Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2185 |
|---|---|
| ensemblid | ENSG00000120899.18 |
| hgncid | 9612 |
| symbol | PTK2B |
| name | protein tyrosine kinase 2 beta |
| refseq_nuc | NM_173176.3 |
| refseq_prot | NP_775268.1 |
| ensembl_nuc | ENST00000346049.10 |
| ensembl_prot | ENSP00000332816.6 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 27325552 |
| end | 27459386 |
| strand | + |
| ver | v1.2 |
| region | chr8:27325552-27459386 |
| region5000 | chr8:27320552-27464386 |
| regionname0 | PTK2B_chr8_27325552_27459386 |
| regionname5000 | PTK2B_chr8_27320552_27464386 |
| 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 | 1009 | 184 | 65 | 34 | 70 | 5 | 9 | 53 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002 | 0/1 | 1009 | 133 | 25 | 36 | 53 | 5 | 13 | 39 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0003 | 0/0 | 1009 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0004 | 0/0 | 1009 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0005 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0006 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0007 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0008 | 0/0 | 616 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0009 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0010 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0011 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| 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 | 3030 | 68 | 28 | 14 | 18 | 3 | 5 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0002 | 1/0 | 3030 | 62 | 7 | 8 | 41 | 2 | 3 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0003 | 0/1 | 3030 | 58 | 8 | 18 | 24 | 3 | 4 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0004 | 0/0 | 3030 | 31 | 0 | 6 | 18 | 1 | 6 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0005 | 0/0 | 3030 | 19 | 0 | 8 | 8 | 0 | 3 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0006 | 0/0 | 3030 | 19 | 13 | 3 | 2 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0007 | 0/0 | 3030 | 11 | 5 | 6 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0008 | 0/0 | 3030 | 9 | 9 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0009 | 0/0 | 3030 | 8 | 1 | 1 | 6 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0010 | 0/0 | 3030 | 8 | 8 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0011 | 0/0 | 3030 | 6 | 0 | 1 | 5 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0012 | 0/0 | 3030 | 4 | 0 | 3 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0013 | 0/0 | 3030 | 3 | 2 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0014 | 0/0 | 3030 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0015 | 0/0 | 3030 | 2 | 0 | 0 | 2 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0016 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0017 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0018 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0019 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0020 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0021 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0022 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0023 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0024 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0025 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0026 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0027 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0028 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0029 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0030 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0031 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0032 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| c0033 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| 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 | 1/0 | 1045 | 115 | 23 | 21 | 61 | 3 | 6 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| t0002 | 0/1 | 1045 | 103 | 14 | 24 | 50 | 4 | 10 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| t0003 | 0/0 | 1045 | 102 | 54 | 22 | 18 | 3 | 5 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| t0004 | 0/0 | 1045 | 6 | 1 | 4 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| t0005 | 0/0 | 1045 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| t0006 | 0/0 | 1045 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0134 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3030 | 68 | 28 | 14 | 18 | 3 | 5 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0002 | 1/0 | 3030 | 62 | 7 | 8 | 41 | 2 | 3 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0007 | 0/0 | 3030 | 11 | 5 | 6 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0008 | 0/0 | 3030 | 9 | 9 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0009 | 0/0 | 3030 | 8 | 1 | 1 | 6 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0010 | 0/0 | 3030 | 8 | 8 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0011 | 0/0 | 3030 | 6 | 0 | 1 | 5 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0012 | 0/0 | 3030 | 4 | 0 | 3 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0013 | 0/0 | 3030 | 3 | 2 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0021 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0022 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0025 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0027 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0030 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0003 | 0/1 | 3030 | 58 | 8 | 18 | 24 | 3 | 4 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0004 | 0/0 | 3030 | 31 | 0 | 6 | 18 | 1 | 6 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0005 | 0/0 | 3030 | 19 | 0 | 8 | 8 | 0 | 3 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0006 | 0/0 | 3030 | 19 | 13 | 3 | 2 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0017 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0018 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0023 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0024 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0026 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0031 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0003c0014 | 0/0 | 3030 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0004c0015 | 0/0 | 3030 | 2 | 0 | 0 | 2 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0005c0016 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0006c0028 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0007c0029 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0008c0020 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0009c0019 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0010c0032 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0011c0033 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0003 | 0/0 | 4074 | 67 | 28 | 13 | 18 | 3 | 5 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0001t0005 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0002t0001 | 1/0 | 4074 | 62 | 7 | 8 | 41 | 2 | 3 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0007t0003 | 0/0 | 4074 | 11 | 5 | 6 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0008t0003 | 0/0 | 4074 | 9 | 9 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0009t0002 | 0/0 | 4074 | 8 | 1 | 1 | 6 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0010t0003 | 0/0 | 4074 | 8 | 8 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0011t0001 | 0/0 | 4074 | 6 | 0 | 1 | 5 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0012t0004 | 0/0 | 4074 | 4 | 0 | 3 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0013t0003 | 0/0 | 4074 | 3 | 2 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0021t0004 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0022t0002 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0025t0001 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0027t0003 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0001c0030t0002 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0003t0002 | 0/1 | 4074 | 56 | 8 | 17 | 23 | 3 | 4 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0003t0004 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0003t0006 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0004t0002 | 0/0 | 4074 | 31 | 0 | 6 | 18 | 1 | 6 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0005t0001 | 0/0 | 4074 | 19 | 0 | 8 | 8 | 0 | 3 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0006t0001 | 0/0 | 4074 | 18 | 12 | 3 | 2 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0006t0002 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0017t0002 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0018t0002 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0023t0001 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0024t0001 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0026t0001 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0002c0031t0001 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0003c0014t0003 | 0/0 | 4074 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0004c0015t0001 | 0/0 | 4074 | 2 | 0 | 0 | 2 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0005c0016t0002 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0006c0028t0001 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0007c0029t0001 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0008c0020t0002 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0009c0019t0002 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0010c0032t0003 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| a0011c0033t0001 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | copy fasta | chr8 | 27320552 | 27464386 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0134 