||
| chr4:86699720
|
A | G | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-1521A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86699720 | ||||||
| chr4:86699802
|
T | C | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.635-1439T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86699802 | ||||||
| chr4:86699836
|
C | T | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-1405C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86699836 | ||||||
| chr4:86700223
|
TTTATTA | T | 3 | a0008c0014t0003g0025a0008c0014t0003g0026a0022c0031t0003g0027 | 3 | HG02145.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.635-1011_635-1006d others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr4 | 86700223 | |||||
| chr4:86700242
|
T | C | 1 | a0002c0001t0002g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.635-999T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86700242 | ||||||
| chr4:86700320
|
T | C | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.635-921T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86700320 | ||||||
| chr4:86700356
|
G | A | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.635-885G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86700356 | ||||||
| chr4:86700450
|
T | C | 3 | a0002c0011t0001g0113a0002c0011t0002g0112a0002c0011t0002g0124 | 3 | NA18953.hp1 NA18959.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.635-791T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 6/47 | chr4 | 86700450 | ||||||
| chr4:86701833
|
T | C | 4 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(1): Show | 4 | HG02486.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1195+32T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86701833 | ||||||
| chr4:86701869
|
G | A | 1 | a0003c0006t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1195+68G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86701869 | ||||||
| chr4:86701978
|
T | C | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+177T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86701978 | ||||||
| chr4:86702202
|
C | T | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+401C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86702202 | ||||||
| chr4:86702217
|
C | T | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1195+416C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86702217 | ||||||
| chr4:86702354
|
T | A | 1 | a0003c0009t0001g0102 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1195+553T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86702354 | ||||||
| chr4:86702358
|
A | C | 7 | a0003c0002t0001g0096a0003c0002t0001g0097a0003c0002t0001g0098others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195+557A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86702358 | ||||||
| chr4:86702374
|
A | T | 1 | a0002c0011t0001g0113 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1195+573A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86702374 | ||||||
| chr4:86702769
|
C | T | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1195+968C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86702769 | ||||||
| chr4:86702909
|
G | A | 1 | a0001c0004t0001g0181 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1195+1108G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86702909 | ||||||
| chr4:86703048
|
G | A | 1 | a0002c0001t0002g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1195+1247G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86703048 | ||||||
| chr4:86703435
|
G | A | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1195+1634G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86703435 | ||||||
| chr4:86703437
|
G | GA | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+1648dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86703437 | |||||
| chr4:86703437
|
G | T | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1195+1636G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86703437 | ||||||
| chr4:86703438
|
A | G | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1195+1637A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86703438 | ||||||
| chr4:86703527
|
T | TATTTCTA others(2): Show |
15 | a0003c0002t0002g0007a0003c0002t0002g0012a0003c0002t0002g0014others(12): Show | 15 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1195+1730_1195+173 others(13): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86703527 | |||||
| chr4:86703712
|
T | A | 1 | a0004c0005t0005g0076 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1195+1911T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86703712 | ||||||
| chr4:86703729
|
T | C | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1195+1928T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86703729 | ||||||
| chr4:86703745
|
T | C | 3 | a0002c0001t0002g0141a0002c0001t0002g0142a0018c0023t0002g0143 | 3 | HG00642.hp2 HG01361.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1195+1944T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86703745 | ||||||
| chr4:86704092
|
G | A | 2 | a0001c0003t0001g0060a0001c0003t0001g0061 | 2 | HG01175.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1195+2291G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86704092 | ||||||
| chr4:86704141
|
G | A | 3 | a0002c0001t0002g0134a0002c0001t0002g0135a0002c0001t0002g0136 | 3 | NA18944.hp2 NA18948.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1195+2340G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86704141 | ||||||
| chr4:86704208
|
A | G | 1 | a0001c0003t0001g0182 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1195+2407A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86704208 | ||||||
| chr4:86704321
|
G | T | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1195+2520G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86704321 | ||||||
| chr4:86704542
|
T | C | 1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1195+2741T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86704542 | ||||||
| chr4:86704580
|
G | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1195+2779G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86704580 | ||||||
| chr4:86704607
|
C | T | 3 | a0001c0003t0001g0034a0001c0003t0001g0063a0001c0003t0001g0064 | 3 | NA18984.hp2 NA18991.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1195+2806C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86704607 | ||||||
| chr4:86704708
|
C | T | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+2907C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86704708 | ||||||
| chr4:86704875
|
A | G | 36 | a0001c0003t0001g0059a0001c0004t0001g0032a0001c0004t0001g0048others(33): Show | 36 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1195+3074A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86704875 | ||||||
| chr4:86704948
|
A | G | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+3147A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86704948 | ||||||
| chr4:86705045
|
T | G | 4 | a0002c0001t0002g0158a0002c0001t0002g0159a0002c0001t0002g0160others(1): Show | 4 | HG00609.hp2 HG02056.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1195+3244T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86705045 | ||||||
| chr4:86705071
|
G | C | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1195+3270G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86705071 | ||||||
| chr4:86705073
|
T | C | 2 | a0001c0004t0001g0052a0012c0016t0006g0198 | 2 | NA18906.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1195+3272T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86705073 | ||||||
| chr4:86705102
|
A | G | 3 | a0002c0001t0002g0104a0002c0001t0002g0156a0002c0001t0002g0157 | 3 | HG04115.hp2 NA18968.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1195+3301A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86705102 | ||||||
| chr4:86705103
|
G | A | 3 | a0002c0001t0002g0104a0002c0001t0002g0156a0002c0001t0002g0157 | 3 | HG04115.hp2 NA18968.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1195+3302G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86705103 | ||||||
| chr4:86705106
|
C | T | 3 | a0002c0001t0002g0104a0002c0001t0002g0156a0002c0001t0002g0157 | 3 | HG04115.hp2 NA18968.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1195+3305C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86705106 | ||||||
| chr4:86705111
|
A | G | 3 | a0002c0001t0002g0104a0002c0001t0002g0156a0002c0001t0002g0157 | 3 | HG04115.hp2 NA18968.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1195+3310A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86705111 | ||||||
| chr4:86705311
|
G | A | 1 | a0003c0002t0001g0183 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1195+3510G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86705311 | ||||||
| chr4:86705333
|
C | CA | 6 | a0001c0027t0001g0031a0002c0011t0001g0113a0002c0011t0002g0112others(3): Show | 6 | HG00438.hp2 HG02015.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.1195+3547dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86705333 | |||||
| chr4:86705333
|
C | CAAAAAA | 5 | a0002c0001t0002g0134a0002c0001t0002g0139a0003c0009t0002g0144others(2): Show | 5 | HG01099.hp2 HG01243.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195+3542_1195+354 others(10): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86705333 | |||||
| chr4:86705333
|
C | CAAAAAAA | 74 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(71): Show | 74 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1195+3541_1195+354 others(11): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86705333 | |||||
| chr4:86705333
|
C | CAAAAAAA others(1): Show |
10 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(7): Show | 10 | HG00642.hp2 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1195+3540_1195+354 others(12): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86705333 | |||||
| chr4:86705333
|
C | CAAAAAAA others(6): Show |
1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1195+3535_1195+354 others(17): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86705333 | |||||
| chr4:86705333
|
C | CAAAAAAA others(15): Show |
2 | a0004c0005t0004g0002a0004c0005t0004g0003 | 2 | HG01192.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1195+3547_1195+354 others(26): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86705333 | |||||
| chr4:86705333
|
C | CAAAAAAA others(16): Show |
2 | a0004c0005t0004g0004a0004c0005t0004g0005 | 2 | HG01123.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1195+3547_1195+354 others(27): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86705333 | |||||
| chr4:86705333
|
C | CAAAAAAA others(17): Show |
1 | a0004c0005t0004g0001 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1195+3547_1195+354 others(28): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86705333 | |||||
| chr4:86705333
|
C | CAAAAAAA others(18): Show |
1 | a0019c0024t0004g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1195+3547_1195+354 others(29): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86705333 | |||||
| chr4:86705333
|
C | CAAAAAAA others(19): Show |
1 | a0003c0002t0002g0007 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1195+3547_1195+354 others(30): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86705333 | |||||
| chr4:86705445
|
A | G | 1 | a0002c0001t0002g0149 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1195+3644A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86705445 | ||||||
| chr4:86705456
|
G | A | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+3655G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86705456 | ||||||
| chr4:86705460
|
GAGAC | G | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1195+3662_1195+366 others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86705460 | |||||
| chr4:86706166
|
C | G | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1195+4365C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86706166 | ||||||
| chr4:86706555
|
T | C | 1 | a0003c0002t0001g0183 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1195+4754T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86706555 | ||||||
| chr4:86706703
|
G | T | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+4902G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86706703 | ||||||
| chr4:86706725
|
A | G | 1 | a0001c0004t0001g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1195+4924A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86706725 | ||||||
| chr4:86706730
|
G | T | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+4929G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86706730 | ||||||
| chr4:86706767
|
A | G | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+4966A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86706767 | ||||||
| chr4:86706916
|
A | G | 1 | a0004c0005t0004g0005 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1195+5115A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86706916 | ||||||
| chr4:86707136
|
GAGTGAGC | G | 3 | a0004c0005t0005g0076a0004c0005t0005g0084a0004c0028t0005g0077 | 3 | HG00738.hp2 HG01099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1195+5339_1195+534 others(11): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86707136 | |||||
| chr4:86707211
|
A | G | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1195+5410A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86707211 | ||||||
| chr4:86707374
|
T | C | 8 | a0002c0001t0002g0133a0002c0001t0002g0134a0002c0001t0002g0135others(5): Show | 8 | HG02135.hp2 NA18612.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+5573T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86707374 | ||||||
| chr4:86707533
|
C | T | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+5732C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86707533 | ||||||
| chr4:86707616
|
C | G | 1 | a0001c0003t0001g0092 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1195+5815C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86707616 | ||||||
| chr4:86707654
|
C | CTT | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+5853_1195+585 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86707654 | ||||||
| chr4:86707742
|
G | A | 8 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+5941G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86707742 | ||||||
| chr4:86707772
|
A | G | 180 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(177): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1195+5971A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86707772 | ||||||
| chr4:86707866
|
T | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1195+6065T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86707866 | ||||||
| chr4:86708076
|
C | G | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1195+6275C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86708076 | ||||||
| chr4:86708186
|
T | C | 1 | a0003c0002t0001g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1195+6385T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86708186 | ||||||
| chr4:86708361
|
G | A | 1 | a0001c0017t0001g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1195+6560G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86708361 | ||||||
| chr4:86708375
|
CTTCTT | C | 7 | a0003c0002t0002g0007a0004c0005t0004g0001a0004c0005t0004g0002others(4): Show | 7 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1195+6576_1195+658 others(9): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86708375 | |||||
| chr4:86708626
|
A | G | 1 | a0002c0001t0002g0120 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1195+6825A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86708626 | ||||||
| chr4:86708706
|
A | G | 1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1195+6905A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86708706 | ||||||
| chr4:86708784
|
C | T | 9 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1195+6983C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86708784 | ||||||
| chr4:86708983
|
C | T | 7 | a0003c0002t0001g0096a0003c0002t0001g0097a0003c0002t0001g0098others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195+7182C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86708983 | ||||||
| chr4:86709054
|
TACATACA others(5): Show |
T | 1 | a0003c0002t0001g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1195+7269_1195+728 others(16): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86709054 | |||||
| chr4:86709070
|
T | TAC | 2 | a0004c0005t0004g0002a0012c0016t0006g0198 | 2 | HG01346.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1195+7285_1195+728 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86709070 | |||||
| chr4:86709164
|
A | G | 5 | a0003c0002t0002g0010a0007c0007t0004g0132a0007c0007t0004g0167others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1195+7363A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86709164 | ||||||
| chr4:86709237
|
G | A | 14 | a0003c0006t0001g0030a0003c0006t0003g0021a0003c0006t0003g0022others(11): Show | 14 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1196-7293G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86709237 | ||||||
| chr4:86709301
|
T | C | 1 | a0002c0001t0002g0118 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1196-7229T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86709301 | ||||||
| chr4:86709365
|
A | G | 65 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(62): Show | 65 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1196-7165A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86709365 | ||||||
| chr4:86709489
|
A | G | 1 | a0003c0002t0001g0183 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1196-7041A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86709489 | ||||||
| chr4:86709490
|
G | A | 5 | a0003c0006t0001g0030a0003c0006t0010g0029a0008c0014t0003g0025others(2): Show | 5 | HG02717.hp1 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1196-7040G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86709490 | ||||||
| chr4:86709517
|
A | C | 1 | a0002c0001t0002g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1196-7013A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86709517 | ||||||
| chr4:86709687
|
G | A | 5 | a0003c0006t0001g0030a0003c0006t0010g0029a0008c0014t0003g0025others(2): Show | 5 | HG02717.hp1 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1196-6843G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86709687 | ||||||
| chr4:86709770
|
A | G | 1 | a0001c0004t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1196-6760A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86709770 | ||||||
| chr4:86709866
|
A | G | 4 | a0004c0005t0004g0009a0004c0005t0005g0076a0004c0005t0005g0084others(1): Show | 4 | HG00738.hp2 HG01099.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-6664A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86709866 | ||||||
| chr4:86709876
|
AGTTT | A | 91 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1196-6649_1196-664 others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86709876 | |||||
| chr4:86709956
|
T | C | 2 | a0003c0002t0001g0170a0003c0002t0001g0173 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1196-6574T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86709956 | ||||||
| chr4:86710141
|
T | C | 4 | a0004c0005t0004g0009a0004c0005t0005g0076a0004c0005t0005g0084others(1): Show | 4 | HG00738.hp2 HG01099.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-6389T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86710141 | ||||||
| chr4:86710200
|
T | C | 90 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1196-6330T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86710200 | ||||||
| chr4:86710270
|
G | A | 2 | a0003c0002t0002g0014a0003c0002t0002g0017 | 2 | HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1196-6260G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86710270 | ||||||
| chr4:86710379
|
A | G | 4 | a0004c0005t0004g0001a0004c0005t0004g0003a0004c0005t0004g0004others(1): Show | 4 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-6151A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86710379 | ||||||
| chr4:86710738
|
G | T | 4 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(1): Show | 4 | HG02486.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-5792G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86710738 | ||||||
| chr4:86710747
|
G | T | 1 | a0006c0010t0003g0196 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1196-5783G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86710747 | ||||||
| chr4:86711007
|
T | C | 3 | a0003c0002t0001g0186a0003c0002t0001g0187a0003c0002t0009g0188 | 3 | HG01071.hp1 HG01981.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1196-5523T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86711007 | ||||||
| chr4:86711098
|
C | CTTTTTTT others(1): Show |
6 | a0003c0002t0002g0010a0003c0006t0001g0030a0003c0006t0010g0029others(3): Show | 6 | HG02280.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1196-5420_1196-541 others(12): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86711098 | |||||
| chr4:86711098
|
C | CTTTTTTT others(2): Show |
9 | a0003c0002t0002g0016a0003c0006t0003g0021a0003c0006t0003g0023others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1196-5421_1196-541 others(13): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86711098 | |||||
| chr4:86711098
|
C | CTTTTTTT others(3): Show |
8 | a0003c0002t0002g0012a0003c0002t0002g0015a0003c0006t0003g0022others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1196-5422_1196-541 others(14): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86711098 | |||||
| chr4:86711098
|
C | CTTTTTTT others(4): Show |
6 | a0002c0001t0002g0141a0004c0005t0004g0002a0004c0005t0004g0003others(3): Show | 6 | HG01123.hp2 HG01192.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1196-5423_1196-541 others(15): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86711098 | |||||
| chr4:86711098
|
C | CTTTTTTT others(5): Show |
7 | a0002c0001t0002g0108a0002c0001t0002g0133a0002c0001t0002g0142others(4): Show | 7 | HG00642.hp2 HG01175.hp2 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.1196-5424_1196-541 others(16): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86711098 | |||||
| chr4:86711098
|
C | CTTTTTTT others(6): Show |
39 | a0002c0001t0002g0105a0002c0001t0002g0107a0002c0001t0002g0109others(36): Show | 39 | HG00280.hp1 HG00639.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1196-5425_1196-541 others(17): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86711098 | |||||
| chr4:86711098
|
C | CTTTTTTT others(7): Show |