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0007t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0007t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0007t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0007t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0007t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0007t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0007t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0007t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0007t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0007t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0007t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0008t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0008t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0008t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0008t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0008t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0008t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0008t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0008t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0008t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0009t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0009t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0009t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0009t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0009t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0009t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0009t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0009t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0010t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0010t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0010t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0010t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0010t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0010t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0010t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0010t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0011t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0011t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0011t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0011t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0011t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0011t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0012t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0012t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0012t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0012t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0013t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0013t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0013t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0021t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0022t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0025t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0027t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0001c0030t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0003t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0004t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0005t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0006t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0017t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0018t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0023t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0024t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0026t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0002c0031t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0003c0014t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0003c0014t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0004c0015t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0004c0015t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0005c0016t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0006c0028t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0007c0029t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0008c0020t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0009c0019t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0010c0032t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| a0011c0033t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0132 | EUR | GBR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00099 | hp2 | a0002 | c0003 | t0002 | g0265 | EUR | GBR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0124 | EUR | FIN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0096 | EUR | FIN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00408 | hp1 | a0002 | c0005 | t0001 | g0202 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00408 | hp2 | a0002 | c0003 | t0002 | g0239 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00423 | hp1 | a0001 | c0009 | t0002 | g0237 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00423 | hp2 | a0001 | c0009 | t0002 | g0106 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00438 | hp2 | a0002 | c0004 | t0002 | g0100 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00609 | hp1 | a0002 | c0005 | t0001 | g0074 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00609 | hp2 | a0001 | c0009 | t0002 | g0125 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00621 | hp2 | a0005 | c0016 | t0002 | g0105 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00639 | hp1 | a0001 | c0013 | t0003 | g0302 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00639 | hp2 | a0002 | c0005 | t0001 | g0002 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00673 | hp2 | a0002 | c0003 | t0002 | g0222 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00733 | hp2 | a0002 | c0003 | t0004 | g0272 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00735 | hp1 | a0002 | c0003 | t0002 | g0023 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00735 | hp2 | a0001 | c0007 | t0003 | g0135 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00738 | hp1 | a0002 | c0006 | t0001 | g0010 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00741 | hp1 | a0002 | c0003 | t0002 | g0261 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG00741 | hp2 | a0002 | c0004 | t0002 | g0094 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0060 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01069 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01070 | hp1 | a0002 | c0006 | t0001 | g0038 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01070 | hp2 | a0001 | c0007 | t0003 | g0277 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01071 | hp1 | a0001 | c0007 | t0003 | g0278 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01071 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01074 | hp2 | a0002 | c0003 | t0002 | g0263 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01081 | hp1 | a0001 | c0012 | t0004 | g0057 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01081 | hp2 | a0002 | c0024 | t0001 | g0086 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01099 | hp1 | a0003 | c0014 | t0003 | g0061 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01099 | hp2 | a0002 | c0004 | t0002 | g0246 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01106 | hp1 | a0002 | c0003 | t0002 | g0055 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01106 | hp2 | a0002 | c0003 | t0002 | g0266 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01109 | hp1 | a0002 | c0005 | t0001 | g0002 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0273 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01168 | hp1 | a0002 | c0004 | t0002 | g0244 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01169 | hp1 | a0003 | c0014 | t0003 | g0043 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01169 | hp2 | a0002 | c0004 | t0002 | g0245 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01175 | hp1 | a0002 | c0003 | t0002 | g0253 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01175 | hp2 | a0001 | c0012 | t0004 | g0211 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01192 | hp1 | a0001 | c0011 | t0001 | g0078 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01255 | hp1 | a0002 | c0004 | t0002 | g0298 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01256 | hp2 | a0002 | c0005 | t0001 | g0194 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01257 | hp1 | a0002 | c0003 | t0002 | g0067 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01257 | hp2 | a0002 | c0003 | t0002 | g0264 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01258 | hp1 | a0002 | c0003 | t0002 | g0004 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01258 | hp2 | a0002 | c0005 | t0001 | g0195 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01261 | hp1 | a0002 | c0003 | t0002 | g0247 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01261 | hp2 | a0001 | c0009 | t0002 | g0018 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01346 | hp1 | a0002 | c0003 | t0002 | g0056 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01361 | hp1 | a0002 | c0006 | t0001 | g0070 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01361 | hp2 | a0002 | c0003 | t0002 | g0004 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0097 | EUR | IBS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01515 | hp2 | a0002 | c0004 | t0002 | g0248 | EUR | IBS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01516 | hp1 | a0002 | c0006 | t0001 | g0068 | EUR | IBS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01516 | hp2 | a0002 | c0003 | t0002 | g0260 | EUR | IBS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01884 | hp1 | a0002 | c0003 | t0002 | g0251 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01928 | hp1 | a0002 | c0005 | t0001 | g0033 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01943 | hp2 | a0002 | c0005 | t0001 | g0031 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01978 | hp1 | a0002 | c0004 | t0002 | g0242 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01978 | hp2 | a0001 | c0012 | t0004 | g0053 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01993 | hp1 | a0001 | c0007 | t0003 | g0136 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01993 | hp2 | a0002 | c0003 | t0002 | g0069 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02004 | hp2 | a0002 | c0003 | t0002 | g0299 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02015 | hp1 | a0002 | c0003 | t0002 | g0219 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02040 | hp2 | a0002 | c0004 | t0002 | g0107 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02056 | hp2 | a0001 | c0011 | t0001 | g0148 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02071 | hp1 | a0002 | c0004 | t0002 | g0209 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02074 | hp1 | a0002 | c0004 | t0002 | g0111 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02074 | hp2 | a0002 | c0003 | t0002 | g0283 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02080 | hp2 | a0002 | c0003 | t0002 | g0274 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02145 | hp2 | a0002 | c0023 | t0001 | g0123 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02165 | hp1 | a0002 | c0003 | t0002 | g0258 | EAS | CDX | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02165 | hp2 | a0002 | c0031 | t0001 | g0156 | EAS | CDX | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0318 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02258 | hp1 | a0001 | c0008 | t0003 | g0316 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02258 | hp2 | a0002 | c0003 | t0002 | g0256 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02273 | hp1 | a0002 | c0003 | t0002 | g0058 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02273 | hp2 | a0001 | c0007 | t0003 | g0189 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02280 | hp2 | a0002 | c0003 | t0002 | g0249 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02300 | hp1 | a0001 | c0007 | t0003 | g0137 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02300 | hp2 | a0002 | c0005 | t0001 | g0026 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02523 | hp1 | a0002 | c0003 | t0002 | g0300 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02615 | hp1 | a0001 | c0030 | t0002 | g0007 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02615 | hp2 | a0002 | c0006 | t0001 | g0286 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02622 | hp1 | a0002 | c0006 | t0001 | g0323 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02630 | hp1 | a0002 | c0006 | t0001 | g0291 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02630 | hp2 | a0001 | c0007 | t0003 | g0303 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02647 | hp1 | a0001 | c0010 | t0003 | g0232 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02647 | hp2 | a0006 | c0028 | t0001 | g0179 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02698 | hp2 | a0002 | c0004 | t0002 | g0112 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02717 | hp1 | a0001 | c0008 | t0003 | g0114 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0294 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02723 | hp1 | a0001 | c0013 | t0003 | g0304 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02723 | hp2 | a0001 | c0008 | t0003 | g0319 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02809 | hp1 | a0001 | c0010 | t0003 | g0285 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02809 | hp2 | a0002 | c0003 | t0002 | g0321 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02895 | hp1 | a0001 | c0007 | t0003 | g0280 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02895 | hp2 | a0001 | c0010 | t0003 | g0230 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02896 | hp1 | a0001 | c0008 | t0003 | g0292 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02896 | hp2 | a0002 | c0006 | t0001 | g0234 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02897 | hp1 | a0001 | c0007 | t0003 | g0281 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02897 | hp2 | a0002 | c0006 | t0001 | g0290 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02922 | hp1 | a0010 | c0032 | t0003 | g0284 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0226 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02965 | hp2 | a0002 | c0017 | t0002 | g0252 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02970 | hp1 | a0001 | c0008 | t0003 | g0320 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03041 | hp1 | a0001 | c0010 | t0003 | g0229 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0176 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03098 | hp1 | a0001 | c0027 | t0003 | g0293 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03098 | hp2 | a0001 | c0010 | t0003 | g0233 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03130 | hp1 | a0001 | c0013 | t0003 | g0301 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03130 | hp2 | a0002 | c0006 | t0001 | g0062 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0296 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03195 | hp1 | a0002 | c0006 | t0001 | g0020 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03195 | hp2 | a0002 | c0026 | t0001 | g0238 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03209 | hp1 | a0002 | c0006 | t0001 | g0287 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03209 | hp2 | a0001 | c0008 | t0003 | g0295 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03225 | hp2 | a0001 | c0010 | t0003 | g0289 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03239 | hp1 | a0001 | c0012 | t0004 | g0030 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03239 | hp2 | a0002 | c0003 | t0002 | g0259 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03486 | hp2 | a0002 | c0003 | t0002 | g0267 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03490 | hp1 | a0002 | c0004 | t0002 | g0109 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03490 | hp2 | a0002 | c0003 | t0002 | g0275 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03516 | hp1 | a0002 | c0003 | t0002 | g0180 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0276 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0174 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03669 | hp1 | a0002 | c0004 | t0002 | g0225 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03669 | hp2 | a0002 | c0005 | t0001 | g0204 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03704 | hp1 | a0002 | c0004 | t0002 | g0110 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03704 | hp2 | a0002 | c0003 | t0002 | g0262 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0166 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03927 | hp1 | a0002 | c0004 | t0002 | g0099 | SAS | BEB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03927 | hp2 | a0002 | c0005 | t0001 | g0203 | SAS | BEB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG04115 | hp1 | a0002 | c0004 | t0002 | g0224 | SAS | STU | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG04115 | hp2 | a0002 | c0005 | t0001 | g0309 | SAS | STU | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0196 | SAS | STU | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | STU | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | YRI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18522 | hp2 | a0001 | c0007 | t0003 | g0279 | AFR | YRI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18906 | hp1 | a0002 | c0003 | t0002 | g0236 | AFR | YRI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | YRI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18943 | hp1 | a0002 | c0006 | t0001 | g0126 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18943 | hp2 | a0001 | c0009 | t0002 | g0313 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18946 | hp1 | a0002 | c0004 | t0002 | g0250 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18946 | hp2 | a0001 | c0009 | t0002 | g0103 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18947 | hp2 | a0002 | c0003 | t0002 | g0241 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18949 | hp1 | a0001 | c0011 | t0001 | g0165 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18949 | hp2 | a0008 | c0020 | t0002 | g0014 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18960 | hp2 | a0002 | c0003 | t0002 | g0255 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18961 | hp1 | a0002 | c0003 | t0002 | g0223 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18961 | hp2 | a0001 | c0011 | t0001 | g0151 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18962 | hp1 | a0001 | c0011 | t0001 | g0142 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18962 | hp2 | a0002 | c0004 | t0002 | g0210 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18966 | hp1 | a0002 | c0003 | t0002 | g0271 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18966 | hp2 | a0004 | c0015 | t0001 | g0193 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18967 | hp2 | a0002 | c0003 | t0002 | g0307 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18968 | hp2 | a0002 | c0004 | t0002 | g0011 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18969 | hp2 | a0002 | c0003 | t0002 | g0311 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18970 | hp1 | a0002 | c0005 | t0001 | g0201 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18970 | hp2 | a0001 | c0011 | t0001 | g0098 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18979 | hp1 | a0002 | c0005 | t0001 | g0083 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18979 | hp2 | a0002 | c0003 | t0002 | g0216 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18980 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18981 | hp2 | a0002 | c0004 | t0002 | g0108 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18983 | hp1 | a0002 | c0003 | t0006 | g0044 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18986 | hp2 | a0002 | c0004 | t0002 | g0104 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18990 | hp1 | a0002 | c0003 | t0002 | g0012 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18990 | hp2 | a0002 | c0003 | t0002 | g0308 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18993 | hp1 | a0002 | c0003 | t0002 | g0217 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18994 | hp1 | a0001 | c0009 | t0002 | g0310 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18994 | hp2 | a0002 | c0003 | t0002 | g0220 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18995 | hp2 | a0007 | c0029 | t0001 | g0153 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18999 | hp1 | a0002 | c0003 | t0002 | g0240 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18999 | hp2 | a0004 | c0015 | t0001 | g0200 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19002 | hp2 | a0011 | c0033 | t0001 | g0154 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19003 | hp1 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19005 | hp1 | a0002 | c0003 | t0002 | g0270 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19007 | hp1 | a0002 | c0004 | t0002 | g0215 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19007 | hp2 | a0002 | c0005 | t0001 | g0084 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19009 | hp2 | a0002 | c0003 | t0002 | g0221 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19012 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0305 | AFR | LWK | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19030 | hp2 | a0002 | c0006 | t0001 | g0006 | AFR | LWK | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19043 | hp1 | a0002 | c0018 | t0002 | g0089 | AFR | LWK | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19043 | hp2 | a0001 | c0021 | t0004 | g0009 | AFR | LWK | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19056 | hp1 | a0002 | c0006 | t0001 | g0213 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19056 | hp2 | a0002 | c0005 | t0001 | g0198 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19057 | hp1 | a0002 | c0003 | t0002 | g0218 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19068 | hp1 | a0002 | c0004 | t0002 | g0141 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19070 | hp1 | a0002 | c0005 | t0001 | g0085 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19074 | hp1 | a0002 | c0004 | t0002 | g0191 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19077 | hp1 | a0002 | c0004 | t0002 | g0013 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19082 | hp1 | a0002 | c0005 | t0001 | g0199 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19087 | hp2 | a0009 | c0019 | t0002 | g0102 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19090 | hp2 | a0002 | c0004 | t0002 | g0208 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19091 | hp2 | a0002 | c0003 | t0002 | g0254 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19240 | hp1 | a0001 | c0008 | t0003 | g0315 | AFR | YRI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA19240 | hp2 | a0001 | c0009 | t0002 | g0087 | AFR | YRI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA20129 | hp1 | a0002 | c0006 | t0002 | g0317 | AFR | ASW | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA20129 | hp2 | a0001 | c0007 | t0003 | g0177 | AFR | ASW | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0024 | EUR | TSI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA20805 | hp2 | a0002 | c0003 | t0002 | g0207 | EUR | TSI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA20905 | hp1 | a0002 | c0003 | t0002 | g0268 | SAS | GIH | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0147 | SAS | GIH | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG01123 | hp2 | a0002 | c0005 | t0001 | g0197 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0322 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02109 | hp2 | a0001 | c0008 | t0003 | g0243 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02486 | hp1 | a0001 | c0010 | t0003 | g0231 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02486 | hp2 | a0001 | c0008 | t0003 | g0314 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG02559 | hp2 | a0002 | c0003 | t0002 | g0269 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG06807 | hp1 | a0001 | c0010 | t0003 | g0297 | AFR | USA | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| HG06807 | hp2 | a0002 | c0006 | t0001 | g0063 | AFR | USA | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA18955 | hp2 | a0002 | c0004 | t0002 | g0101 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA20300 | hp1 | a0001 | c0025 | t0001 | g0019 | AFR | USA | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA20300 | hp2 | a0001 | c0022 | t0002 | g0008 | AFR | USA | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA21309 | hp1 | a0002 | c0006 | t0001 | g0282 | AFR | LWK | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| NA21309 | hp2 | a0002 | c0006 | t0001 | g0092 | AFR | LWK | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0002 | g0257 | REF | REF | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0134 | REF | REF | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:27397637
|
G | A | 1 | a0005 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.53G>A | p.Arg18Gln | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/31 | 220/4074 | 53/3030 | 18/1009 | chr8 | 27397637 | ||
| chr8:27430984
|
A | G | 1 | a0011 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.778A>G | p.Ile260Val | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 8/31 | 945/4074 | 778/3030 | 260/1009 | chr8 | 27430984 | ||
| chr8:27430997
|
C | A | 1 | a0003 | 2 | HG01099.hp1 HG01169.hp1 |
missense_variant | MODERATE | c.791C>A | p.Thr264Asn | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 8/31 | 958/4074 | 791/3030 | 264/1009 | chr8 | 27430997 | ||
| chr8:27434530
|
G | A | 1 | a0006 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1163G>A | p.Arg388Gln | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/31 | 1330/4074 | 1163/3030 | 388/1009 | chr8 | 27434530 | ||
| chr8:27435791
|
G | A | 1 | a0004 | 2 | NA18966.hp2 NA18999.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1241G>A | p.Gly414Glu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 14/31 | 1408/4074 | 1241/3030 | 414/1009 | chr8 | 27435791 | ||
| chr8:27437873
|
G | A | 1 | a0007 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.1636G>A | p.Val546Met | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/31 | 1803/4074 | 1636/3030 | 546/1009 | chr8 | 27437873 | ||
| chr8:27440239
|
G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant&splice_region_variant | MODERATE | c.1837G>T | p.Val613Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2004/4074 | 1837/3030 | 613/1009 | chr8 | 27440239 | ||
| chr8:27440247
|
G | C | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1845G>C | p.Met615Ile | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2012/4074 | 1845/3030 | 615/1009 | chr8 | 27440247 | ||
| chr8:27440251
|
G | T | 1 | a0008 | 1 | NA18949.hp2 | stop_gained | HIGH | c.1849G>T | p.Glu617* | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2016/4074 | 1849/3030 | 617/1009 | chr8 | 27440251 | ||
| chr8:27440254
|
A | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1852A>T | p.Ile618Phe | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2019/4074 | 1852/3030 | 618/1009 | chr8 | 27440254 | ||
| chr8:27440263
|
T | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1861T>A | p.Phe621Ile | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2028/4074 | 1861/3030 | 621/1009 | chr8 | 27440263 | ||
| chr8:27440264
|
T | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1862T>A | p.Phe621Tyr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2029/4074 | 1862/3030 | 621/1009 | chr8 | 27440264 | ||
| chr8:27440265
|
T | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1863T>A | p.Phe621Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2030/4074 | 1863/3030 | 621/1009 | chr8 | 27440265 | ||
| chr8:27440266
|
G | C | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1864G>C | p.Gly622Arg | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2031/4074 | 1864/3030 | 622/1009 | chr8 | 27440266 | ||
| chr8:27440267
|
G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1865G>T | p.Gly622Val | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2032/4074 | 1865/3030 | 622/1009 | chr8 | 27440267 | ||
| chr8:27440272
|
C | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1870C>A | p.Gln624Lys | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2037/4074 | 1870/3030 | 624/1009 | chr8 | 27440272 | ||
| chr8:27440274
|
G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1872G>T | p.Gln624His | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2039/4074 | 1872/3030 | 624/1009 | chr8 | 27440274 | ||
| chr8:27440275
|
C | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1873C>T | p.Pro625Ser | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2040/4074 | 1873/3030 | 625/1009 | chr8 | 27440275 | ||
| chr8:27440279
|
T | G | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1877T>G | p.Phe626Cys | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2044/4074 | 1877/3030 | 626/1009 | chr8 | 27440279 | ||
| chr8:27440282
|
T | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1880T>A | p.Phe627Tyr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2047/4074 | 1880/3030 | 627/1009 | chr8 | 27440282 | ||
| chr8:27440285
|
G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1883G>T | p.Trp628Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2050/4074 | 1883/3030 | 628/1009 | chr8 | 27440285 | ||
| chr8:27440286
|
G | C | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1884G>C | p.Trp628Cys | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2051/4074 | 1884/3030 | 628/1009 | chr8 | 27440286 | ||
| chr8:27440288
|
T | C | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1886T>C | p.Leu629Pro | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2053/4074 | 1886/3030 | 629/1009 | chr8 | 27440288 | ||
| chr8:27440294
|
A | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1892A>T | p.Asn631Ile | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2059/4074 | 1892/3030 | 631/1009 | chr8 | 27440294 | ||
| chr8:27440295
|
C | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1893C>A | p.Asn631Lys | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2060/4074 | 1893/3030 | 631/1009 | chr8 | 27440295 | ||
| chr8:27440298
|
G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1896G>T | p.Lys632Asn | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2063/4074 | 1896/3030 | 632/1009 | chr8 | 27440298 | ||
| chr8:27440299
|
G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1897G>T | p.Asp633Tyr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2064/4074 | 1897/3030 | 633/1009 | chr8 | 27440299 | ||
| chr8:27440300
|
A | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1898A>T | p.Asp633Val | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2065/4074 | 1898/3030 | 633/1009 | chr8 | 27440300 | ||
| chr8:27440302
|
G | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1900G>A | p.Val634Ile | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2067/4074 | 1900/3030 | 634/1009 | chr8 | 27440302 | ||
| chr8:27440303
|
T | C | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1901T>C | p.Val634Ala | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2068/4074 | 1901/3030 | 634/1009 | chr8 | 27440303 | ||
| chr8:27440306
|
T | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1904T>A | p.Ile635Asn | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2071/4074 | 1904/3030 | 635/1009 | chr8 | 27440306 | ||
| chr8:27440311
|
G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1909G>T | p.Val637Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2076/4074 | 1909/3030 | 637/1009 | chr8 | 27440311 | ||
| chr8:27440319
|
G | C | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1917G>C | p.Glu639Asp | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2084/4074 | 1917/3030 | 639/1009 | chr8 | 27440319 | ||
| chr8:27440320
|
A | T | 1 | a0008 | 1 | NA18949.hp2 | stop_gained | HIGH | c.1918A>T | p.Lys640* | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2085/4074 | 1918/3030 | 640/1009 | chr8 | 27440320 | ||
| chr8:27445804
|
G | T | 1 | a0010 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.2225G>T | p.Gly742Val | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/31 | 2392/4074 | 2225/3030 | 742/1009 | chr8 | 27445804 | ||
| chr8:27445857
|
G | A | 1 | a0009 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.2278G>A | p.Val760Ile | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/31 | 2445/4074 | 2278/3030 | 760/1009 | chr8 | 27445857 | ||
| chr8:27451068
|
A | C | 5 | a0002a0004a0005others(2): Show | 138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
missense_variant | MODERATE | c.2513A>C | p.Lys838Thr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/31 | 2680/4074 | 2513/3030 | 838/1009 | chr8 | 27451068 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:27397611
|
T | C | 11 | a0001c0009a0001c0012a0001c0021others(8): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
synonymous_variant | LOW | c.27T>C | p.Ser9Ser | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/31 | 194/4074 | 27/3030 | 9/1009 | chr8 | 27397611 | ||
| chr8:27397629
|
G | A | 9 | a0001c0009a0001c0012a0002c0003others(6): Show | 106 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
synonymous_variant | LOW | c.45G>A | p.Thr15Thr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/31 | 212/4074 | 45/3030 | 15/1009 | chr8 | 27397629 | ||
| chr8:27397740
|
T | C | 1 | a0002c0017 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.156T>C | p.Pro52Pro | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/31 | 323/4074 | 156/3030 | 52/1009 | chr8 | 27397740 | ||
| chr8:27397746
|
A | G | 11 | a0001c0009a0001c0012a0001c0021others(8): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
synonymous_variant | LOW | c.162A>G | p.Lys54Lys | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/31 | 329/4074 | 162/3030 | 54/1009 | chr8 | 27397746 | ||
| chr8:27419933
|
G | A | 1 | a0002c0023 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.243G>A | p.Gly81Gly | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/31 | 410/4074 | 243/3030 | 81/1009 | chr8 | 27419933 | ||
| chr8:27420020
|
G | A | 11 | a0001c0001a0001c0013a0001c0021others(8): Show | 100 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
synonymous_variant | LOW | c.330G>A | p.Thr110Thr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/31 | 497/4074 | 330/3030 | 110/1009 | chr8 | 27420020 | ||
| chr8:27422366
|
G | A | 1 | a0001c0013 | 3 | HG00639.hp1 HG02723.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.534G>A | p.Leu178Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/31 | 701/4074 | 534/3030 | 178/1009 | chr8 | 27422366 | ||
| chr8:27431436
|
T | C | 1 | a0002c0024 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.849T>C | p.Pro283Pro | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/31 | 1016/4074 | 849/3030 | 283/1009 | chr8 | 27431436 | ||
| chr8:27435789
|
C | T | 2 | a0001c0010a0010c0032 | 9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
synonymous_variant | LOW | c.1239C>T | p.Pro413Pro | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 14/31 | 1406/4074 | 1239/3030 | 413/1009 | chr8 | 27435789 | ||
| chr8:27436348
|
C | T | 7 | a0001c0001a0001c0007a0001c0012others(4): Show | 90 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