8 | a0002c0001t0002g0122a0002c0001t0002g0151a0002c0001t0002g0155others(5): Show | 8 | HG00140.hp1 HG00609.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.1196-5426_1196-541 others(18): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86711098 | |||||
| chr4:86711098
|
C | CTTTTTTT others(8): Show |
4 | a0002c0001t0002g0111a0002c0001t0002g0157a0003c0002t0002g0014others(1): Show | 4 | HG00423.hp1 HG03041.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-5427_1196-541 others(19): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86711098 | |||||
| chr4:86711098
|
C | CTTTTTTT others(9): Show |
2 | a0002c0001t0002g0146a0002c0001t0002g0160 | 2 | HG00738.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1196-5428_1196-541 others(20): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86711098 | |||||
| chr4:86711098
|
CT | C | 6 | a0001c0003t0001g0062a0001c0003t0002g0006a0001c0004t0002g0126others(3): Show | 6 | HG02559.hp2 HG04228.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1196-5413delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86711098 | |||||
| chr4:86711181
|
A | G | 1 | a0001c0004t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1196-5349A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86711181 | ||||||
| chr4:86711430
|
A | G | 1 | a0002c0001t0002g0137 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1196-5100A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86711430 | ||||||
| chr4:86711443
|
C | T | 1 | a0001c0003t0001g0092 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1196-5087C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86711443 | ||||||
| chr4:86711519
|
G | A | 64 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(61): Show | 64 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1196-5011G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86711519 | ||||||
| chr4:86711669
|
G | C | 2 | a0001c0003t0001g0079a0001c0003t0001g0081 | 2 | HG00140.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1196-4861G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86711669 | ||||||
| chr4:86712231
|
G | A | 58 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1196-4299G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86712231 | ||||||
| chr4:86712348
|
G | T | 6 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(3): Show | 6 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1196-4182G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86712348 | ||||||
| chr4:86712514
|
C | T | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1196-4016C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86712514 | ||||||
| chr4:86712719
|
G | A | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1196-3811G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86712719 | ||||||
| chr4:86713077
|
C | G | 1 | a0001c0003t0001g0038 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1196-3453C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86713077 | ||||||
| chr4:86713077
|
C | T | 4 | a0004c0005t0004g0009a0004c0005t0005g0076a0004c0005t0005g0084others(1): Show | 4 | HG00738.hp2 HG01099.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-3453C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86713077 | ||||||
| chr4:86713486
|
A | G | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1196-3044A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86713486 | ||||||
| chr4:86714068
|
C | CA | 6 | a0002c0001t0002g0104a0002c0001t0002g0160a0007c0007t0004g0132others(3): Show | 6 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1196-2446dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86714068 | |||||
| chr4:86714068
|
CA | C | 25 | a0001c0004t0001g0072a0003c0002t0001g0096a0003c0002t0001g0183others(22): Show | 25 | HG00738.hp2 HG01099.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1196-2446delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr4 | 86714068 | |||||
| chr4:86714173
|
C | T | 1 | a0001c0003t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1196-2357C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86714173 | ||||||
| chr4:86714286
|
T | G | 2 | a0003c0002t0001g0100a0003c0002t0001g0101 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1196-2244T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86714286 | ||||||
| chr4:86714544
|
A | G | 2 | a0008c0014t0003g0025a0008c0014t0003g0026 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1196-1986A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86714544 | ||||||
| chr4:86714774
|
A | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1196-1756A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86714774 | ||||||
| chr4:86714898
|
G | A | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1196-1632G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86714898 | ||||||
| chr4:86715007
|
A | G | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1196-1523A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86715007 | ||||||
| chr4:86715216
|
G | A | 4 | a0004c0005t0004g0009a0004c0005t0005g0076a0004c0005t0005g0084others(1): Show | 4 | HG00738.hp2 HG01099.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-1314G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86715216 | ||||||
| chr4:86715234
|
A | ATG | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1196-1296_1196-129 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86715234 | ||||||
| chr4:86715235
|
C | T | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1196-1295C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86715235 | ||||||
| chr4:86715403
|
G | A | 1 | a0001c0003t0001g0061 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1196-1127G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86715403 | ||||||
| chr4:86715482
|
C | T | 1 | a0006c0010t0003g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1196-1048C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86715482 | ||||||
| chr4:86715498
|
G | A | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1196-1032G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86715498 | ||||||
| chr4:86715759
|
A | G | 1 | a0002c0001t0002g0149 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1196-771A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86715759 | ||||||
| chr4:86715801
|
G | A | 1 | a0002c0001t0002g0148 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1196-729G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86715801 | ||||||
| chr4:86715833
|
A | G | 13 | a0003c0006t0001g0030a0003c0006t0003g0021a0003c0006t0003g0022others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1196-697A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86715833 | ||||||
| chr4:86716054
|
C | A | 1 | a0003c0002t0001g0173 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1196-476C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86716054 | ||||||
| chr4:86716237
|
C | T | 33 | a0003c0002t0002g0010a0003c0002t0002g0014a0003c0002t0002g0015others(30): Show | 33 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.1196-293C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86716237 | ||||||
| chr4:86716363
|
A | G | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1196-167A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86716363 | ||||||
| chr4:86716408
|
A | G | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1196-122A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 7/47 | chr4 | 86716408 | ||||||
| chr4:86716796
|
C | T | 1 | a0002c0001t0002g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1291+171C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 8/47 | chr4 | 86716796 | ||||||
| chr4:86717189
|
A | AT | 127 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0037others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1385+89dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr4 | 86717189 | |||||
| chr4:86717189
|
A | ATT | 11 | a0002c0001t0002g0157a0003c0002t0001g0173a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1385+88_1385+89dup others(2): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr4 | 86717189 | |||||
| chr4:86717211
|
C | T | 58 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1385+94C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86717211 | ||||||
| chr4:86717377
|
T | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1385+260T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86717377 | ||||||
| chr4:86717387
|
C | T | 1 | a0001c0004t0001g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1385+270C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86717387 | ||||||
| chr4:86717498
|
A | C | 13 | a0003c0006t0001g0030a0003c0006t0003g0021a0003c0006t0003g0022others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1385+381A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86717498 | ||||||
| chr4:86717599
|
A | G | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1385+482A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86717599 | ||||||
| chr4:86717910
|
CT | C | 14 | a0001c0004t0001g0072a0003c0006t0001g0030a0003c0006t0003g0021others(11): Show | 14 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1385+801delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr4 | 86717910 | |||||
| chr4:86718007
|
A | G | 2 | a0007c0007t0005g0175a0007c0007t0005g0179 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1385+890A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86718007 | ||||||
| chr4:86718455
|
C | CTTTTTTT others(13): Show |
2 | a0004c0005t0004g0004a0004c0005t0004g0005 | 2 | HG01123.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1385+1351_1385+135 others(24): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr4 | 86718455 | |||||
| chr4:86718455
|
C | CTTTTTTT others(14): Show |
4 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(1): Show | 4 | HG01175.hp2 HG01192.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1385+1351_1385+135 others(25): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr4 | 86718455 | |||||
| chr4:86718455
|
C | CTTTTTTT others(15): Show |
3 | a0004c0005t0005g0076a0004c0005t0005g0084a0004c0028t0005g0077 | 3 | HG00738.hp2 HG01099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1385+1351_1385+135 others(26): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr4 | 86718455 | |||||
| chr4:86718455
|
C | CTTTTTTT others(17): Show |
1 | a0004c0005t0004g0009 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1385+1351_1385+135 others(28): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr4 | 86718455 | |||||
| chr4:86718538
|
T | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1385+1421T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86718538 | ||||||
| chr4:86718681
|
C | T | 57 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(54): Show | 57 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1385+1564C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86718681 | ||||||
| chr4:86718751
|
T | G | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1385+1634T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86718751 | ||||||
| chr4:86719023
|
G | T | 2 | a0003c0002t0002g0015a0003c0002t0002g0016 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1385+1906G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86719023 | ||||||
| chr4:86719278
|
C | T | 1 | a0003c0002t0001g0187 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1385+2161C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86719278 | ||||||
| chr4:86719457
|
C | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1385+2340C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86719457 | ||||||
| chr4:86719575
|
C | T | 1 | a0010c0013t0003g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1385+2458C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86719575 | ||||||
| chr4:86719625
|
C | G | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1385+2508C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86719625 | ||||||
| chr4:86719811
|
T | C | 1 | a0002c0001t0002g0162 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1386-2401T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86719811 | ||||||
| chr4:86719850
|
G | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1386-2362G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86719850 | ||||||
| chr4:86720053
|
T | G | 1 | a0008c0032t0003g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1386-2159T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86720053 | ||||||
| chr4:86720066
|
C | T | 64 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(61): Show | 64 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1386-2146C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86720066 | ||||||
| chr4:86720414
|
G | A | 1 | a0001c0003t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1386-1798G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86720414 | ||||||
| chr4:86720601
|
C | T | 1 | a0007c0007t0004g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1386-1611C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86720601 | ||||||
| chr4:86720777
|
A | C | 1 | a0005c0008t0002g0128 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1386-1435A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86720777 | ||||||
| chr4:86720906
|
C | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1386-1306C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86720906 | ||||||
| chr4:86721208
|
G | A | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1386-1004G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86721208 | ||||||
| chr4:86721237
|
T | C | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386-975T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86721237 | ||||||
| chr4:86721527
|
C | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1386-685C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86721527 | ||||||
| chr4:86721593
|
G | T | 1 | a0004c0005t0004g0002 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1386-619G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86721593 | ||||||
| chr4:86721660
|
TA | T | 2 | a0002c0001t0002g0129a0002c0001t0002g0130 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1386-551delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86721660 | ||||||
| chr4:86721700
|
TCCCTCCC others(11): Show |
T | 58 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1386-503_1386-486d others(20): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr4 | 86721700 | |||||
| chr4:86721703
|
C | T | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1386-509C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86721703 | ||||||
| chr4:86721795
|
G | A | 13 | a0003c0006t0001g0030a0003c0006t0003g0021a0003c0006t0003g0022others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1386-417G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86721795 | ||||||
| chr4:86721844
|
C | G | 7 | a0003c0002t0001g0096a0003c0002t0001g0097a0003c0002t0001g0098others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1386-368C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86721844 | ||||||
| chr4:86721984
|
C | T | 1 | a0001c0003t0001g0092 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1386-228C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86721984 | ||||||
| chr4:86722016
|
G | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1386-196G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86722016 | ||||||
| chr4:86722143
|
A | G | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1386-69A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 9/47 | chr4 | 86722143 | ||||||
| chr4:86722593
|
G | A | 58 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1608+159G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86722593 | ||||||
| chr4:86722975
|
G | C | 11 | a0003c0006t0001g0030a0003c0006t0003g0021a0003c0006t0003g0022others(8): Show | 11 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1608+541G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86722975 | ||||||
| chr4:86722986
|
G | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1608+552G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86722986 | ||||||
| chr4:86723368
|
C | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1608+934C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86723368 | ||||||
| chr4:86723534
|
C | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1608+1100C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86723534 | ||||||
| chr4:86723535
|
G | A | 1 | a0006c0025t0003g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1608+1101G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86723535 | ||||||
| chr4:86723689
|
G | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1608+1255G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86723689 | ||||||
| chr4:86723958
|
A | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1608+1524A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86723958 | ||||||
| chr4:86724152
|
A | G | 9 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1608+1718A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86724152 | ||||||
| chr4:86724434
|
T | C | 1 | a0007c0007t0004g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1608+2000T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86724434 | ||||||
| chr4:86724476
|
G | A | 2 | a0008c0014t0003g0025a0008c0014t0003g0026 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1608+2042G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86724476 | ||||||
| chr4:86724586
|
C | T | 1 | a0001c0003t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1608+2152C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86724586 | ||||||
| chr4:86724700
|
A | G | 1 | a0002c0001t0002g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1608+2266A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86724700 | ||||||
| chr4:86724769
|
G | A | 1 | a0002c0001t0002g0133 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1608+2335G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86724769 | ||||||
| chr4:86724817
|
C | CT | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1608+2393dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86724817 | |||||
| chr4:86725204
|
A | G | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1608+2770A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86725204 | ||||||
| chr4:86725238
|
TTCATGTC others(5545): Show |
T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1608+2809_1609-160 others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86725238 | |||||
| chr4:86725280
|
A | G | 1 | a0003c0002t0001g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1608+2846A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86725280 | ||||||
| chr4:86725331
|
C | T | 2 | a0003c0002t0001g0091a0003c0002t0001g0190 | 2 | NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1608+2897C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86725331 | ||||||
| chr4:86725345
|
G | A | 1 | a0002c0001t0002g0146 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1608+2911G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86725345 | ||||||
| chr4:86725779
|
G | T | 22 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(19): Show | 22 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1608+3345G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86725779 | ||||||
| chr4:86726110
|
T | C | 7 | a0003c0002t0001g0096a0003c0002t0001g0097a0003c0002t0001g0098others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1608+3676T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86726110 | ||||||
| chr4:86726409
|
C | A | 1 | a0003c0002t0001g0097 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1608+3975C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86726409 | ||||||
| chr4:86726474
|
G | T | 81 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1608+4040G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86726474 | ||||||
| chr4:86726797
|
C | G | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1608+4363C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86726797 | ||||||
| chr4:86726907
|
G | A | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1608+4473G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86726907 | ||||||
| chr4:86726954
|
G | A | 1 | a0002c0001t0002g0147 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1608+4520G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86726954 | ||||||
| chr4:86726970
|
A | G | 4 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(1): Show | 4 | HG02486.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+4536A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86726970 | ||||||
| chr4:86726977
|
A | G | 89 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(86): Show | 89 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1608+4543A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86726977 | ||||||
| chr4:86727060
|
A | T | 1 | a0015c0021t0001g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1608+4626A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86727060 | ||||||
| chr4:86727094
|
T | C | 1 | a0007c0007t0004g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1608+4660T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86727094 | ||||||
| chr4:86727430
|
G | A | 18 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(15): Show | 18 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1609-4970G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86727430 | ||||||
| chr4:86727518
|
G | A | 82 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1609-4882G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86727518 | ||||||
| chr4:86727733
|
C | T | 3 | a0003c0002t0001g0186a0003c0002t0001g0187a0003c0002t0009g0188 | 3 | HG01071.hp1 HG01981.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1609-4667C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86727733 | ||||||
| chr4:86727850
|
T | C | 22 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(19): Show | 22 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1609-4550T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86727850 | ||||||
| chr4:86728020
|
G | A | 1 | a0002c0001t0002g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1609-4380G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86728020 | ||||||
| chr4:86728059
|
C | T | 1 | a0001c0018t0001g0078 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1609-4341C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86728059 | ||||||
| chr4:86728064
|
T | C | 22 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(19): Show | 22 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1609-4336T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86728064 | ||||||
| chr4:86728365
|
A | G | 1 | a0001c0004t0001g0055 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1609-4035A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86728365 | ||||||