splice_region_variant&synonymous_variant | LOW | c.1341C>T | p.His447His | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/31 | 1508/4074 | 1341/3030 | 447/1009 | chr8 | 27436348 | ||
| chr8:27440238
|
C | T | 1 | a0001c0027 | 1 | HG03098.hp1 | splice_region_variant&synonymous_variant | LOW | c.1836C>T | p.Ala612Ala | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2003/4074 | 1836/3030 | 612/1009 | chr8 | 27440238 | ||
| chr8:27440241
|
G | T | 1 | a0008c0020 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1839G>T | p.Val613Val | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2006/4074 | 1839/3030 | 613/1009 | chr8 | 27440241 | ||
| chr8:27440253
|
G | A | 1 | a0008c0020 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1851G>A | p.Glu617Glu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2018/4074 | 1851/3030 | 617/1009 | chr8 | 27440253 | ||
| chr8:27440289
|
G | A | 1 | a0008c0020 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1887G>A | p.Leu629Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2054/4074 | 1887/3030 | 629/1009 | chr8 | 27440289 | ||
| chr8:27440292
|
G | A | 1 | a0008c0020 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1890G>A | p.Glu630Glu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2057/4074 | 1890/3030 | 630/1009 | chr8 | 27440292 | ||
| chr8:27440307
|
C | A | 1 | a0008c0020 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1905C>A | p.Ile635Ile | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2072/4074 | 1905/3030 | 635/1009 | chr8 | 27440307 | ||
| chr8:27440310
|
G | C | 1 | a0008c0020 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1908G>C | p.Gly636Gly | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2075/4074 | 1908/3030 | 636/1009 | chr8 | 27440310 | ||
| chr8:27444208
|
C | G | 7 | a0002c0004a0002c0018a0002c0026others(4): Show | 37 | HG00438.hp2 HG00621.hp2 HG00741.hp2 others(34): Show |
splice_region_variant&synonymous_variant | LOW | c.2151C>G | p.Pro717Pro | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/31 | 2318/4074 | 2151/3030 | 717/1009 | chr8 | 27444208 | ||
| chr8:27454186
|
T | C | 26 | a0001c0001a0001c0007a0001c0008others(23): Show | 248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
synonymous_variant | LOW | c.2628T>C | p.Thr876Thr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 29/31 | 2795/4074 | 2628/3030 | 876/1009 | chr8 | 27454186 | ||
| chr8:27458359
|
A | G | 25 | a0001c0001a0001c0007a0001c0008others(22): Show | 247 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(244): Show |
synonymous_variant | LOW | c.2880A>G | p.Ala960Ala | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 31/31 | 3047/4074 | 2880/3030 | 960/1009 | chr8 | 27458359 | ||
| chr8:27458383
|
A | G | 24 | a0001c0001a0001c0007a0001c0008others(21): Show | 246 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(243): Show |
synonymous_variant | LOW | c.2904A>G | p.Leu968Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 31/31 | 3071/4074 | 2904/3030 | 968/1009 | chr8 | 27458383 | ||
| chr8:27458419
|
A | G | 1 | a0001c0011 | 6 | HG01192.hp1 HG02056.hp2 NA18949.hp1 others(3): Show |
synonymous_variant | LOW | c.2940A>G | p.Ser980Ser | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 31/31 | 3107/4074 | 2940/3030 | 980/1009 | chr8 | 27458419 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:27325582
|
T | C | 1 | a0001c0001t0005 | 1 | HG01069.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-137T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/31 | chr8 | 27325582 | ||||||
| chr8:27397563
|
A | G | 15 | a0001c0009t0002a0001c0012t0004a0001c0021t0004others(12): Show | 110 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
5_prime_UTR_variant | MODIFIER | c.-22A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/31 | 22 | chr8 | 27397563 | |||||
| chr8:27458600
|
G | A | 12 | a0001c0001t0003a0001c0001t0005a0001c0007t0003others(9): Show | 109 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*91G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 31/31 | 91 | chr8 | 27458600 | |||||
| chr8:27458772
|
G | T | 1 | a0002c0003t0006 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*263G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 31/31 | 263 | chr8 | 27458772 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:27325768
|
C | G | 3 | a0001c0001t0003g0322a0002c0003t0002g0321a0002c0006t0001g0323 | 3 | HG02109.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-38+87C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27325768 | ||||||
| chr8:27325983
|
G | A | 1 | a0001c0002t0001g0005 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-38+302G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27325983 | ||||||
| chr8:27326044
|
A | G | 2 | a0001c0008t0003g0319a0001c0008t0003g0320 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-38+363A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326044 | ||||||
| chr8:27326056
|
C | T | 2 | a0001c0001t0003g0318a0002c0006t0002g0317 | 2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+375C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326056 | ||||||
| chr8:27326057
|
G | T | 6 | a0001c0001t0003g0322a0001c0008t0003g0314a0001c0008t0003g0315others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+376G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326057 | ||||||
| chr8:27326061
|
C | G | 6 | a0001c0001t0003g0322a0001c0008t0003g0314a0001c0008t0003g0315others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+380C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326061 | ||||||
| chr8:27326085
|
C | T | 4 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(1): Show | 4 | HG02056.hp1 NA18943.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+404C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326085 | ||||||
| chr8:27326102
|
G | A | 17 | a0001c0002t0001g0312a0001c0008t0003g0314a0001c0008t0003g0315others(14): Show | 19 | HG00738.hp1 HG02056.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-38+421G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326102 | ||||||
| chr8:27326112
|
C | T | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-38+431C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326112 | ||||||
| chr8:27326193
|
A | G | 110 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0273others(107): Show | 114 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-38+512A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326193 | ||||||
| chr8:27326226
|
A | ATATG | 10 | a0001c0002t0001g0214a0002c0003t0002g0216a0002c0003t0002g0217others(7): Show | 10 | HG00673.hp2 HG02015.hp1 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38+546_-38+547ins others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27326226 | |||||
| chr8:27326226
|
A | ATG | 12 | a0001c0002t0001g0212a0001c0008t0003g0315a0001c0008t0003g0316others(9): Show | 12 | HG01175.hp2 HG02071.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-38+579_-38+580dup others(2): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27326226 | |||||
| chr8:27326226
|
ATG | A | 81 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0024others(78): Show | 83 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.-38+579_-38+580del others(2): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27326226 | |||||
| chr8:27326226
|
ATGTG | A | 22 | a0001c0001t0003g0294a0001c0001t0003g0305a0001c0001t0003g0322others(19): Show | 22 | HG00639.hp1 HG01255.hp1 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.-38+577_-38+580del others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27326226 | |||||
| chr8:27326226
|
ATGTGTG | A | 73 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(70): Show | 75 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-38+575_-38+580del others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27326226 | |||||
| chr8:27326226
|
ATGTGTGT others(3): Show |
A | 2 | a0002c0004t0002g0224a0002c0004t0002g0225 | 2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-38+571_-38+580del others(10): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27326226 | |||||
| chr8:27326277
|
T | C | 100 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0273others(97): Show | 102 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.-38+596T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326277 | ||||||
| chr8:27326709
|
A | G | 2 | a0001c0010t0003g0285a0010c0032t0003g0284 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-38+1028A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326709 | ||||||
| chr8:27326824
|
C | T | 84 | a0001c0001t0003g0088a0001c0001t0003g0273a0001c0001t0003g0276others(81): Show | 86 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-38+1143C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326824 | ||||||
| chr8:27326989
|
G | A | 4 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0002t0001g0226others(1): Show | 4 | HG02572.hp2 HG02818.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+1308G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326989 | ||||||
| chr8:27327060
|
G | A | 70 | a0001c0001t0003g0088a0001c0001t0003g0273a0001c0001t0003g0276others(67): Show | 72 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38+1379G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327060 | ||||||
| chr8:27327178
|
G | A | 70 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(67): Show | 70 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-38+1497G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327178 | ||||||
| chr8:27327203
|
G | A | 1 | a0002c0003t0002g0236 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-38+1522G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327203 | ||||||
| chr8:27327211
|
G | T | 1 | a0001c0002t0001g0206 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-38+1530G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327211 | ||||||
| chr8:27327212
|
C | T | 9 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38+1531C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327212 | ||||||
| chr8:27327380
|
C | A | 4 | a0001c0008t0003g0292a0001c0010t0003g0289a0002c0006t0001g0290others(1): Show | 4 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+1699C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327380 | ||||||
| chr8:27327410
|
GT | G | 69 | a0001c0001t0003g0088a0001c0001t0003g0273a0001c0001t0003g0276others(66): Show | 71 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.-38+1739delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27327410 | |||||
| chr8:27327568
|
A | C | 2 | a0001c0008t0003g0319a0001c0008t0003g0320 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-38+1887A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327568 | ||||||
| chr8:27327649
|
G | A | 1 | a0001c0009t0002g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-38+1968G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327649 | ||||||
| chr8:27327788
|
C | A | 25 | a0001c0001t0003g0095a0001c0001t0003g0096a0001c0001t0003g0097others(22): Show | 25 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.-38+2107C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327788 | ||||||
| chr8:27327863
|
T | A | 1 | a0002c0026t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-38+2182T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327863 | ||||||