| chr4:86728458
|
T | A | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1609-3942T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86728458 | ||||||
| chr4:86728507
|
G | T | 5 | a0003c0006t0001g0030a0003c0006t0010g0029a0008c0014t0003g0025others(2): Show | 5 | HG02717.hp1 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1609-3893G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86728507 | ||||||
| chr4:86728643
|
C | CT | 15 | a0001c0003t0001g0038a0001c0003t0001g0039a0001c0003t0001g0057others(12): Show | 15 | HG01106.hp2 HG01123.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1609-3723dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728643
|
C | CTT | 5 | a0001c0003t0001g0037a0001c0003t0001g0094a0006c0010t0003g0196others(2): Show | 5 | HG02135.hp1 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1609-3724_1609-372 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728643
|
C | CTTT | 24 | a0001c0003t0001g0035a0001c0003t0001g0085a0002c0001t0002g0105others(21): Show | 24 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1609-3725_1609-372 others(7): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728643
|
C | CTTTT | 22 | a0002c0001t0002g0104a0002c0001t0002g0107a0002c0001t0002g0111others(19): Show | 22 | HG00140.hp1 HG00423.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1609-3726_1609-372 others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728643
|
C | CTTTTT | 9 | a0002c0001t0002g0116a0002c0001t0002g0122a0002c0001t0002g0141others(6): Show | 9 | HG00609.hp2 HG01361.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1609-3727_1609-372 others(9): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728643
|
C | CTTTTTT | 5 | a0002c0001t0002g0109a0002c0001t0002g0134a0002c0001t0002g0135others(2): Show | 5 | HG00642.hp2 HG01168.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1609-3728_1609-372 others(10): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728643
|
C | CTTTTTTT others(1): Show |
5 | a0003c0006t0003g0023a0003c0006t0010g0029a0006c0025t0003g0020others(2): Show | 5 | HG02451.hp1 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1609-3730_1609-372 others(12): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728643
|
C | CTTTTTTT others(3): Show |
2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1609-3732_1609-372 others(14): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728643
|
C | CTTTTTTT others(6): Show |
1 | a0003c0002t0002g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1609-3735_1609-372 others(17): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728643
|
C | CTTTTTTT others(10): Show |
1 | a0003c0002t0002g0017 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1609-3739_1609-372 others(21): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728643
|
C | CTTTTTTT others(11): Show |
1 | a0003c0002t0002g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1609-3740_1609-372 others(22): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728643
|
C | CTTTTTTT others(12): Show |
1 | a0003c0002t0002g0016 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1609-3741_1609-372 others(23): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728643
|
CT | C | 42 | a0001c0003t0001g0034a0001c0003t0001g0044a0001c0003t0001g0058others(39): Show | 42 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1609-3723delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728643
|
CTTTTTTT others(6): Show |
C | 1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1609-3735_1609-372 others(17): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728643 | |||||
| chr4:86728655
|
T | A | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609-3745T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86728655 | ||||||
| chr4:86728660
|
T | TTATTTAT others(3): Show |
2 | a0007c0007t0005g0175a0007c0007t0005g0179 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1609-3739_1609-373 others(14): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86728660 | |||||
| chr4:86728661
|
T | TATTTATT others(2): Show |
2 | a0007c0007t0004g0132a0007c0007t0004g0167 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1609-3739_1609-373 others(13): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86728661 | ||||||
| chr4:86728665
|
T | A | 1 | a0007c0007t0004g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1609-3735T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86728665 | ||||||
| chr4:86728767
|
C | T | 1 | a0002c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1609-3633C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86728767 | ||||||
| chr4:86729008
|
C | T | 1 | a0002c0001t0002g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1609-3392C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86729008 | ||||||
| chr4:86729062
|
G | C | 1 | a0002c0001t0002g0157 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1609-3338G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86729062 | ||||||
| chr4:86729451
|
A | C | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1609-2949A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86729451 | ||||||
| chr4:86729459
|
T | C | 13 | a0003c0006t0001g0030a0003c0006t0003g0021a0003c0006t0003g0022others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1609-2941T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86729459 | ||||||
| chr4:86729543
|
T | C | 4 | a0002c0001t0002g0158a0002c0001t0002g0159a0002c0001t0002g0160others(1): Show | 4 | HG00609.hp2 HG02056.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609-2857T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86729543 | ||||||
| chr4:86729657
|
A | G | 7 | a0003c0002t0001g0096a0003c0002t0001g0097a0003c0002t0001g0098others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609-2743A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86729657 | ||||||
| chr4:86729867
|
C | G | 13 | a0003c0006t0001g0030a0003c0006t0003g0021a0003c0006t0003g0022others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1609-2533C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86729867 | ||||||
| chr4:86729908
|
G | C | 4 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(1): Show | 4 | HG02486.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-2492G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86729908 | ||||||
| chr4:86730070
|
A | G | 1 | a0003c0002t0001g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1609-2330A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86730070 | ||||||
| chr4:86730371
|
A | C | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1609-2029A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86730371 | ||||||
| chr4:86730548
|
G | C | 22 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(19): Show | 22 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1609-1852G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86730548 | ||||||
| chr4:86730620
|
G | A | 2 | a0001c0003t0001g0062a0001c0003t0002g0006 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1609-1780G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86730620 | ||||||
| chr4:86730712
|
A | C | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609-1688A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86730712 | ||||||
| chr4:86730807
|
G | T | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1609-1593G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86730807 | ||||||
| chr4:86730874
|
C | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1609-1526C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86730874 | ||||||
| chr4:86730882
|
G | T | 1 | a0003c0002t0002g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1609-1518G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86730882 | ||||||
| chr4:86730887
|
G | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1609-1513G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86730887 | ||||||
| chr4:86730917
|
T | C | 13 | a0003c0006t0001g0030a0003c0006t0003g0021a0003c0006t0003g0022others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1609-1483T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86730917 | ||||||
| chr4:86730964
|
T | A | 1 | a0002c0001t0002g0159 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1609-1436T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86730964 | ||||||
| chr4:86731250
|
A | G | 2 | a0009c0012t0001g0185a0009c0012t0001g0191 | 2 | HG00438.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1609-1150A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86731250 | ||||||
| chr4:86731398
|
C | G | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1609-1002C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86731398 | ||||||
| chr4:86731441
|
CT | C | 5 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(2): Show | 5 | HG01981.hp2 HG02015.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1609-956delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr4 | 86731441 | |||||
| chr4:86731454
|
AATATTTT others(8): Show |
A | 1 | a0003c0002t0002g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1609-945_1609-931d others(17): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86731454 | ||||||
| chr4:86731585
|
C | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1609-815C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86731585 | ||||||
| chr4:86731609
|
T | G | 1 | a0003c0002t0001g0168 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-791T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86731609 | ||||||
| chr4:86731787
|
T | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1609-613T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86731787 | ||||||
| chr4:86731895
|
G | A | 3 | a0002c0001t0002g0147a0002c0001t0002g0154a0002c0001t0002g0155 | 3 | HG00140.hp1 HG00639.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1609-505G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86731895 | ||||||
| chr4:86731943
|
G | A | 1 | a0002c0001t0002g0153 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1609-457G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86731943 | ||||||
| chr4:86732319
|
T | C | 1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1609-81T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 10/47 | chr4 | 86732319 | ||||||
| chr4:86732558
|
T | C | 3 | a0003c0002t0001g0099a0003c0002t0001g0100a0003c0002t0001g0101 | 3 | HG02451.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1684-34T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 11/47 | chr4 | 86732558 | ||||||
| chr4:86732839
|
A | C | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1858+73A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 12/47 | chr4 | 86732839 | ||||||
| chr4:86732979
|
A | T | 1 | a0002c0001t0002g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1858+213A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 12/47 | chr4 | 86732979 | ||||||
| chr4:86733164
|
C | T | 1 | a0003c0002t0005g0169 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1858+398C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 12/47 | chr4 | 86733164 | ||||||
| chr4:86733347
|
A | G | 1 | a0001c0003t0001g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1858+581A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 12/47 | chr4 | 86733347 | ||||||
| chr4:86733558
|
G | A | 3 | a0008c0014t0003g0025a0008c0014t0003g0026a0008c0032t0003g0028 | 3 | HG02717.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1859-745G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 12/47 | chr4 | 86733558 | ||||||
| chr4:86733856
|
CAAT | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1859-438_1859-436d others(5): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr4 | 86733856 | |||||
| chr4:86733900
|
G | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1859-403G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 12/47 | chr4 | 86733900 | ||||||
| chr4:86734545
|
TCA | T | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2012+90_2012+91del others(2): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 13/47 | chr4 | 86734545 | ||||||
| chr4:86734598
|
A | G | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2013-139A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 13/47 | chr4 | 86734598 | ||||||
| chr4:86734600
|
C | T | 32 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(29): Show | 32 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.2013-137C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 13/47 | chr4 | 86734600 | ||||||
| chr4:86734878
|
A | G | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2151+3A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 14/47 | chr4 | 86734878 | ||||||
| chr4:86735006
|
G | A | 32 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(29): Show | 32 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.2151+131G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 14/47 | chr4 | 86735006 | ||||||
| chr4:86735058
|
A | AT | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2151+192dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr4 | 86735058 | |||||
| chr4:86735308
|
A | C | 1 | a0002c0011t0001g0113 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2152-286A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 14/47 | chr4 | 86735308 | ||||||
| chr4:86735429
|
G | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2152-165G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 14/47 | chr4 | 86735429 | ||||||
| chr4:86735839
|
G | A | 28 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(25): Show | 28 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.2304+93G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86735839 | ||||||
| chr4:86736048
|
G | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2304+302G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86736048 | ||||||
| chr4:86736121
|
T | C | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2304+375T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86736121 | ||||||
| chr4:86736259
|
A | G | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2304+513A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86736259 | ||||||
| chr4:86736432
|
T | C | 1 | a0002c0001t0002g0119 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2304+686T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86736432 | ||||||
| chr4:86736534
|
G | A | 1 | a0003c0002t0005g0169 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2304+788G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86736534 | ||||||
| chr4:86736570
|
T | A | 13 | a0003c0006t0001g0030a0003c0006t0003g0021a0003c0006t0003g0022others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2304+824T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86736570 | ||||||
| chr4:86737237
|
C | CAAATA | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2304+1507_2304+151 others(9): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr4 | 86737237 | |||||
| chr4:86737310
|
T | G | 1 | a0008c0032t0003g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2304+1564T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86737310 | ||||||
| chr4:86737550
|
C | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2304+1804C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86737550 | ||||||
| chr4:86737652
|
G | GT | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2304+1917dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr4 | 86737652 | |||||
| chr4:86737889
|
T | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2304+2143T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86737889 | ||||||
| chr4:86737902
|
A | G | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2304+2156A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86737902 | ||||||
| chr4:86738034
|
A | T | 1 | a0003c0002t0009g0188 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2304+2288A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86738034 | ||||||
| chr4:86738054
|
T | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2304+2308T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86738054 | ||||||
| chr4:86738071
|
G | GTAGTTTC others(3): Show |
1 | a0001c0004t0001g0086 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2304+2327_2304+233 others(14): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr4 | 86738071 | |||||
| chr4:86738071
|
G | GTAGTTTC others(4): Show |
6 | a0001c0004t0001g0051a0001c0004t0001g0053a0001c0004t0001g0056others(3): Show | 6 | HG00438.hp1 NA18947.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.2304+2326_2304+233 others(15): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr4 | 86738071 | |||||
| chr4:86738091
|
T | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2304+2345T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86738091 | ||||||
| chr4:86738098
|
G | A | 1 | a0003c0002t0001g0186 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2304+2352G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86738098 | ||||||
| chr4:86738185
|
T | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2304+2439T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86738185 | ||||||
| chr4:86738312
|
G | A | 32 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(29): Show | 32 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.2304+2566G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86738312 | ||||||
| chr4:86739027
|
A | T | 1 | a0001c0004t0001g0070 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2305-2607A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86739027 | ||||||
| chr4:86739048
|
A | G | 1 | a0001c0004t0001g0069 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2305-2586A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86739048 | ||||||
| chr4:86739321
|
C | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2305-2313C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86739321 | ||||||
| chr4:86739477
|
C | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2305-2157C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86739477 | ||||||
| chr4:86739558
|
T | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2305-2076T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86739558 | ||||||
| chr4:86739559
|
T | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2305-2075T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86739559 | ||||||
| chr4:86739577
|
A | C | 1 | a0007c0007t0004g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2305-2057A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86739577 | ||||||
| chr4:86739704
|
G | C | 1 | a0019c0024t0004g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2305-1930G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86739704 | ||||||
| chr4:86739969
|
G | A | 18 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(15): Show | 18 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.2305-1665G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86739969 | ||||||
| chr4:86740105
|
C | G | 2 | a0004c0005t0004g0003a0004c0005t0004g0005 | 2 | HG01123.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.2305-1529C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86740105 | ||||||
| chr4:86740204
|
C | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2305-1430C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86740204 | ||||||
| chr4:86740478
|
G | A | 1 | a0002c0001t0002g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2305-1156G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86740478 | ||||||
| chr4:86740647
|
G | C | 58 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.2305-987G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86740647 | ||||||
| chr4:86740771
|
A | G | 18 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(15): Show | 18 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.2305-863A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86740771 | ||||||
| chr4:86740832
|
A | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2305-802A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86740832 | ||||||
| chr4:86740912
|
C | CA | 11 | a0001c0004t0001g0069a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.2305-712dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr4 | 86740912 | |||||
| chr4:86741216
|
A | G | 2 | a0003c0002t0001g0100a0003c0002t0001g0101 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2305-418A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86741216 | ||||||
| chr4:86741267
|
A | G | 1 | a0004c0005t0004g0002 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2305-367A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86741267 | ||||||
| chr4:86741270
|
G | A | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2305-364G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86741270 | ||||||
| chr4:86741550
|
G | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2305-84G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 15/47 | chr4 | 86741550 | ||||||
| chr4:86742211
|
C | T | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2487+395C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86742211 | ||||||
| chr4:86742221
|
G | A | 1 | a0001c0004t0001g0181 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2487+405G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86742221 | ||||||
| chr4:86742297
|
T | G | 2 | a0003c0002t0002g0015a0003c0002t0002g0016 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2487+481T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86742297 | ||||||
| chr4:86742447
|
T | A | 1 | a0002c0001t0002g0138 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2487+631T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86742447 | ||||||
| chr4:86742826
|
C | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2487+1010C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86742826 | ||||||
| chr4:86743277
|
C | G | 1 | a0022c0031t0003g0027 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2487+1461C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86743277 | ||||||
| chr4:86743339
|
T | C | 1 | a0004c0005t0005g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2487+1523T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86743339 | ||||||
| chr4:86743373
|
T | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2487+1557T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86743373 | ||||||
| chr4:86743381
|
A | G | 1 | a0003c0002t0001g0180 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2487+1565A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86743381 | ||||||
| chr4:86743397
|
CAGTG | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2488-1566_2488-156 others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | INFO_REALIGN_3_PRIME | chr4 | 86743397 | |||||