| chr8:27327951
|
A | G | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-38+2270A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327951 | ||||||
| chr8:27328050
|
G | A | 7 | a0001c0001t0003g0294a0001c0001t0003g0305a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+2369G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27328050 | ||||||
| chr8:27328411
|
A | G | 2 | a0001c0010t0003g0285a0010c0032t0003g0284 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-38+2730A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27328411 | ||||||
| chr8:27328509
|
T | C | 76 | a0001c0001t0003g0088a0001c0001t0003g0273a0001c0001t0003g0276others(73): Show | 78 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-38+2828T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27328509 | ||||||
| chr8:27328561
|
G | C | 1 | a0002c0004t0002g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-38+2880G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27328561 | ||||||
| chr8:27328934
|
C | T | 187 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(184): Show | 191 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.-38+3253C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27328934 | ||||||
| chr8:27328942
|
C | CTT | 83 | a0001c0001t0003g0088a0001c0001t0003g0273a0001c0001t0003g0276others(80): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-38+3273_-38+3274d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27328942 | |||||
| chr8:27329000
|
C | T | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+3319C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329000 | ||||||
| chr8:27329075
|
T | C | 160 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(157): Show | 162 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-38+3394T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329075 | ||||||
| chr8:27329135
|
G | A | 85 | a0001c0001t0003g0088a0001c0001t0003g0273a0001c0001t0003g0276others(82): Show | 87 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-38+3454G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329135 | ||||||
| chr8:27329191
|
C | T | 19 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0002t0001g0226others(16): Show | 19 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.-38+3510C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329191 | ||||||
| chr8:27329204
|
A | G | 75 | a0001c0001t0003g0088a0001c0001t0003g0273a0001c0001t0003g0276others(72): Show | 77 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-38+3523A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329204 | ||||||
| chr8:27329206
|
G | A | 3 | a0002c0003t0002g0239a0002c0003t0002g0240a0002c0003t0002g0241 | 3 | HG00408.hp2 NA18947.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-38+3525G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329206 | ||||||
| chr8:27329228
|
G | A | 10 | a0001c0001t0003g0294a0001c0001t0003g0305a0001c0007t0003g0303others(7): Show | 10 | HG00639.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38+3547G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329228 | ||||||
| chr8:27329306
|
C | G | 25 | a0001c0001t0003g0095a0001c0001t0003g0096a0001c0001t0003g0097others(22): Show | 25 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.-38+3625C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329306 | ||||||
| chr8:27329339
|
A | G | 1 | a0002c0006t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-38+3658A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329339 | ||||||
| chr8:27329403
|
T | C | 1 | a0002c0006t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-38+3722T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329403 | ||||||
| chr8:27329406
|
A | G | 209 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(206): Show | 214 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.-38+3725A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329406 | ||||||
| chr8:27329667
|
T | C | 5 | a0001c0001t0003g0113a0001c0001t0003g0115a0001c0008t0003g0114others(2): Show | 5 | HG00738.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+3986T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329667 | ||||||
| chr8:27329668
|
T | C | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-38+3987T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329668 | ||||||
| chr8:27329842
|
G | T | 1 | a0001c0002t0001g0190 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-38+4161G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329842 | ||||||
| chr8:27329864
|
A | G | 1 | a0002c0018t0002g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-38+4183A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329864 | ||||||
| chr8:27329899
|
G | T | 1 | a0001c0001t0003g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-38+4218G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329899 | ||||||
| chr8:27329987
|
C | G | 1 | a0001c0007t0003g0189 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-38+4306C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329987 | ||||||
| chr8:27330126
|
C | T | 1 | a0001c0008t0003g0320 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-38+4445C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330126 | ||||||
| chr8:27330136
|
A | G | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+4455A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330136 | ||||||
| chr8:27330153
|
G | A | 1 | a0001c0001t0003g0021 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-38+4472G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330153 | ||||||
| chr8:27330334
|
G | T | 1 | a0002c0006t0001g0287 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-38+4653G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330334 | ||||||
| chr8:27330504
|
C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+4823C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330504 | ||||||
| chr8:27330805
|
G | A | 4 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+5124G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330805 | ||||||
| chr8:27330838
|
G | T | 1 | a0001c0002t0001g0188 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-38+5157G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330838 | ||||||
| chr8:27330968
|
G | A | 1 | a0002c0004t0002g0242 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-38+5287G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330968 | ||||||
| chr8:27330985
|
G | A | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+5304G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330985 | ||||||
| chr8:27331001
|
G | A | 198 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(195): Show | 203 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.-38+5320G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331001 | ||||||
| chr8:27331121
|
C | T | 1 | a0002c0004t0002g0112 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-38+5440C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331121 | ||||||
| chr8:27331141
|
G | A | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | NA18956.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-38+5460G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331141 | ||||||
| chr8:27331287
|
G | A | 5 | a0001c0002t0001g0077a0001c0002t0001g0119a0001c0002t0001g0120others(2): Show | 5 | NA18945.hp2 NA18957.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+5606G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331287 | ||||||
| chr8:27331463
|
T | C | 206 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(203): Show | 211 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.-38+5782T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331463 | ||||||
| chr8:27331476
|
C | CT | 170 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(167): Show | 173 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.-38+5802dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27331476 | |||||
| chr8:27331541
|
C | T | 4 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(1): Show | 4 | HG00544.hp1 HG00609.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+5860C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331541 | ||||||
| chr8:27331640
|
C | T | 1 | a0001c0001t0003g0205 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-38+5959C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331640 | ||||||
| chr8:27331696
|
AG | A | 107 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(104): Show | 108 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.-38+6017delG | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27331696 | |||||
| chr8:27331791
|
T | C | 17 | a0001c0001t0003g0294a0001c0001t0003g0305a0001c0002t0001g0296others(14): Show | 17 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-38+6110T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331791 | ||||||
| chr8:27331844
|
T | C | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-38+6163T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331844 | ||||||
| chr8:27332081
|
C | G | 11 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(8): Show | 13 | HG02056.hp1 HG02622.hp1 NA18943.hp2 others(10): Show |
intron_variant | MODIFIER | c.-38+6400C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332081 | ||||||
| chr8:27332454
|
A | T | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-38+6773A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332454 | ||||||
| chr8:27332535
|
C | T | 2 | a0001c0001t0003g0115a0002c0006t0002g0317 | 2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+6854C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332535 | ||||||
| chr8:27332578
|
A | AT | 20 | a0001c0001t0003g0276a0001c0001t0003g0322a0001c0002t0001g0235others(17): Show | 22 | HG01070.hp2 HG01071.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-38+6908dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27332578 | |||||
| chr8:27332578
|
A | G | 1 | a0002c0003t0002g0275 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-38+6897A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332578 | ||||||
| chr8:27332599
|
C | T | 1 | a0002c0003t0002g0274 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-38+6918C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332599 | ||||||
| chr8:27332658
|
A | T | 204 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(201): Show | 209 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.-38+6977A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332658 | ||||||
| chr8:27332796
|
G | T | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-38+7115G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332796 | ||||||
| chr8:27332864
|
C | A | 1 | a0001c0002t0001g0124 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-38+7183C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332864 | ||||||
| chr8:27332883
|
A | G | 12 | a0001c0001t0003g0322a0001c0002t0001g0235a0001c0002t0001g0312others(9): Show | 14 | HG02056.hp1 HG02109.hp1 HG03471.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+7202A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332883 | ||||||
| chr8:27332908
|
C | T | 1 | a0002c0003t0002g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-38+7227C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332908 | ||||||
| chr8:27332981
|