| chr4:86743477
|
GA | G | 5 | a0001c0004t0001g0087a0007c0007t0004g0132a0007c0007t0004g0167others(2): Show | 5 | HG01106.hp2 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2488-1479delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | INFO_REALIGN_3_PRIME | chr4 | 86743477 | |||||
| chr4:86743701
|
A | G | 32 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(29): Show | 32 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.2488-1265A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86743701 | ||||||
| chr4:86743880
|
C | T | 1 | a0002c0001t0002g0127 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2488-1086C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86743880 | ||||||
| chr4:86744061
|
A | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2488-905A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86744061 | ||||||
| chr4:86744231
|
T | C | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.2488-735T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86744231 | ||||||
| chr4:86744296
|
T | C | 9 | a0004c0005t0004g0002a0004c0005t0004g0003a0004c0005t0004g0004others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2488-670T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86744296 | ||||||
| chr4:86744336
|
A | T | 2 | a0001c0003t0001g0062a0001c0003t0002g0006 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2488-630A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86744336 | ||||||
| chr4:86744571
|
C | T | 1 | a0002c0001t0002g0110 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2488-395C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86744571 | ||||||
| chr4:86744942
|
G | A | 1 | a0006c0010t0003g0196 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2488-24G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 16/47 | chr4 | 86744942 | ||||||
| chr4:86745181
|
G | C | 5 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(2): Show | 5 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+53G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86745181 | ||||||
| chr4:86745442
|
G | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2650+314G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86745442 | ||||||
| chr4:86745530
|
A | G | 32 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(29): Show | 32 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.2650+402A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86745530 | ||||||
| chr4:86745750
|
T | C | 99 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(96): Show | 99 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.2650+622T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86745750 | ||||||
| chr4:86745755
|
G | A | 5 | a0003c0006t0001g0030a0003c0006t0010g0029a0008c0014t0003g0025others(2): Show | 5 | HG02717.hp1 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+627G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86745755 | ||||||
| chr4:86745763
|
G | A | 5 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(2): Show | 5 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+635G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86745763 | ||||||
| chr4:86745826
|
A | C | 1 | a0003c0002t0001g0097 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2650+698A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86745826 | ||||||
| chr4:86745896
|
A | G | 1 | a0003c0009t0001g0102 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2650+768A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86745896 | ||||||
| chr4:86745990
|
G | A | 1 | a0001c0004t0001g0071 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2650+862G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86745990 | ||||||
| chr4:86746007
|
G | T | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2650+879G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86746007 | ||||||
| chr4:86746018
|
G | A | 9 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2650+890G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86746018 | ||||||
| chr4:86746053
|
T | C | 92 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.2650+925T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86746053 | ||||||
| chr4:86746500
|
TA | T | 5 | a0003c0006t0001g0030a0003c0006t0010g0029a0008c0014t0003g0025others(2): Show | 5 | HG02717.hp1 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+1373delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86746500 | ||||||
| chr4:86746550
|
G | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2650+1422G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86746550 | ||||||
| chr4:86746583
|
T | C | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2650+1455T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86746583 | ||||||
| chr4:86746775
|
C | A | 1 | a0007c0007t0004g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2650+1647C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86746775 | ||||||
| chr4:86746865
|
C | T | 1 | a0001c0004t0001g0073 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2650+1737C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86746865 | ||||||
| chr4:86746876
|
C | T | 31 | a0001c0004t0001g0032a0001c0004t0001g0036a0001c0004t0001g0048others(28): Show | 31 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.2650+1748C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86746876 | ||||||
| chr4:86746881
|
C | T | 1 | a0001c0003t0001g0092 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2650+1753C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86746881 | ||||||
| chr4:86747096
|
A | G | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2650+1968A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86747096 | ||||||
| chr4:86747151
|
G | A | 5 | a0001c0003t0001g0035a0001c0003t0001g0037a0001c0003t0001g0038others(2): Show | 5 | NA18951.hp1 NA18953.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+2023G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86747151 | ||||||
| chr4:86747374
|
G | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2650+2246G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86747374 | ||||||
| chr4:86747456
|
A | G | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2650+2328A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86747456 | ||||||
| chr4:86747522
|
A | G | 1 | a0002c0001t0002g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2650+2394A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86747522 | ||||||
| chr4:86747524
|
C | T | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2650+2396C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86747524 | ||||||
| chr4:86747525
|
G | A | 11 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.2650+2397G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86747525 | ||||||
| chr4:86747533
|
TAGC | T | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2650+2418_2650+242 others(7): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | INFO_REALIGN_3_PRIME | chr4 | 86747533 | |||||
| chr4:86747533
|
TAGCAGCA others(17): Show |
T | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+2421_2650+244 others(28): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | INFO_REALIGN_3_PRIME | chr4 | 86747533 | |||||
| chr4:86747534
|
AGCAGCAG others(8): Show |
A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2650+2421_2650+243 others(19): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | INFO_REALIGN_3_PRIME | chr4 | 86747534 | |||||
| chr4:86747549
|
GGCAGCAG others(5): Show |
G | 3 | a0006c0010t0003g0194a0006c0010t0003g0195a0006c0010t0003g0196 | 3 | HG02486.hp1 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2650+2444_2650+245 others(16): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | INFO_REALIGN_3_PRIME | chr4 | 86747549 | |||||
| chr4:86747549
|
GGCAGCAG others(8): Show |
G | 1 | a0018c0023t0002g0143 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2650+2441_2650+245 others(19): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | INFO_REALIGN_3_PRIME | chr4 | 86747549 | |||||
| chr4:86747552
|
A | G | 1 | a0001c0003t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2650+2424A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86747552 | ||||||
| chr4:86747581
|
C | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2650+2453C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86747581 | ||||||
| chr4:86747584
|
T | C | 11 | a0001c0003t0001g0081a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.2650+2456T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86747584 | ||||||
| chr4:86747774
|
T | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2650+2646T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86747774 | ||||||
| chr4:86747887
|
G | A | 3 | a0002c0001t0002g0104a0002c0001t0002g0156a0002c0001t0002g0157 | 3 | HG04115.hp2 NA18968.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.2651-2583G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86747887 | ||||||
| chr4:86748026
|
A | G | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2651-2444A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86748026 | ||||||
| chr4:86748106
|
A | C | 1 | a0014c0026t0003g0019 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2651-2364A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86748106 | ||||||
| chr4:86748524
|
C | T | 32 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(29): Show | 32 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.2651-1946C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86748524 | ||||||
| chr4:86748665
|
T | A | 1 | a0003c0002t0001g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2651-1805T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86748665 | ||||||
| chr4:86748671
|
T | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2651-1799T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86748671 | ||||||
| chr4:86748675
|
T | G | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2651-1795T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86748675 | ||||||
| chr4:86748687
|
G | A | 1 | a0001c0003t0001g0059 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2651-1783G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86748687 | ||||||
| chr4:86748716
|
C | T | 13 | a0003c0006t0001g0030a0003c0006t0003g0021a0003c0006t0003g0022others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2651-1754C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86748716 | ||||||
| chr4:86748768
|
G | T | 1 | a0001c0003t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2651-1702G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86748768 | ||||||
| chr4:86748884
|
T | C | 11 | a0003c0006t0001g0030a0003c0006t0003g0021a0003c0006t0003g0022others(8): Show | 11 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2651-1586T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86748884 | ||||||
| chr4:86748984
|
T | C | 1 | a0001c0017t0001g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2651-1486T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86748984 | ||||||
| chr4:86749048
|
A | C | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.2651-1422A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86749048 | ||||||
| chr4:86749063
|
C | G | 1 | a0019c0024t0004g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2651-1407C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86749063 | ||||||
| chr4:86749075
|
G | A | 32 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(29): Show | 32 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.2651-1395G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86749075 | ||||||
| chr4:86749149
|
C | T | 1 | a0011c0015t0001g0041 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2651-1321C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86749149 | ||||||
| chr4:86749209
|
A | G | 2 | a0002c0001t0002g0110a0002c0001t0002g0123 | 2 | NA19057.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.2651-1261A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86749209 | ||||||
| chr4:86749254
|
C | T | 14 | a0003c0002t0001g0091a0003c0002t0001g0180a0003c0002t0001g0183others(11): Show | 14 | HG00438.hp2 HG01071.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2651-1216C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86749254 | ||||||
| chr4:86749642
|
A | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2651-828A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86749642 | ||||||
| chr4:86749996
|
C | T | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2651-474C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 17/47 | chr4 | 86749996 | ||||||
| chr4:86750955
|
A | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.3068+68A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 18/47 | chr4 | 86750955 | ||||||
| chr4:86751218
|
C | T | 1 | a0003c0002t0001g0189 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3166+94C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86751218 | ||||||
| chr4:86751575
|
C | T | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3166+451C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86751575 | ||||||
| chr4:86751652
|
A | G | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3166+528A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86751652 | ||||||
| chr4:86751816
|
ATTTTATG others(28): Show |
A | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3166+698_3166+732d others(37): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr4 | 86751816 | |||||
| chr4:86751923
|
A | ATG | 63 | a0001c0003t0001g0038a0001c0004t0001g0181a0002c0001t0002g0104others(60): Show | 63 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.3166+820_3166+821d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr4 | 86751923 | |||||
| chr4:86751923
|
A | ATGTG | 10 | a0002c0001t0002g0121a0004c0005t0004g0001a0004c0005t0004g0002others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.3166+818_3166+821d others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr4 | 86751923 | |||||
| chr4:86752068
|
C | T | 68 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(65): Show | 68 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.3167-941C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86752068 | ||||||
| chr4:86752126
|
A | G | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3167-883A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86752126 | ||||||
| chr4:86752237
|
T | G | 2 | a0002c0001t0002g0134a0002c0001t0002g0135 | 2 | NA18948.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.3167-772T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86752237 | ||||||
| chr4:86752292
|
G | A | 58 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.3167-717G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86752292 | ||||||
| chr4:86752399
|
A | C | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3167-610A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86752399 | ||||||
| chr4:86752550
|
T | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.3167-459T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86752550 | ||||||
| chr4:86752599
|
C | G | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.3167-410C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86752599 | ||||||
| chr4:86752611
|
G | A | 58 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.3167-398G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86752611 | ||||||
| chr4:86752713
|
T | C | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3167-296T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86752713 | ||||||
| chr4:86752737
|
T | C | 18 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(15): Show | 18 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.3167-272T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86752737 | ||||||
| chr4:86752747
|
T | G | 3 | a0003c0002t0001g0096a0003c0002t0001g0098a0003c0002t0001g0103 | 3 | HG02145.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3167-262T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 19/47 | chr4 | 86752747 | ||||||
| chr4:86753081
|
G | C | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3223+16G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86753081 | ||||||
| chr4:86753188
|
T | C | 1 | a0004c0005t0004g0002 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3223+123T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86753188 | ||||||
| chr4:86753307
|
T | G | 1 | a0004c0028t0005g0077 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3223+242T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86753307 | ||||||
| chr4:86753365
|
G | A | 68 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(65): Show | 68 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.3223+300G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86753365 | ||||||
| chr4:86753731
|
A | G | 1 | a0001c0004t0001g0181 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3223+666A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86753731 | ||||||
| chr4:86754223
|
G | A | 7 | a0003c0002t0001g0096a0003c0002t0001g0097a0003c0002t0001g0098others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.3223+1158G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86754223 | ||||||
| chr4:86754224
|
C | T | 1 | a0001c0004t0001g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3223+1159C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86754224 | ||||||
| chr4:86754527
|
G | A | 1 | a0002c0001t0002g0117 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3223+1462G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86754527 | ||||||
| chr4:86754605
|
T | C | 69 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(66): Show | 69 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.3223+1540T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86754605 | ||||||
| chr4:86754897
|
G | A | 1 | a0001c0004t0001g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3223+1832G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86754897 | ||||||
| chr4:86755196
|
G | A | 1 | a0001c0017t0001g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3223+2131G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86755196 | ||||||
| chr4:86755359
|
T | TA | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3223+2305dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr4 | 86755359 | |||||
| chr4:86755359
|
T | TAA | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.3223+2304_3223+230 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr4 | 86755359 | |||||
| chr4:86755412
|
TA | T | 91 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.3223+2352delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr4 | 86755412 | |||||
| chr4:86755642
|
T | C | 9 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.3223+2577T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86755642 | ||||||
| chr4:86755859
|
T | G | 11 | a0003c0006t0001g0030a0003c0006t0003g0021a0003c0006t0003g0022others(8): Show | 11 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3224-2401T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86755859 | ||||||
| chr4:86756096
|
C | T | 1 | a0003c0009t0002g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3224-2164C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86756096 | ||||||
| chr4:86756104
|
T | G | 69 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(66): Show | 69 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.3224-2156T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86756104 | ||||||
| chr4:86756200
|
T | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.3224-2060T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86756200 | ||||||
| chr4:86756244
|
G | T | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3224-2016G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86756244 | ||||||
| chr4:86757090
|
G | A | 9 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.3224-1170G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86757090 | ||||||
| chr4:86757142
|
CAT | C | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3224-1115_3224-111 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr4 | 86757142 | |||||
| chr4:86757273
|
G | T | 92 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.3224-987G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86757273 | ||||||
| chr4:86757285
|
G | A | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3224-975G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86757285 | ||||||
| chr4:86757374
|
T | C | 69 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(66): Show | 69 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.3224-886T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86757374 | ||||||
| chr4:86757634
|
C | T | 58 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.3224-626C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86757634 | ||||||
| chr4:86757762
|
C | CAAAAAAA others(6): Show |
7 | a0004c0005t0004g0001a0004c0005t0004g0003a0004c0005t0004g0004others(4): Show | 7 | HG00738.hp2 HG01099.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.3224-494_3224-482d others(15): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr4 | 86757762 | |||||
| chr4:86757762
|
C | CAAAAAAA others(7): Show |
1 | a0004c0005t0004g0005 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3224-495_3224-482d others(16): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr4 | 86757762 | |||||
| chr4:86757762
|
C | CAAAAAAA others(8): Show |
2 | a0004c0005t0004g0002a0012c0016t0006g0198 | 2 | HG01346.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3224-496_3224-482d others(17): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr4 | 86757762 | |||||
| chr4:86757762
|
C | CAAAAAAA others(12): Show |
1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3224-482_3224-481i others(21): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr4 | 86757762 | |||||
| chr4:86757762
|
C | CAAAAAAA others(13): Show |
5 | a0003c0002t0002g0014a0003c0002t0002g0016a0003c0002t0002g0017others(2): Show | 5 | HG02615.hp2 HG03041.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3224-482_3224-481i others(22): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr4 | 86757762 | |||||
| chr4:86757762
|
C | CAAAAAAA others(14): Show |
2 | a0003c0002t0002g0015a0010c0013t0003g0011 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3224-482_3224-481i others(23): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr4 | 86757762 | |||||
| chr4:86757762
|
C | CAAAAAAA others(15): Show |
3 | a0003c0006t0003g0021a0003c0006t0003g0023a0006c0025t0003g0020 | 3 | HG02451.hp1 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3224-482_3224-481i others(24): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr4 | 86757762 | |||||