T | C | 19 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0002t0001g0296others(16): Show | 19 | HG00639.hp1 HG00733.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-38+7300T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332981 | ||||||
| chr8:27333115
|
G | T | 2 | a0001c0008t0003g0114a0002c0006t0001g0010 | 2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+7434G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333115 | ||||||
| chr8:27333182
|
A | G | 2 | a0001c0010t0003g0289a0002c0006t0001g0006 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+7501A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333182 | ||||||
| chr8:27333376
|
G | A | 1 | a0002c0003t0002g0023 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-38+7695G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333376 | ||||||
| chr8:27333386
|
C | T | 12 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(9): Show | 12 | HG00639.hp1 HG00733.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-38+7705C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333386 | ||||||
| chr8:27333428
|
G | A | 11 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0027others(8): Show | 11 | HG01074.hp1 HG01255.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+7747G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333428 | ||||||
| chr8:27333493
|
T | G | 18 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0002t0001g0296others(15): Show | 18 | HG00639.hp1 HG00733.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-38+7812T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333493 | ||||||
| chr8:27333661
|
A | G | 1 | a0002c0006t0001g0068 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-38+7980A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333661 | ||||||
| chr8:27333839
|
G | A | 2 | a0001c0008t0003g0114a0002c0006t0001g0010 | 2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+8158G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333839 | ||||||
| chr8:27334006
|
G | A | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-38+8325G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27334006 | ||||||
| chr8:27334252
|
T | C | 32 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0001t0003g0322others(29): Show | 34 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-38+8571T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27334252 | ||||||
| chr8:27334436
|
C | T | 2 | a0001c0001t0003g0186a0001c0001t0003g0187 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-38+8755C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27334436 | ||||||
| chr8:27334581
|
C | T | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-38+8900C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27334581 | ||||||
| chr8:27334625
|
G | A | 1 | a0001c0009t0002g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-38+8944G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27334625 | ||||||
| chr8:27334719
|
G | A | 182 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(179): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.-38+9038G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27334719 | ||||||
| chr8:27335139
|
A | G | 1 | a0002c0003t0002g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-38+9458A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335139 | ||||||
| chr8:27335197
|
C | T | 10 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38+9516C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335197 | ||||||
| chr8:27335218
|
C | T | 1 | a0001c0001t0003g0034 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-38+9537C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335218 | ||||||
| chr8:27335409
|
A | G | 2 | a0001c0001t0003g0322a0001c0002t0001g0235 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-38+9728A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335409 | ||||||
| chr8:27335595
|
C | CA | 9 | a0001c0001t0003g0322a0001c0002t0001g0235a0001c0008t0003g0114others(6): Show | 9 | HG00738.hp1 HG02109.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-38+9933dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27335595 | |||||
| chr8:27335595
|
CA | C | 25 | a0001c0001t0003g0017a0001c0001t0003g0178a0001c0001t0003g0273others(22): Show | 25 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.-38+9933delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27335595 | |||||
| chr8:27335658
|
C | T | 1 | a0002c0003t0002g0241 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-38+9977C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335658 | ||||||
| chr8:27335660
|
C | T | 1 | a0002c0006t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-38+9979C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335660 | ||||||
| chr8:27335922
|
T | C | 3 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0205 | 3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-38+10241T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335922 | ||||||
| chr8:27335936
|
C | T | 22 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0196others(19): Show | 23 | HG00408.hp1 HG00639.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-38+10255C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335936 | ||||||
| chr8:27335977
|
C | T | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+10296C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335977 | ||||||
| chr8:27336006
|
C | T | 1 | a0002c0003t0004g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-38+10325C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336006 | ||||||
| chr8:27336049
|
G | A | 182 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(179): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.-38+10368G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336049 | ||||||
| chr8:27336138
|
A | G | 1 | a0002c0003t0002g0271 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-38+10457A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336138 | ||||||
| chr8:27336216
|
C | T | 3 | a0001c0009t0002g0237a0002c0003t0002g0270a0002c0003t0002g0274 | 3 | HG00423.hp1 HG02080.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-38+10535C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336216 | ||||||
| chr8:27336290
|
C | T | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+10609C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336290 | ||||||
| chr8:27336406
|
G | T | 182 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(179): Show | 185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.-38+10725G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336406 | ||||||
| chr8:27336490
|
T | C | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+10809T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336490 | ||||||
| chr8:27336534
|
TA | T | 15 | a0001c0001t0003g0322a0001c0002t0001g0235a0001c0002t0001g0312others(12): Show | 17 | HG00738.hp1 HG02056.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-38+10862delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27336534 | |||||
| chr8:27336562
|
T | C | 12 | a0001c0001t0003g0322a0001c0002t0001g0235a0001c0002t0001g0312others(9): Show | 14 | HG02056.hp1 HG02109.hp1 HG03471.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+10881T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336562 | ||||||
| chr8:27336563
|
ATGTAAAC others(2): Show |
A | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+10887_-38+1089 others(13): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27336563 | |||||
| chr8:27336598
|
T | C | 1 | a0002c0004t0002g0011 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-38+10917T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336598 | ||||||
| chr8:27336858
|
C | T | 2 | a0001c0001t0003g0059a0001c0001t0005g0060 | 2 | HG01069.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-38+11177C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336858 | ||||||
| chr8:27336862
|
GTCTC | G | 12 | a0001c0001t0003g0322a0001c0002t0001g0235a0001c0002t0001g0312others(9): Show | 14 | HG02056.hp1 HG02109.hp1 HG03471.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+11187_-38+1119 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27336862 | |||||
| chr8:27336939
|
G | A | 1 | a0002c0003t0002g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-38+11258G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336939 | ||||||
| chr8:27336950
|
C | T | 2 | a0001c0008t0003g0319a0001c0008t0003g0320 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-38+11269C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336950 | ||||||
| chr8:27336992
|
A | G | 214 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(211): Show | 219 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-38+11311A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336992 | ||||||
| chr8:27337112
|
C | T | 189 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(186): Show | 192 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.-38+11431C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337112 | ||||||
| chr8:27337271
|
A | G | 211 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(208): Show | 216 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-38+11590A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337271 | ||||||
| chr8:27337288
|
A | G | 1 | a0002c0003t0002g0069 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-38+11607A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337288 | ||||||
| chr8:27337297
|
G | A | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+11616G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337297 | ||||||
| chr8:27337343
|
G | A | 1 | a0001c0001t0003g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-38+11662G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337343 | ||||||
| chr8:27337364
|
T | C | 10 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(7): Show | 12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+11683T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337364 | ||||||
| chr8:27337528
|
C | T | 1 | a0002c0003t0004g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-38+11847C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337528 | ||||||
| chr8:27337591
|
A | G | 1 | a0002c0005t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-38+11910A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337591 | ||||||
| chr8:27337604
|
T | C | 84 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(81): Show | 85 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-38+11923T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337604 | ||||||
| chr8:27337623
|
G | A | 1 | a0002c0003t0002g0012 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-38+11942G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337623 | ||||||
| chr8:27337760
|
C | G | 1 | a0002c0005t0001g0033 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-38+12079C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337760 | ||||||
| chr8:27337766
|
A | C | 9 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(6): Show | 9 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38+12085A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337766 | ||||||
| chr8:27337851
|
CAT | C | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+12173_-38+1217 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27337851 | |||||
| chr8:27337897
|