| chr4:86757762
|
C | CAAAAAAA others(16): Show |
3 | a0003c0006t0003g0022a0003c0006t0003g0024a0014c0026t0003g0019 | 3 | HG01891.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3224-482_3224-481i others(25): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr4 | 86757762 | |||||
| chr4:86758151
|
G | C | 1 | a0002c0001t0002g0116 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3224-109G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86758151 | ||||||
| chr4:86758219
|
G | A | 1 | a0001c0004t0008g0049 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3224-41G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 20/47 | chr4 | 86758219 | ||||||
| chr4:86758360
|
G | C | 14 | a0003c0002t0001g0091a0003c0002t0001g0180a0003c0002t0001g0183others(11): Show | 14 | HG00438.hp2 HG01071.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.3313+11G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 21/47 | chr4 | 86758360 | ||||||
| chr4:86758410
|
T | C | 1 | a0003c0002t0001g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3313+61T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 21/47 | chr4 | 86758410 | ||||||
| chr4:86758489
|
A | C | 154 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0058others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.3313+140A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 21/47 | chr4 | 86758489 | ||||||
| chr4:86759084
|
T | C | 1 | a0004c0005t0004g0001 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3553+11T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86759084 | ||||||
| chr4:86759522
|
G | C | 1 | a0008c0032t0003g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3553+449G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86759522 | ||||||
| chr4:86759635
|
C | T | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3553+562C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86759635 | ||||||
| chr4:86760204
|
A | G | 1 | a0003c0002t0001g0172 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3553+1131A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86760204 | ||||||
| chr4:86760715
|
G | C | 1 | a0001c0003t0001g0092 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3553+1642G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86760715 | ||||||
| chr4:86760718
|
T | C | 1 | a0001c0027t0001g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3553+1645T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86760718 | ||||||
| chr4:86761136
|
G | A | 1 | a0003c0002t0001g0172 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3554-1591G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86761136 | ||||||
| chr4:86761139
|
A | AAT | 32 | a0001c0003t0001g0035a0001c0003t0001g0037a0001c0003t0001g0038others(29): Show | 32 | HG01071.hp1 HG01081.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.3554-1558_3554-155 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761139
|
A | AATAT | 10 | a0001c0003t0001g0079a0001c0003t0001g0080a0001c0003t0001g0081others(7): Show | 10 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.3554-1560_3554-155 others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761139
|
A | AATATAT | 23 | a0001c0003t0001g0062a0001c0003t0002g0006a0001c0004t0001g0073others(20): Show | 23 | HG00738.hp2 HG01099.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.3554-1562_3554-155 others(10): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761139
|
A | AATATATA others(1): Show |
25 | a0001c0003t0001g0033a0001c0003t0001g0057a0001c0003t0001g0058others(22): Show | 25 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.3554-1564_3554-155 others(12): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761139
|
A | AATATATA others(3): Show |
22 | a0001c0003t0001g0063a0002c0001t0002g0110a0002c0001t0002g0131others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.3554-1566_3554-155 others(14): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761139
|
A | AATATATA others(5): Show |
24 | a0001c0003t0001g0034a0001c0003t0001g0060a0001c0003t0001g0064others(21): Show | 24 | HG00423.hp1 HG00642.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.3554-1568_3554-155 others(16): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761139
|
A | AATATATA others(7): Show |
5 | a0001c0003t0001g0059a0002c0001t0002g0141a0002c0001t0002g0142others(2): Show | 5 | HG01361.hp1 HG03516.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.3554-1570_3554-155 others(18): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761139
|
A | AATATATA others(9): Show |
3 | a0002c0001t0002g0116a0003c0006t0001g0030a0008c0014t0003g0025 | 3 | HG01496.hp2 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3554-1572_3554-155 others(20): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761139
|
A | AATATATA others(11): Show |
4 | a0002c0001t0002g0115a0002c0001t0002g0148a0003c0002t0002g0015others(1): Show | 4 | HG02273.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3554-1574_3554-155 others(22): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761139
|
A | AATATATA others(13): Show |
1 | a0002c0001t0002g0153 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3554-1576_3554-155 others(24): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761139
|
A | AATATATA others(15): Show |
1 | a0001c0003t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3554-1578_3554-155 others(26): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761139
|
A | ATATATAT others(8): Show |
1 | a0002c0001t0002g0160 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3554-1588_3554-158 others(19): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86761139 | ||||||
| chr4:86761139
|
AAT | A | 6 | a0001c0004t0001g0052a0001c0004t0001g0053a0001c0004t0001g0086others(3): Show | 6 | HG01243.hp2 NA18947.hp1 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.3554-1558_3554-155 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761139
|
AATAT | A | 7 | a0001c0004t0008g0049a0003c0002t0001g0096a0003c0002t0001g0097others(4): Show | 7 | HG00642.hp1 HG01099.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.3554-1560_3554-155 others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761139
|
AATATATA others(7): Show |
A | 1 | a0002c0001t0002g0117 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3554-1570_3554-155 others(18): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86761139 | |||||
| chr4:86761171
|
A | T | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3554-1556A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86761171 | ||||||
| chr4:86761265
|
A | G | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.3554-1462A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86761265 | ||||||
| chr4:86761616
|
A | G | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3554-1111A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86761616 | ||||||
| chr4:86762006
|
C | T | 22 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(19): Show | 22 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.3554-721C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86762006 | ||||||
| chr4:86762098
|
G | A | 1 | a0003c0002t0001g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3554-629G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86762098 | ||||||
| chr4:86762165
|
G | T | 1 | a0003c0006t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3554-562G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86762165 | ||||||
| chr4:86762398
|
CTATT | C | 4 | a0003c0002t0001g0168a0003c0002t0001g0171a0003c0002t0001g0172others(1): Show | 4 | HG01243.hp2 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.3554-326_3554-323d others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr4 | 86762398 | |||||
| chr4:86762647
|
A | T | 1 | a0001c0018t0001g0078 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3554-80A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86762647 | ||||||
| chr4:86762680
|
C | T | 1 | a0007c0007t0005g0175 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3554-47C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 23/47 | chr4 | 86762680 | ||||||
| chr4:86763297
|
A | G | 2 | a0008c0014t0003g0025a0008c0014t0003g0026 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4017+107A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 24/47 | chr4 | 86763297 | ||||||
| chr4:86765009
|
T | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.4149+285T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 25/47 | chr4 | 86765009 | ||||||
| chr4:86765026
|
C | T | 18 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(15): Show | 18 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.4149+302C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 25/47 | chr4 | 86765026 | ||||||
| chr4:86765106
|
A | G | 1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4150-289A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 25/47 | chr4 | 86765106 | ||||||
| chr4:86765184
|
A | T | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4150-211A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 25/47 | chr4 | 86765184 | ||||||
| chr4:86765833
|
GT | G | 6 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.4243+356delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr4 | 86765833 | |||||
| chr4:86765846
|
G | T | 1 | a0001c0003t0001g0068 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4243+358G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 26/47 | chr4 | 86765846 | ||||||
| chr4:86766047
|
C | T | 1 | a0003c0002t0005g0169 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4244-385C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 26/47 | chr4 | 86766047 | ||||||
| chr4:86766110
|
G | A | 1 | a0002c0001t0002g0133 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.4244-322G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 26/47 | chr4 | 86766110 | ||||||
| chr4:86766142
|
T | C | 72 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.4244-290T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 26/47 | chr4 | 86766142 | ||||||
| chr4:86766378
|
A | G | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.4244-54A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 26/47 | chr4 | 86766378 | ||||||
| chr4:86766561
|
C | G | 1 | a0002c0001t0002g0110 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4329+44C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 27/47 | chr4 | 86766561 | ||||||
| chr4:86766592
|
T | C | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4329+75T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 27/47 | chr4 | 86766592 | ||||||
| chr4:86766845
|
T | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.4329+328T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 27/47 | chr4 | 86766845 | ||||||
| chr4:86766980
|
C | T | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.4329+463C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 27/47 | chr4 | 86766980 | ||||||
| chr4:86767157
|
C | T | 4 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4329+640C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 27/47 | chr4 | 86767157 | ||||||
| chr4:86767242
|
C | CT | 21 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(18): Show | 21 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.4330-559dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr4 | 86767242 | |||||
| chr4:86767242
|
C | CTT | 11 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.4330-560_4330-559d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr4 | 86767242 | |||||
| chr4:86767275
|
C | T | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.4330-542C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 27/47 | chr4 | 86767275 | ||||||
| chr4:86767371
|
A | G | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.4330-446A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 27/47 | chr4 | 86767371 | ||||||
| chr4:86767399
|
C | T | 1 | a0008c0032t0003g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4330-418C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 27/47 | chr4 | 86767399 | ||||||
| chr4:86767691
|
A | C | 1 | a0001c0003t0001g0093 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4330-126A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 27/47 | chr4 | 86767691 | ||||||
| chr4:86768115
|
A | G | 33 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(30): Show | 33 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.4489+139A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 28/47 | chr4 | 86768115 | ||||||
| chr4:86768247
|
G | C | 1 | a0003c0002t0002g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4489+271G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 28/47 | chr4 | 86768247 | ||||||
| chr4:86768298
|
G | T | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.4489+322G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 28/47 | chr4 | 86768298 | ||||||
| chr4:86768380
|
A | G | 27 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(24): Show | 27 | HG00738.hp2 HG01099.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.4489+404A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 28/47 | chr4 | 86768380 | ||||||
| chr4:86768608
|
T | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.4489+632T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 28/47 | chr4 | 86768608 | ||||||
| chr4:86768679
|
A | T | 1 | a0001c0004t0001g0181 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4489+703A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 28/47 | chr4 | 86768679 | ||||||
| chr4:86768708
|
TC | T | 4 | a0007c0007t0004g0167a0007c0007t0005g0175a0007c0007t0005g0179others(1): Show | 4 | HG02280.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4489+733delC | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 28/47 | chr4 | 86768708 | ||||||
| chr4:86768709
|
C | CT | 13 | a0001c0003t0001g0061a0002c0001t0002g0140a0003c0006t0003g0021others(10): Show | 13 | HG01175.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.4489+752dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr4 | 86768709 | |||||
| chr4:86768775
|
A | G | 7 | a0003c0002t0001g0096a0003c0002t0001g0097a0003c0002t0001g0098others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.4489+799A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 28/47 | chr4 | 86768775 | ||||||
| chr4:86769257
|
G | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.4490-512G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 28/47 | chr4 | 86769257 | ||||||
| chr4:86769594
|
A | G | 1 | a0003c0009t0001g0102 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.4490-175A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 28/47 | chr4 | 86769594 | ||||||
| chr4:86769688
|
A | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4490-81A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 28/47 | chr4 | 86769688 | ||||||
| chr4:86770623
|
C | G | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.4803+424C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 30/47 | chr4 | 86770623 | ||||||
| chr4:86770785
|
A | G | 1 | a0001c0018t0001g0078 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4804-386A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 30/47 | chr4 | 86770785 | ||||||
| chr4:86770963
|
A | C | 1 | a0003c0002t0001g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4804-208A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 30/47 | chr4 | 86770963 | ||||||
| chr4:86770976
|
T | G | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.4804-195T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 30/47 | chr4 | 86770976 | ||||||
| chr4:86771865
|
G | A | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.5168+330G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 31/47 | chr4 | 86771865 | ||||||
| chr4:86771888
|
A | G | 2 | a0003c0002t0001g0091a0003c0002t0001g0190 | 2 | NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.5168+353A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 31/47 | chr4 | 86771888 | ||||||
| chr4:86772007
|
C | T | 1 | a0001c0003t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.5168+472C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 31/47 | chr4 | 86772007 | ||||||
| chr4:86772036
|
C | G | 1 | a0001c0004t0001g0073 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.5168+501C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 31/47 | chr4 | 86772036 | ||||||
| chr4:86772125
|
T | G | 1 | a0003c0002t0001g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5168+590T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 31/47 | chr4 | 86772125 | ||||||
| chr4:86772242
|
A | G | 15 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.5169-536A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 31/47 | chr4 | 86772242 | ||||||
| chr4:86772303
|
C | T | 2 | a0002c0001t0002g0158a0002c0001t0002g0164 | 2 | HG00609.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.5169-475C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 31/47 | chr4 | 86772303 | ||||||
| chr4:86772493
|
G | A | 1 | a0001c0003t0001g0060 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5169-285G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 31/47 | chr4 | 86772493 | ||||||
| chr4:86772543
|
G | A | 5 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.5169-235G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 31/47 | chr4 | 86772543 | ||||||
| chr4:86773292
|
T | C | 1 | a0001c0003t0001g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.5349+334T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 32/47 | chr4 | 86773292 | ||||||
| chr4:86773408
|
AT | A | 11 | a0003c0002t0001g0168a0003c0002t0001g0171a0003c0002t0001g0172others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.5349+460delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr4 | 86773408 | |||||
| chr4:86773472
|
A | G | 4 | a0003c0002t0001g0168a0003c0002t0001g0171a0003c0002t0001g0172others(1): Show | 4 | HG01243.hp2 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.5349+514A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 32/47 | chr4 | 86773472 | ||||||
| chr4:86773694
|
C | CT | 15 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.5350-669dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr4 | 86773694 | |||||
| chr4:86773865
|
A | G | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5350-508A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 32/47 | chr4 | 86773865 | ||||||
| chr4:86773876
|
A | G | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.5350-497A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 32/47 | chr4 | 86773876 | ||||||
| chr4:86774302
|
G | A | 31 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(28): Show | 31 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.5350-71G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 32/47 | chr4 | 86774302 | ||||||
| chr4:86774328
|
G | T | 9 | a0003c0006t0001g0030a0003c0006t0003g0021a0003c0006t0003g0022others(6): Show | 9 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.5350-45G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 32/47 | chr4 | 86774328 | ||||||
| chr4:86774701
|
T | TTA | 8 | a0001c0003t0001g0035a0001c0003t0001g0037a0001c0003t0001g0038others(5): Show | 8 | NA18943.hp2 NA18951.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.5508+190_5508+191d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr4 | 86774701 | |||||
| chr4:86774701
|
TTA | T | 31 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(28): Show | 31 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.5508+190_5508+191d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr4 | 86774701 | |||||
| chr4:86774705
|
A | T | 4 | a0003c0006t0001g0030a0003c0006t0010g0029a0008c0014t0003g0025others(1): Show | 4 | HG02717.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.5508+174A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 33/47 | chr4 | 86774705 | ||||||
| chr4:86774719
|
A | T | 14 | a0003c0002t0002g0015a0003c0002t0002g0016a0004c0005t0004g0009others(11): Show | 14 | HG00738.hp2 HG01099.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.5508+188A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 33/47 | chr4 | 86774719 | ||||||
| chr4:86774721
|
A | T | 29 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(26): Show | 29 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.5508+190A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 33/47 | chr4 | 86774721 | ||||||
| chr4:86774723
|
T | A | 9 | a0001c0003t0001g0062a0001c0003t0002g0006a0001c0004t0001g0069others(6): Show | 9 | HG02559.hp2 NA18522.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.5508+192T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 33/47 | chr4 | 86774723 | ||||||
| chr4:86774948
|
A | T | 1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5509-223A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 33/47 | chr4 | 86774948 | ||||||
| chr4:86775830
|
A | G | 1 | a0005c0008t0002g0128 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.5891+178A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86775830 | ||||||
| chr4:86775954
|
C | G | 80 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(77): Show | 80 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.5891+302C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86775954 | ||||||
| chr4:86776032
|
G | A | 1 | a0001c0018t0001g0078 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.5891+380G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86776032 | ||||||
| chr4:86776346
|
T | C | 2 | a0002c0001t0002g0120a0002c0001t0002g0163 | 2 | NA18947.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.5891+694T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86776346 | ||||||
| chr4:86776460
|
A | G | 15 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.5891+808A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86776460 | ||||||
| chr4:86776666
|
C | A | 5 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.5891+1014C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86776666 | ||||||
| chr4:86776710
|
A | G | 15 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.5891+1058A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86776710 | ||||||
| chr4:86776893
|
G | A | 15 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.5891+1241G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86776893 | ||||||
| chr4:86777618
|
T | TC | 56 | a0002c0001t0002g0105a0002c0001t0002g0106a0002c0001t0002g0107others(53): Show | 56 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.5891+1968dupC | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr4 | 86777618 | |||||
| chr4:86777786
|
G | A | 5 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5891+2134G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86777786 | ||||||
| chr4:86777940
|
CT | C | 10 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.5891+2291delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr4 | 86777940 | |||||
| chr4:86777945
|
G | C | 5 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5891+2293G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86777945 | ||||||
| chr4:86778331
|
A | G | 4 | a0007c0007t0004g0167a0007c0007t0005g0175a0007c0007t0005g0179others(1): Show | 4 | HG02280.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.5892-2071A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86778331 | ||||||
| chr4:86778479
|
C | CT | 95 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(92): Show | 95 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.5892-1923_5892-192 others(5): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86778479 | ||||||
| chr4:86778482
|
G | GA | 95 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(92): Show | 95 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.5892-1920_5892-191 others(5): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86778482 | ||||||
| chr4:86778512
|
A | G | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.5892-1890A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86778512 | ||||||
| chr4:86778722
|
C | G | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.5892-1680C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86778722 | ||||||
| chr4:86778762
|
T | G | 1 | a0001c0003t0001g0083 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5892-1640T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86778762 | ||||||
| chr4:86778870
|
G | A | 1 | a0001c0004t0001g0051 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.5892-1532G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86778870 | ||||||
| chr4:86778898
|
AT | A | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.5892-1495delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr4 | 86778898 | |||||
| chr4:86778931
|
GA | G | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.5892-1461delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr4 | 86778931 | |||||
| chr4:86779063
|
TA | T | 7 | a0001c0003t0001g0044a0001c0003t0001g0060a0001c0003t0001g0093others(4): Show | 7 | HG01081.hp2 HG01099.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.5892-1322delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr4 | 86779063 | |||||
| chr4:86779231
|
C | T | 4 | a0007c0007t0004g0167a0007c0007t0005g0175a0007c0007t0005g0179others(1): Show | 4 | HG02280.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.5892-1171C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86779231 | ||||||
| chr4:86779232
|
G | A | 1 | a0001c0004t0001g0069 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.5892-1170G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86779232 | ||||||
| chr4:86779290
|
G | A | 9 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(6): Show | 9 | HG01891.hp1 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.5892-1112G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86779290 | ||||||
| chr4:86779310
|
G | A | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.5892-1092G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86779310 | ||||||
| chr4:86779410
|
C | A | 58 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.5892-992C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86779410 | ||||||
| chr4:86779417
|
C | CA | 22 | a0001c0003t0001g0065a0002c0001t0002g0123a0002c0001t0002g0158others(19): Show | 22 | HG00609.hp2 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.5892-969dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr4 | 86779417 | |||||
| chr4:86779661
|
G | A | 5 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5892-741G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86779661 | ||||||
| chr4:86780083
|
T | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.5892-319T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86780083 | ||||||
| chr4:86780325
|
A | G | 1 | a0001c0004t0001g0069 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.5892-77A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86780325 | ||||||
| chr4:86780364
|
T | TG | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.5892-38_5892-37ins others(1): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 35/47 | chr4 | 86780364 | ||||||
| chr4:86780554
|
C | T | 1 | a0009c0012t0001g0191 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5962+82C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86780554 | ||||||
| chr4:86780633
|
G | A | 5 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5962+161G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86780633 | ||||||
| chr4:86780649
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.5962+177A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86780649 | ||||||
| chr4:86780867
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.5962+395G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86780867 | ||||||
| chr4:86780956
|
C | CAG | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.5962+484_5962+485i others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86780956 | ||||||
| chr4:86780956
|
C | T | 1 | a0008c0032t0003g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5962+484C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86780956 | ||||||
| chr4:86781275
|
G | C | 22 | a0001c0003t0001g0035a0001c0003t0001g0037a0001c0003t0001g0038others(19): Show | 22 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.5962+803G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86781275 | ||||||
| chr4:86781302
|
AT | A | 58 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.5962+835delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr4 | 86781302 | |||||
| chr4:86781319
|
G | A | 5 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5962+847G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86781319 | ||||||
| chr4:86781386
|
T | A | 1 | a0003c0002t0001g0189 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.5963-815T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86781386 | ||||||
| chr4:86781465
|
G | A | 4 | a0005c0008t0002g0128a0005c0008t0002g0150a0005c0008t0002g0152others(1): Show | 4 | NA19007.hp2 NA19058.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.5963-736G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86781465 | ||||||
| chr4:86781609
|
G | A | 2 | a0001c0003t0001g0061a0006c0010t0003g0194 | 2 | HG01175.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5963-592G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86781609 | ||||||
| chr4:86781723
|
GCGAGGC | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.5963-471_5963-466d others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr4 | 86781723 | |||||
| chr4:86781792
|
G | A | 5 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5963-409G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86781792 | ||||||
| chr4:86781808
|
T | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.5963-393T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86781808 | ||||||
| chr4:86781831
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.5963-370C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86781831 | ||||||
| chr4:86781832
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.5963-369A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86781832 | ||||||
| chr4:86781843
|
A | G | 7 | a0003c0002t0001g0096a0003c0002t0001g0097a0003c0002t0001g0098others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.5963-358A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86781843 | ||||||
| chr4:86781856
|
G | A | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.5963-345G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86781856 | ||||||
| chr4:86781918
|
G | A | 24 | a0002c0001t0002g0105a0002c0001t0002g0107a0002c0001t0002g0108others(21): Show | 24 | HG00423.hp1 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.5963-283G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86781918 | ||||||
| chr4:86781960
|
G | GA | 5 | a0001c0003t0001g0061a0003c0002t0003g0193a0008c0014t0003g0025others(2): Show | 5 | HG00642.hp2 HG01175.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.5963-227dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr4 | 86781960 | |||||
| chr4:86781989
|
C | G | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.5963-212C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86781989 | ||||||
| chr4:86782015
|
T | C | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.5963-186T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86782015 | ||||||
| chr4:86782089
|
G | A | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.5963-112G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86782089 | ||||||
| chr4:86782147
|
C | T | 1 | a0001c0003t0001g0059 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.5963-54C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86782147 | ||||||
| chr4:86782164
|
T | C | 1 | a0003c0002t0001g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5963-37T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 36/47 | chr4 | 86782164 | ||||||
| chr4:86782277
|
A | C | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.6024+15A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86782277 | ||||||
| chr4:86782414
|
C | T | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.6024+152C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86782414 | ||||||
| chr4:86782711
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6024+449G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86782711 | ||||||
| chr4:86782815
|
A | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6024+553A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86782815 | ||||||
| chr4:86782990
|
T | C | 1 | a0002c0001t0002g0153 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.6024+728T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86782990 | ||||||
| chr4:86783010
|
A | G | 1 | a0001c0004t0001g0181 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.6024+748A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86783010 | ||||||
| chr4:86783061
|
A | T | 5 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.6024+799A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86783061 | ||||||
| chr4:86783129
|
G | C | 1 | a0001c0003t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6024+867G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86783129 | ||||||
| chr4:86783564
|
TC | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6025-899delC | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | INFO_REALIGN_3_PRIME | chr4 | 86783564 | |||||
| chr4:86783570
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6025-895A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86783570 | ||||||
| chr4:86783637
|
A | G | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.6025-828A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86783637 | ||||||
| chr4:86783675
|
G | A | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.6025-790G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86783675 | ||||||
| chr4:86783816
|
A | C | 60 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.6025-649A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86783816 | ||||||
| chr4:86784132
|
C | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6025-333C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86784132 | ||||||
| chr4:86784237
|
G | A | 2 | a0008c0014t0003g0025a0008c0014t0003g0026 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.6025-228G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86784237 | ||||||
| chr4:86784325
|
T | C | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.6025-140T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 37/47 | chr4 | 86784325 | ||||||
| chr4:86784635
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6118+77C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 38/47 | chr4 | 86784635 | ||||||
| chr4:86784651
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6118+93A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 38/47 | chr4 | 86784651 | ||||||
| chr4:86784672
|
G | T | 1 | a0003c0002t0002g0184 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.6118+114G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 38/47 | chr4 | 86784672 | ||||||
| chr4:86784709
|
T | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6118+151T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 38/47 | chr4 | 86784709 | ||||||
| chr4:86784968
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6119-263G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 38/47 | chr4 | 86784968 | ||||||
| chr4:86785035
|
A | G | 1 | a0003c0002t0005g0169 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.6119-196A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 38/47 | chr4 | 86785035 | ||||||
| chr4:86785379
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6256+11C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 39/47 | chr4 | 86785379 | ||||||
| chr4:86785464
|
T | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6256+96T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 39/47 | chr4 | 86785464 | ||||||
| chr4:86785503
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6256+135C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 39/47 | chr4 | 86785503 | ||||||
| chr4:86785521
|
A | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6256+153A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 39/47 | chr4 | 86785521 | ||||||
| chr4:86785537
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6256+169A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 39/47 | chr4 | 86785537 | ||||||
| chr4:86785671
|
C | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6257-177C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 39/47 | chr4 | 86785671 | ||||||
| chr4:86786060
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+124C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86786060 | ||||||
| chr4:86786061
|
G | A | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.6345+125G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86786061 | ||||||
| chr4:86786326
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+390C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86786326 | ||||||
| chr4:86786346
|
C | T | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.6345+410C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86786346 | ||||||
| chr4:86786399
|
CTG | C | 24 | a0002c0001t0002g0105a0002c0001t0002g0107a0002c0001t0002g0108others(21): Show | 24 | HG00423.hp1 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.6345+466_6345+467d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | INFO_REALIGN_3_PRIME | chr4 | 86786399 | |||||
| chr4:86786505
|
A | G | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.6345+569A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86786505 | ||||||
| chr4:86786516
|
A | C | 1 | a0003c0002t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6345+580A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86786516 | ||||||
| chr4:86786523
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+587G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86786523 | ||||||
| chr4:86786825
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+889G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86786825 | ||||||
| chr4:86786932
|
T | C | 1 | a0006c0010t0003g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6345+996T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86786932 | ||||||
| chr4:86787042
|
T | C | 1 | a0002c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6345+1106T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86787042 | ||||||
| chr4:86787052
|
G | A | 6 | a0001c0003t0001g0035a0001c0003t0001g0037a0001c0003t0001g0038others(3): Show | 6 | NA18951.hp1 NA18953.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.6345+1116G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86787052 | ||||||
| chr4:86787103
|
C | CA | 5 | a0002c0001t0002g0158a0002c0001t0002g0159a0002c0001t0002g0160others(2): Show | 5 | HG00609.hp2 HG01891.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.6345+1179dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | INFO_REALIGN_3_PRIME | chr4 | 86787103 | |||||
| chr4:86787103
|
C | CAA | 5 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.6345+1178_6345+117 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | INFO_REALIGN_3_PRIME | chr4 | 86787103 | |||||
| chr4:86787120
|
T | C | 5 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(2): Show | 5 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.6345+1184T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86787120 | ||||||
| chr4:86787368
|
G | A | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.6345+1432G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86787368 | ||||||
| chr4:86787508
|
T | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+1572T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86787508 | ||||||
| chr4:86787575
|
A | G | 5 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.6345+1639A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86787575 | ||||||
| chr4:86787592
|
C | CA | 8 | a0003c0002t0001g0171a0003c0002t0001g0172a0003c0002t0001g0178others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.6345+1670dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | INFO_REALIGN_3_PRIME | chr4 | 86787592 | |||||
| chr4:86787592
|
C | CAA | 5 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.6345+1669_6345+167 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | INFO_REALIGN_3_PRIME | chr4 | 86787592 | |||||
| chr4:86787592
|
C | CAAAA | 9 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0003others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.6345+1667_6345+167 others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | INFO_REALIGN_3_PRIME | chr4 | 86787592 | |||||
| chr4:86788084
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+2148A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788084 | ||||||
| chr4:86788160
|
C | T | 2 | a0001c0003t0001g0090a0001c0003t0001g0093 | 2 | HG01074.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.6345+2224C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788160 | ||||||
| chr4:86788169
|
C | T | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.6345+2233C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788169 | ||||||
| chr4:86788170
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+2234G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788170 | ||||||
| chr4:86788257
|
C | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6345+2321C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788257 | ||||||
| chr4:86788263
|
G | A | 33 | a0003c0002t0002g0007a0003c0002t0002g0014a0003c0002t0002g0015others(30): Show | 33 | HG00639.hp1 HG00738.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.6345+2327G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788263 | ||||||
| chr4:86788464
|
G | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+2528G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788464 | ||||||
| chr4:86788519
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+2583C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788519 | ||||||
| chr4:86788620
|
G | T | 1 | a0002c0001t0002g0159 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6345+2684G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788620 | ||||||
| chr4:86788628
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+2692C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788628 | ||||||
| chr4:86788664
|
A | G | 1 | a0003c0002t0001g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.6345+2728A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788664 | ||||||
| chr4:86788715
|
A | G | 1 | a0003c0002t0005g0169 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.6345+2779A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788715 | ||||||
| chr4:86788920
|
A | G | 2 | a0003c0002t0002g0012a0008c0032t0003g0028 | 2 | HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6345+2984A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788920 | ||||||
| chr4:86788952
|
A | C | 1 | a0003c0002t0002g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6345+3016A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788952 | ||||||
| chr4:86788978
|
G | A | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.6345+3042G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86788978 | ||||||
| chr4:86789099
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+3163C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86789099 | ||||||
| chr4:86789218
|
T | A | 1 | a0008c0032t0003g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6345+3282T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86789218 | ||||||
| chr4:86789282
|
T | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+3346T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86789282 | ||||||
| chr4:86789385
|
T | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+3449T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86789385 | ||||||
| chr4:86789574
|
A | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+3638A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86789574 | ||||||
| chr4:86789664
|
T | TA | 6 | a0001c0004t0001g0070a0007c0007t0004g0132a0007c0007t0004g0167others(3): Show | 6 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.6345+3737dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | INFO_REALIGN_3_PRIME | chr4 | 86789664 | |||||
| chr4:86789842
|
C | CT | 13 | a0001c0003t0001g0062a0001c0003t0002g0006a0003c0002t0009g0188others(10): Show | 13 | HG00738.hp2 HG01099.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.6345+3922dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | INFO_REALIGN_3_PRIME | chr4 | 86789842 | |||||
| chr4:86789842
|
C | CTT | 6 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(3): Show | 6 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.6345+3921_6345+392 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | INFO_REALIGN_3_PRIME | chr4 | 86789842 | |||||
| chr4:86789888
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+3952A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86789888 | ||||||
| chr4:86790021
|
T | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+4085T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86790021 | ||||||
| chr4:86790029
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+4093A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86790029 | ||||||
| chr4:86790233
|
C | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+4297C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86790233 | ||||||
| chr4:86790333
|
G | A | 1 | a0003c0002t0009g0188 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.6345+4397G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86790333 | ||||||
| chr4:86790382
|
T | C | 1 | a0006c0010t0003g0196 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6345+4446T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86790382 | ||||||
| chr4:86790480
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+4544G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86790480 | ||||||
| chr4:86790540
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+4604C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86790540 | ||||||
| chr4:86790554
|
C | A | 1 | a0003c0002t0001g0178 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6345+4618C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86790554 | ||||||
| chr4:86790653
|
C | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+4717C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86790653 | ||||||
| chr4:86790677
|
G | A | 6 | a0001c0003t0001g0088a0001c0003t0001g0089a0001c0003t0001g0092others(3): Show | 6 | HG02135.hp1 NA18971.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.6345+4741G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86790677 | ||||||
| chr4:86790903
|
A | G | 36 | a0003c0002t0001g0171a0003c0002t0001g0172a0003c0002t0001g0178others(33): Show | 36 | HG00639.hp1 HG00738.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.6345+4967A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86790903 | ||||||
| chr4:86791039
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+5103C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86791039 | ||||||
| chr4:86791052
|
G | A | 4 | a0007c0007t0004g0167a0007c0007t0005g0175a0007c0007t0005g0179others(1): Show | 4 | HG02280.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.6345+5116G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86791052 | ||||||
| chr4:86791065
|
T | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+5129T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86791065 | ||||||
| chr4:86791071
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+5135G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86791071 | ||||||
| chr4:86791079
|
C | A | 24 | a0003c0002t0001g0091a0003c0002t0001g0168a0003c0002t0001g0170others(21): Show | 24 | HG00438.hp2 HG01071.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.6345+5143C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86791079 | ||||||
| chr4:86791155
|
C | T | 11 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.6345+5219C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86791155 | ||||||
| chr4:86791225
|
G | A | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.6345+5289G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86791225 | ||||||
| chr4:86791248
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6345+5312A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86791248 | ||||||
| chr4:86791390
|
A | T | 2 | a0002c0001t0002g0129a0002c0001t0002g0130 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.6345+5454A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86791390 | ||||||
| chr4:86791590
|
T | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-5284T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86791590 | ||||||
| chr4:86791598
|
G | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-5276G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86791598 | ||||||
| chr4:86791818
|
A | G | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.6346-5056A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86791818 | ||||||
| chr4:86791875
|
T | G | 60 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.6346-4999T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86791875 | ||||||
| chr4:86792000
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-4874G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792000 | ||||||
| chr4:86792040
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-4834C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792040 | ||||||
| chr4:86792061
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-4813G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792061 | ||||||
| chr4:86792062
|
G | T | 1 | a0005c0008t0002g0161 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6346-4812G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792062 | ||||||
| chr4:86792063
|
C | G | 1 | a0005c0008t0002g0161 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6346-4811C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792063 | ||||||
| chr4:86792064
|
A | C | 1 | a0005c0008t0002g0161 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6346-4810A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792064 | ||||||
| chr4:86792095
|
A | G | 1 | a0005c0008t0002g0161 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6346-4779A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792095 | ||||||
| chr4:86792104
|
C | T | 1 | a0003c0009t0001g0102 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.6346-4770C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792104 | ||||||
| chr4:86792196
|
G | A | 5 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.6346-4678G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792196 | ||||||
| chr4:86792226
|
C | T | 4 | a0002c0001t0002g0158a0002c0001t0002g0159a0002c0001t0002g0160others(1): Show | 4 | HG00609.hp2 HG02056.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.6346-4648C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792226 | ||||||
| chr4:86792433
|
T | C | 4 | a0004c0005t0004g0009a0004c0005t0005g0076a0004c0005t0005g0084others(1): Show | 4 | HG00738.hp2 HG01099.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.6346-4441T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792433 | ||||||
| chr4:86792495
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-4379G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792495 | ||||||
| chr4:86792592
|
TAA | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-4281_6346-428 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792592 | ||||||
| chr4:86792596
|
T | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-4278T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792596 | ||||||
| chr4:86792644
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-4230A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792644 | ||||||
| chr4:86792846
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-4028A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792846 | ||||||
| chr4:86792989
|
G | C | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.6346-3885G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86792989 | ||||||
| chr4:86793018
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-3856G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86793018 | ||||||
| chr4:86793118
|
CAT | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-3755_6346-375 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86793118 | ||||||
| chr4:86793191
|
A | G | 4 | a0001c0003t0001g0079a0001c0003t0001g0080a0001c0003t0001g0081others(1): Show | 4 | HG00140.hp2 HG01123.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.6346-3683A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86793191 | ||||||
| chr4:86793357
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-3517A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86793357 | ||||||
| chr4:86793376
|
G | A | 1 | a0003c0002t0005g0169 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.6346-3498G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86793376 | ||||||
| chr4:86793399
|
A | G | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.6346-3475A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86793399 | ||||||
| chr4:86793482
|
T | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-3392T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86793482 | ||||||
| chr4:86793660
|
G | T | 3 | a0003c0002t0001g0099a0003c0002t0001g0100a0003c0002t0001g0101 | 3 | HG02451.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.6346-3214G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86793660 | ||||||
| chr4:86793678
|
T | C | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.6346-3196T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86793678 | ||||||
| chr4:86793809
|
G | A | 4 | a0004c0005t0004g0001a0004c0005t0004g0003a0004c0005t0004g0004others(1): Show | 4 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.6346-3065G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86793809 | ||||||
| chr4:86793885
|
C | G | 33 | a0003c0002t0002g0007a0003c0002t0002g0014a0003c0002t0002g0015others(30): Show | 33 | HG00639.hp1 HG00738.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.6346-2989C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86793885 | ||||||
| chr4:86793909
|
T | TCTAAA | 92 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.6346-2963_6346-296 others(9): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | INFO_REALIGN_3_PRIME | chr4 | 86793909 | |||||
| chr4:86794079
|
T | A | 6 | a0003c0002t0002g0007a0003c0006t0003g0021a0003c0006t0003g0022others(3): Show | 6 | HG00639.hp1 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.6346-2795T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86794079 | ||||||
| chr4:86794264
|
C | CAG | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-2607_6346-260 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | INFO_REALIGN_3_PRIME | chr4 | 86794264 | |||||
| chr4:86794715
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-2159A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86794715 | ||||||
| chr4:86794816
|
A | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-2058A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86794816 | ||||||
| chr4:86794964
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-1910G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86794964 | ||||||
| chr4:86795045
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-1829A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86795045 | ||||||
| chr4:86795206
|
A | G | 12 | a0003c0002t0002g0007a0003c0006t0001g0030a0003c0006t0003g0021others(9): Show | 12 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.6346-1668A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86795206 | ||||||
| chr4:86795278
|
A | G | 1 | a0001c0004t0001g0069 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.6346-1596A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86795278 | ||||||
| chr4:86795294
|
A | G | 93 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0106others(90): Show | 93 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.6346-1580A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86795294 | ||||||
| chr4:86795334
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-1540A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86795334 | ||||||
| chr4:86795648
|
A | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-1226A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86795648 | ||||||
| chr4:86795806
|
A | G | 2 | a0001c0004t0001g0086a0001c0004t0007g0067 | 2 | NA19003.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.6346-1068A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86795806 | ||||||
| chr4:86795909
|
G | A | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.6346-965G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86795909 | ||||||
| chr4:86795936
|
G | A | 17 | a0003c0002t0002g0007a0003c0002t0002g0014a0003c0002t0002g0015others(14): Show | 17 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.6346-938G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86795936 | ||||||
| chr4:86795972
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-902G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86795972 | ||||||
| chr4:86795981
|
C | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-893C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86795981 | ||||||
| chr4:86795989
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-885A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86795989 | ||||||
| chr4:86795990
|
TAACA | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-880_6346-877d others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | INFO_REALIGN_3_PRIME | chr4 | 86795990 | |||||
| chr4:86795995
|
A | G | 1 | a0002c0001t0002g0149 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.6346-879A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86795995 | ||||||
| chr4:86796020
|
C | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-854C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86796020 | ||||||
| chr4:86796029
|
A | G | 1 | a0017c0022t0002g0114 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.6346-845A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86796029 | ||||||
| chr4:86796031
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-843A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86796031 | ||||||
| chr4:86796174
|
T | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-700T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86796174 | ||||||
| chr4:86796404
|
G | A | 17 | a0003c0002t0002g0007a0003c0002t0002g0014a0003c0002t0002g0015others(14): Show | 17 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.6346-470G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86796404 | ||||||
| chr4:86796483
|
A | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-391A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86796483 | ||||||
| chr4:86796484
|
A | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-390A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86796484 | ||||||
| chr4:86796547
|
C | T | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.6346-327C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86796547 | ||||||
| chr4:86796552
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6346-322G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86796552 | ||||||
| chr4:86796744
|
T | C | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.6346-130T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86796744 | ||||||
| chr4:86796858
|
T | C | 1 | a0004c0005t0004g0005 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.6346-16T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 40/47 | chr4 | 86796858 | ||||||
| chr4:86796963
|
T | TTCTATCT others(1): Show |
16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6401+37_6401+38ins others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr4 | 86796963 | |||||
| chr4:86797016
|
T | A | 9 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.6401+87T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797016 | ||||||
| chr4:86797050
|
G | A | 12 | a0003c0002t0002g0007a0003c0006t0001g0030a0003c0006t0003g0021others(9): Show | 12 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.6401+121G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797050 | ||||||
| chr4:86797126
|
G | A | 92 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.6401+197G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797126 | ||||||
| chr4:86797249
|
T | C | 1 | a0015c0021t0001g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6401+320T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797249 | ||||||
| chr4:86797320
|
T | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6401+391T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797320 | ||||||
| chr4:86797350
|
G | A | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.6401+421G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797350 | ||||||
| chr4:86797448
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6401+519C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797448 | ||||||
| chr4:86797456
|
T | C | 92 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.6401+527T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797456 | ||||||
| chr4:86797535
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6401+606A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797535 | ||||||
| chr4:86797582
|
C | G | 1 | a0001c0004t0001g0070 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.6401+653C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797582 | ||||||
| chr4:86797605
|
T | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6401+676T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797605 | ||||||
| chr4:86797637
|
A | T | 5 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.6401+708A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797637 | ||||||
| chr4:86797676
|
A | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6401+747A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797676 | ||||||
| chr4:86797729
|
C | CA | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6401+804dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr4 | 86797729 | |||||
| chr4:86797876
|
G | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6401+947G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797876 | ||||||
| chr4:86797919
|
G | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6401+990G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797919 | ||||||
| chr4:86797929
|
A | T | 2 | a0001c0004t0001g0086a0001c0004t0007g0067 | 2 | NA19003.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.6401+1000A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86797929 | ||||||
| chr4:86798256
|
G | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6402-845G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86798256 | ||||||
| chr4:86798309
|
T | A | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6402-792T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86798309 | ||||||
| chr4:86798530
|
A | G | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.6402-571A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86798530 | ||||||
| chr4:86798543
|
C | A | 10 | a0003c0002t0002g0007a0003c0006t0001g0030a0003c0006t0003g0021others(7): Show | 10 | HG00639.hp1 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.6402-558C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86798543 | ||||||
| chr4:86798578
|
G | GA | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6402-522dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr4 | 86798578 | |||||
| chr4:86798758
|
A | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6402-343A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86798758 | ||||||
| chr4:86798793
|
A | C | 2 | a0008c0014t0003g0025a0008c0014t0003g0026 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.6402-308A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86798793 | ||||||
| chr4:86798796
|
A | G | 2 | a0008c0014t0003g0025a0008c0014t0003g0026 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.6402-305A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86798796 | ||||||
| chr4:86798884
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6402-217A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86798884 | ||||||
| chr4:86798885
|
A | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6402-216A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86798885 | ||||||
| chr4:86798930
|
C | G | 1 | a0002c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6402-171C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 41/47 | chr4 | 86798930 | ||||||
| chr4:86799317
|
C | CT | 7 | a0001c0003t0001g0057a0001c0004t0001g0069a0003c0002t0002g0007others(4): Show | 7 | HG00639.hp1 HG01361.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.6505+129dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86799317 | |||||
| chr4:86799317
|
C | CTT | 7 | a0003c0006t0003g0021a0003c0006t0003g0022a0003c0006t0003g0023others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.6505+128_6505+129d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86799317 | |||||
| chr4:86799317
|
CT | C | 96 | a0001c0003t0001g0039a0001c0018t0001g0078a0002c0001t0002g0104others(93): Show | 96 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.6505+129delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86799317 | |||||
| chr4:86799369
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6505+165C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86799369 | ||||||
| chr4:86799378
|
CTCACTAC others(18): Show |
C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6505+195_6505+219d others(27): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86799378 | |||||
| chr4:86799614
|
A | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6505+410A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86799614 | ||||||
| chr4:86799619
|
C | T | 1 | a0001c0017t0001g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6505+415C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86799619 | ||||||
| chr4:86799825
|
C | CT | 59 | a0001c0003t0001g0064a0001c0003t0001g0068a0001c0004t0001g0050others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.6505+649dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86799825 | |||||
| chr4:86799825
|
C | CTT | 13 | a0001c0004t0008g0049a0002c0001t0002g0108a0002c0001t0002g0111others(10): Show | 13 | HG00423.hp1 HG00738.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.6505+648_6505+649d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86799825 | |||||
| chr4:86799825
|
CT | C | 5 | a0001c0003t0001g0060a0003c0002t0002g0014a0003c0002t0002g0016others(2): Show | 5 | HG02735.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.6505+649delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86799825 | |||||
| chr4:86799825
|
CTTTT | C | 14 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(11): Show | 14 | HG00738.hp2 HG01099.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.6505+646_6505+649d others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86799825 | |||||
| chr4:86799867
|
T | G | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6505+663T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86799867 | ||||||
| chr4:86799875
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6505+671G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86799875 | ||||||
| chr4:86800024
|
G | A | 1 | a0004c0005t0004g0001 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.6505+820G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86800024 | ||||||
| chr4:86800030
|
G | T | 1 | a0006c0010t0003g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6505+826G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86800030 | ||||||
| chr4:86800130
|
G | A | 1 | a0011c0015t0001g0041 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.6505+926G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86800130 | ||||||
| chr4:86800341
|
A | AT | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.6505+1151dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86800341 | |||||
| chr4:86800341
|
AT | A | 13 | a0001c0004t0001g0075a0001c0004t0002g0046a0002c0001t0002g0129others(10): Show | 13 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.6505+1151delT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86800341 | |||||
| chr4:86800570
|
T | C | 1 | a0003c0002t0005g0169 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.6505+1366T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86800570 | ||||||
| chr4:86800608
|
C | T | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6505+1404C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86800608 | ||||||
| chr4:86800634
|
A | G | 1 | a0002c0001t0002g0133 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.6505+1430A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86800634 | ||||||
| chr4:86800657
|
A | AAGAAAGA others(1): Show |
16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6505+1457_6505+146 others(12): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86800657 | |||||
| chr4:86801394
|
T | C | 16 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.6505+2190T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86801394 | ||||||
| chr4:86801817
|
A | G | 15 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.6506-1892A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86801817 | ||||||
| chr4:86801837
|
A | G | 5 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.6506-1872A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86801837 | ||||||
| chr4:86802145
|
T | TTG | 43 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(40): Show | 43 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.6506-1564_6506-156 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86802145 | ||||||
| chr4:86802145
|
T | TTGTG | 3 | a0002c0001t0002g0117a0002c0001t0002g0163a0002c0001t0002g0164 | 3 | HG01978.hp2 HG02056.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.6506-1564_6506-156 others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86802145 | ||||||
| chr4:86802145
|
TAG | T | 11 | a0002c0001t0002g0133a0002c0001t0002g0134a0002c0001t0002g0135others(8): Show | 11 | HG00140.hp1 HG01361.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.6506-1563_6506-156 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86802145 | ||||||
| chr4:86802146
|
A | AGT | 15 | a0001c0003t0001g0034a0001c0003t0001g0064a0001c0003t0001g0085others(12): Show | 15 | HG00639.hp1 HG01081.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.6506-1531_6506-153 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86802146 | |||||
| chr4:86802146
|
A | AGTGT | 8 | a0001c0003t0001g0044a0003c0002t0005g0169a0003c0006t0003g0023others(5): Show | 8 | HG01081.hp2 HG01175.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.6506-1533_6506-153 others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86802146 | |||||
| chr4:86802146
|
A | AGTGTGT | 2 | a0008c0014t0003g0025a0008c0014t0003g0026 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.6506-1535_6506-153 others(10): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86802146 | |||||
| chr4:86802146
|
A | T | 47 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(44): Show | 47 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.6506-1563A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86802146 | ||||||
| chr4:86802146
|
AGT | A | 8 | a0001c0003t0001g0060a0001c0003t0001g0068a0003c0002t0001g0173others(5): Show | 8 | HG02056.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.6506-1531_6506-153 others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86802146 | |||||
| chr4:86802146
|
AGTGT | A | 3 | a0001c0003t0001g0039a0001c0004t0001g0176a0003c0002t0003g0193 | 3 | NA18906.hp2 NA18953.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6506-1533_6506-153 others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86802146 | |||||
| chr4:86802168
|
T | C | 1 | a0001c0003t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.6506-1541T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86802168 | ||||||
| chr4:86802459
|
C | A | 92 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.6506-1250C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86802459 | ||||||
| chr4:86802626
|
G | T | 5 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(2): Show | 5 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.6506-1083G>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86802626 | ||||||
| chr4:86802935
|
G | C | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.6506-774G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86802935 | ||||||
| chr4:86803064
|
C | CTG | 59 | a0001c0003t0001g0034a0001c0003t0001g0083a0001c0004t0001g0050others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.6506-607_6506-606d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86803064 | |||||
| chr4:86803064
|
C | CTGTG | 23 | a0001c0003t0001g0088a0001c0003t0001g0089a0001c0003t0001g0092others(20): Show | 23 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.6506-609_6506-606d others(6): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86803064 | |||||
| chr4:86803064
|
C | CTGTGTG | 13 | a0001c0003t0001g0068a0001c0003t0001g0090a0001c0003t0001g0093others(10): Show | 13 | HG01074.hp2 HG01081.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.6506-611_6506-606d others(8): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86803064 | |||||
| chr4:86803064
|
C | CTGTGTGT others(1): Show |
8 | a0003c0002t0005g0169a0003c0009t0002g0144a0004c0005t0004g0009others(5): Show | 8 | HG00738.hp2 HG01099.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.6506-613_6506-606d others(10): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86803064 | |||||
| chr4:86803064
|
CTG | C | 17 | a0001c0003t0001g0035a0001c0003t0001g0037a0001c0003t0001g0038others(14): Show | 17 | HG01106.hp2 HG02486.hp2 HG03041.hp1 others(14): Show |
intron_variant | MODIFIER | c.6506-607_6506-606d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr4 | 86803064 | |||||
| chr4:86803104
|
A | G | 2 | a0010c0013t0003g0011a0010c0013t0003g0018 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.6506-605A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86803104 | ||||||
| chr4:86803154
|
G | A | 15 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.6506-555G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86803154 | ||||||
| chr4:86803190
|
T | C | 5 | a0003c0002t0002g0014a0003c0002t0002g0015a0003c0002t0002g0016others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.6506-519T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86803190 | ||||||
| chr4:86803467
|
A | G | 10 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.6506-242A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86803467 | ||||||
| chr4:86803685
|
T | G | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6506-24T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 42/47 | chr4 | 86803685 | ||||||
| chr4:86803948
|
T | A | 33 | a0003c0002t0002g0007a0003c0002t0002g0014a0003c0002t0002g0015others(30): Show | 33 | HG00639.hp1 HG00738.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.6654+91T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 43/47 | chr4 | 86803948 | ||||||
| chr4:86804123
|
A | G | 2 | a0008c0014t0003g0025a0008c0014t0003g0026 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.6654+266A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 43/47 | chr4 | 86804123 | ||||||
| chr4:86804123
|
A | T | 15 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.6654+266A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 43/47 | chr4 | 86804123 | ||||||
| chr4:86804444
|
G | C | 2 | a0002c0001t0002g0138a0002c0001t0002g0139 | 2 | NA18985.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.6654+587G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 43/47 | chr4 | 86804444 | ||||||
| chr4:86804759
|
C | T | 1 | a0001c0027t0001g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6655-520C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 43/47 | chr4 | 86804759 | ||||||
| chr4:86804830
|
G | A | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.6655-449G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 43/47 | chr4 | 86804830 | ||||||
| chr4:86805193
|
T | C | 1 | a0003c0002t0001g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.6655-86T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 43/47 | chr4 | 86805193 | ||||||
| chr4:86805637
|
G | A | 1 | a0003c0002t0001g0183 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.6745+268G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 44/47 | chr4 | 86805637 | ||||||
| chr4:86805832
|
T | G | 1 | a0002c0001t0002g0134 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.6745+463T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 44/47 | chr4 | 86805832 | ||||||
| chr4:86805922
|
G | A | 10 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.6745+553G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 44/47 | chr4 | 86805922 | ||||||
| chr4:86806296
|
A | G | 17 | a0003c0002t0002g0007a0003c0002t0002g0014a0003c0002t0002g0015others(14): Show | 17 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.6745+927A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 44/47 | chr4 | 86806296 | ||||||
| chr4:86806403
|
A | G | 15 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.6745+1034A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 44/47 | chr4 | 86806403 | ||||||
| chr4:86807175
|
A | T | 1 | a0001c0004t0001g0069 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.6746-385A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 44/47 | chr4 | 86807175 | ||||||
| chr4:86807190
|
A | G | 1 | a0001c0003t0001g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.6746-370A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 44/47 | chr4 | 86807190 | ||||||
| chr4:86807459
|
A | G | 2 | a0002c0001t0002g0138a0002c0001t0002g0139 | 2 | NA18985.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.6746-101A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 44/47 | chr4 | 86807459 | ||||||
| chr4:86807482
|
T | G | 1 | a0001c0017t0001g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6746-78T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 44/47 | chr4 | 86807482 | ||||||
| chr4:86807523
|
A | C | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.6746-37A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 44/47 | chr4 | 86807523 | ||||||
| chr4:86807931
|
G | C | 1 | a0001c0003t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.7083+34G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86807931 | ||||||
| chr4:86807968
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7083+71G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86807968 | ||||||
| chr4:86808101
|
T | A | 3 | a0002c0001t0002g0104a0002c0001t0002g0156a0002c0001t0002g0157 | 3 | HG04115.hp2 NA18968.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.7083+204T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86808101 | ||||||
| chr4:86808265
|
T | G | 15 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.7083+368T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86808265 | ||||||
| chr4:86808331
|
A | T | 2 | a0001c0003t0001g0062a0001c0003t0002g0006 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.7083+434A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86808331 | ||||||
| chr4:86808585
|
T | C | 5 | a0007c0007t0004g0132a0007c0007t0004g0167a0007c0007t0005g0175others(2): Show | 5 | HG02280.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.7083+688T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86808585 | ||||||
| chr4:86808653
|
A | G | 1 | a0002c0001t0002g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.7083+756A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86808653 | ||||||
| chr4:86808747
|
C | A | 1 | a0003c0002t0001g0186 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.7083+850C>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86808747 | ||||||
| chr4:86809257
|
T | G | 2 | a0001c0004t0001g0071a0001c0004t0001g0073 | 2 | HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.7084-512T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86809257 | ||||||
| chr4:86809479
|
G | A | 57 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(54): Show | 57 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.7084-290G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86809479 | ||||||
| chr4:86809500
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7084-269G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86809500 | ||||||
| chr4:86809590
|
A | C | 15 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.7084-179A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86809590 | ||||||
| chr4:86809622
|
C | T | 3 | a0003c0002t0001g0099a0003c0002t0001g0100a0003c0002t0001g0101 | 3 | HG02451.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.7084-147C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86809622 | ||||||
| chr4:86809678
|
G | A | 4 | a0004c0005t0004g0001a0004c0005t0004g0003a0004c0005t0004g0004others(1): Show | 4 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.7084-91G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 45/47 | chr4 | 86809678 | ||||||
| chr4:86810085
|
G | A | 92 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.7299+101G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 46/47 | chr4 | 86810085 | ||||||
| chr4:86810111
|
C | G | 15 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.7299+127C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 46/47 | chr4 | 86810111 | ||||||
| chr4:86810275
|
A | G | 1 | a0003c0002t0001g0183 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.7299+291A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 46/47 | chr4 | 86810275 | ||||||
| chr4:86810349
|
A | AT | 92 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.7299+372dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 46/47 | INFO_REALIGN_3_PRIME | chr4 | 86810349 | |||||
| chr4:86810401
|
T | C | 5 | a0004c0005t0004g0001a0004c0005t0004g0002a0004c0005t0004g0003others(2): Show | 5 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.7299+417T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 46/47 | chr4 | 86810401 | ||||||
| chr4:86810459
|
A | AATT | 92 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.7299+477_7299+479d others(5): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 46/47 | INFO_REALIGN_3_PRIME | chr4 | 86810459 | |||||
| chr4:86810795
|
G | C | 2 | a0002c0001t0002g0158a0002c0001t0002g0164 | 2 | HG00609.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.7300-251G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 46/47 | chr4 | 86810795 | ||||||
| chr4:86810845
|
T | A | 2 | a0003c0006t0001g0030a0003c0006t0010g0029 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.7300-201T>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 46/47 | chr4 | 86810845 | ||||||
| chr4:86810890
|
C | T | 1 | a0001c0004t0001g0053 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.7300-156C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 46/47 | chr4 | 86810890 | ||||||
| chr4:86811176
|
T | G | 15 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.7362+68T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86811176 | ||||||
| chr4:86811303
|
A | G | 1 | a0002c0001t0002g0115 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.7362+195A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86811303 | ||||||
| chr4:86811330
|
C | T | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.7362+222C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86811330 | ||||||
| chr4:86811332
|
A | G | 1 | a0021c0030t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.7362+224A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86811332 | ||||||
| chr4:86811478
|
A | G | 2 | a0002c0001t0002g0148a0002c0001t0002g0153 | 2 | HG02129.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.7362+370A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86811478 | ||||||
| chr4:86811483
|
C | G | 1 | a0001c0003t0001g0060 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.7362+375C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86811483 | ||||||
| chr4:86811602
|
G | A | 1 | a0012c0016t0006g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7362+494G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86811602 | ||||||
| chr4:86811649
|
A | G | 1 | a0001c0003t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.7362+541A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86811649 | ||||||
| chr4:86811711
|
C | G | 2 | a0008c0014t0003g0025a0008c0014t0003g0026 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.7362+603C>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86811711 | ||||||
| chr4:86811754
|
C | T | 10 | a0003c0002t0002g0007a0003c0006t0001g0030a0003c0006t0003g0021others(7): Show | 10 | HG00639.hp1 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.7362+646C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86811754 | ||||||
| chr4:86811932
|
G | C | 1 | a0003c0002t0001g0183 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.7362+824G>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86811932 | ||||||
| chr4:86812000
|
G | A | 59 | a0002c0001t0002g0104a0002c0001t0002g0105a0002c0001t0002g0107others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.7362+892G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86812000 | ||||||
| chr4:86812103
|
G | A | 14 | a0002c0001t0002g0106a0003c0002t0001g0091a0003c0002t0001g0183others(11): Show | 14 | HG00438.hp2 HG01071.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.7362+995G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86812103 | ||||||
| chr4:86812117
|
C | T | 1 | a0006c0010t0003g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7362+1009C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86812117 | ||||||
| chr4:86812124
|
A | C | 1 | a0006c0010t0003g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7362+1016A>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86812124 | ||||||
| chr4:86812125
|
A | G | 1 | a0006c0010t0003g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7362+1017A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86812125 | ||||||
| chr4:86812139
|
T | C | 1 | a0006c0010t0003g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7362+1031T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86812139 | ||||||
| chr4:86812173
|
A | G | 1 | a0006c0010t0003g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7362+1065A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86812173 | ||||||
| chr4:86812182
|
C | T | 10 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.7362+1074C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86812182 | ||||||
| chr4:86812309
|
C | CA | 66 | a0001c0003t0001g0037a0001c0003t0001g0065a0001c0003t0001g0081others(63): Show | 66 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.7362+1225dupA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | INFO_REALIGN_3_PRIME | chr4 | 86812309 | |||||
| chr4:86812309
|
CA | C | 25 | a0001c0004t0001g0052a0002c0001t0002g0104a0002c0001t0002g0106others(22): Show | 25 | HG00639.hp1 HG01099.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.7362+1225delA | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | INFO_REALIGN_3_PRIME | chr4 | 86812309 | |||||
| chr4:86812309
|
CAAAAAAA others(2): Show |
C | 15 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0004g0002others(12): Show | 15 | HG00738.hp2 HG01099.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.7362+1217_7362+122 others(13): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | INFO_REALIGN_3_PRIME | chr4 | 86812309 | |||||
| chr4:86812394
|
A | G | 1 | a0004c0005t0004g0002 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.7362+1286A>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86812394 | ||||||
| chr4:86812619
|
T | G | 4 | a0002c0001t0002g0158a0002c0001t0002g0159a0002c0001t0002g0160others(1): Show | 4 | HG00609.hp2 HG02056.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.7362+1511T>G | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86812619 | ||||||
| chr4:86813649
|
ACTC | A | 2 | a0001c0004t0001g0071a0001c0004t0001g0073 | 2 | HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.7363-804_7363-802d others(5): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | INFO_REALIGN_3_PRIME | chr4 | 86813649 | |||||
| chr4:86813679
|
G | A | 8 | a0002c0001t0002g0133a0002c0001t0002g0134a0002c0001t0002g0135others(5): Show | 8 | HG02135.hp2 NA18612.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.7363-777G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86813679 | ||||||
| chr4:86814000
|
C | CT | 31 | a0001c0003t0001g0065a0001c0003t0001g0081a0001c0003t0001g0082others(28): Show | 31 | HG00438.hp1 HG01081.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.7363-430dupT | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | INFO_REALIGN_3_PRIME | chr4 | 86814000 | |||||
| chr4:86814000
|
CTT | C | 10 | a0003c0002t0005g0169a0004c0005t0004g0001a0004c0005t0005g0076others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.7363-431_7363-430d others(4): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | INFO_REALIGN_3_PRIME | chr4 | 86814000 | |||||
| chr4:86814000
|
CTTT | C | 5 | a0004c0005t0004g0002a0004c0005t0004g0003a0004c0005t0004g0004others(2): Show | 5 | HG01123.hp2 HG01192.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.7363-432_7363-430d others(5): Show |
PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | INFO_REALIGN_3_PRIME | chr4 | 86814000 | |||||
| chr4:86814161
|
G | A | 1 | a0002c0001t0002g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.7363-295G>A | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86814161 | ||||||
| chr4:86814208
|
T | C | 17 | a0003c0002t0002g0007a0003c0002t0002g0014a0003c0002t0002g0015others(14): Show | 17 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.7363-248T>C | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86814208 | ||||||
| chr4:86814296
|
C | T | 1 | a0016c0019t0002g0045 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.7363-160C>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86814296 | ||||||
| chr4:86814327
|
A | T | 1 | a0002c0011t0001g0113 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.7363-129A>T | PTPN13 | ENSG00000163629.13 | transcript | ENST00000411767.7 | protein_coding | 47/47 | chr4 | 86814327 |