C | T | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-38+12216C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337897 | ||||||
| chr8:27338044
|
C | T | 10 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(7): Show | 12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+12363C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338044 | ||||||
| chr8:27338045
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-38+12364G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338045 | ||||||
| chr8:27338046
|
T | A | 31 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0002t0001g0296others(28): Show | 33 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-38+12365T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338046 | ||||||
| chr8:27338068
|
T | C | 10 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(7): Show | 12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+12387T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338068 | ||||||
| chr8:27338201
|
G | A | 1 | a0001c0001t0003g0276 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-38+12520G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338201 | ||||||
| chr8:27338455
|
G | A | 2 | a0002c0004t0002g0244a0002c0004t0002g0245 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-38+12774G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338455 | ||||||
| chr8:27338651
|
A | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+12970A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338651 | ||||||
| chr8:27338700
|
T | C | 1 | a0001c0001t0003g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-38+13019T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338700 | ||||||
| chr8:27339073
|
G | A | 1 | a0002c0003t0002g0069 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-38+13392G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339073 | ||||||
| chr8:27339191
|
G | T | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+13510G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339191 | ||||||
| chr8:27339278
|
T | G | 1 | a0002c0004t0002g0250 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-38+13597T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339278 | ||||||
| chr8:27339482
|
C | T | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+13801C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339482 | ||||||
| chr8:27339489
|
T | C | 1 | a0002c0003t0002g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-38+13808T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339489 | ||||||
| chr8:27339581
|
A | T | 1 | a0002c0006t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-38+13900A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339581 | ||||||
| chr8:27339663
|
G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-38+13982G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339663 | ||||||
| chr8:27339738
|
A | G | 1 | a0002c0006t0001g0323 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-38+14057A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339738 | ||||||
| chr8:27340071
|
G | A | 5 | a0001c0002t0001g0127a0001c0002t0001g0128a0001c0002t0001g0190others(2): Show | 5 | NA18943.hp1 NA19000.hp1 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+14390G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340071 | ||||||
| chr8:27340098
|
G | C | 2 | a0001c0007t0003g0277a0001c0007t0003g0278 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-38+14417G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340098 | ||||||
| chr8:27340175
|
C | T | 4 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+14494C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340175 | ||||||
| chr8:27340209
|
A | T | 1 | a0001c0011t0001g0098 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-38+14528A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340209 | ||||||
| chr8:27340256
|
G | A | 4 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(1): Show | 4 | HG00544.hp1 HG00609.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+14575G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340256 | ||||||
| chr8:27340362
|
G | A | 1 | a0001c0001t0003g0035 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-38+14681G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340362 | ||||||
| chr8:27340586
|
G | T | 13 | a0001c0002t0001g0312a0001c0008t0003g0114a0001c0009t0002g0310others(10): Show | 15 | HG00738.hp1 HG02056.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38+14905G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340586 | ||||||
| chr8:27340660
|
C | T | 2 | a0001c0008t0003g0114a0002c0006t0001g0010 | 2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+14979C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340660 | ||||||
| chr8:27340668
|
C | G | 1 | a0001c0001t0003g0052 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-38+14987C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340668 | ||||||
| chr8:27340721
|
T | C | 1 | a0001c0002t0001g0129 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-38+15040T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340721 | ||||||
| chr8:27340747
|
C | T | 10 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(7): Show | 12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+15066C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340747 | ||||||
| chr8:27340942
|
A | G | 2 | a0001c0001t0003g0322a0001c0002t0001g0235 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-38+15261A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340942 | ||||||
| chr8:27341053
|
C | T | 1 | a0002c0004t0002g0111 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-38+15372C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341053 | ||||||
| chr8:27341114
|
C | T | 2 | a0001c0001t0003g0322a0001c0002t0001g0235 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-38+15433C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341114 | ||||||
| chr8:27341288
|
G | A | 1 | a0001c0008t0003g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-38+15607G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341288 | ||||||
| chr8:27341367
|
G | A | 199 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(196): Show | 202 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-38+15686G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341367 | ||||||
| chr8:27341380
|
G | A | 1 | a0001c0009t0002g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-38+15699G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341380 | ||||||
| chr8:27341440
|
G | A | 3 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0205 | 3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-38+15759G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341440 | ||||||
| chr8:27341518
|
G | T | 13 | a0001c0002t0001g0312a0001c0008t0003g0114a0001c0009t0002g0310others(10): Show | 15 | HG00738.hp1 HG02056.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38+15837G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341518 | ||||||
| chr8:27341519
|
A | C | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-38+15838A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341519 | ||||||
| chr8:27341664
|
G | A | 7 | a0001c0001t0003g0178a0001c0002t0001g0173a0001c0002t0001g0174others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+15983G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341664 | ||||||
| chr8:27341666
|
G | T | 3 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0205 | 3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-38+15985G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341666 | ||||||
| chr8:27341710
|
G | T | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+16029G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341710 | ||||||
| chr8:27341734
|
C | T | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-38+16053C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341734 | ||||||
| chr8:27341735
|
A | G | 315 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(312): Show | 320 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.-38+16054A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341735 | ||||||
| chr8:27341753
|
A | C | 1 | a0002c0003t0002g0269 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-38+16072A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341753 | ||||||
| chr8:27341928
|
A | G | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-38+16247A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341928 | ||||||
| chr8:27341961
|
A | G | 1 | a0002c0003t0002g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-38+16280A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341961 | ||||||
| chr8:27341991
|
A | T | 13 | a0001c0002t0001g0312a0001c0008t0003g0114a0001c0009t0002g0310others(10): Show | 15 | HG00738.hp1 HG02056.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38+16310A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341991 | ||||||
| chr8:27342021
|
A | G | 2 | a0001c0002t0001g0171a0001c0002t0001g0172 | 2 | NA18981.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-38+16340A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342021 | ||||||
| chr8:27342099
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-38+16418C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342099 | ||||||
| chr8:27342118
|
G | C | 10 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(7): Show | 12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+16437G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342118 | ||||||
| chr8:27342217
|
A | T | 10 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(7): Show | 12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+16536A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342217 | ||||||
| chr8:27342289
|
CT | C | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+16620delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27342289 | |||||
| chr8:27342299
|
T | C | 1 | a0001c0001t0003g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-38+16618T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342299 | ||||||
| chr8:27342302
|
C | G | 1 | a0002c0006t0001g0287 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-38+16621C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342302 | ||||||
| chr8:27342364
|
T | G | 213 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(210): Show | 218 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-38+16683T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342364 | ||||||
| chr8:27342562
|
G | A | 10 | a0001c0002t0001g0127a0001c0002t0001g0128a0001c0002t0001g0138others(7): Show | 10 | HG00735.hp2 HG01993.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38+16881G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342562 | ||||||
| chr8:27342570
|
C | T | 192 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(189): Show | 195 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.-38+16889C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342570 | ||||||
| chr8:27342629
|
C | G | 3 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295 | 3 | HG02109.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-38+16948C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342629 | ||||||
| chr8:27342685
|
G | T | 1 | a0002c0003t0002g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-38+17004G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342685 | ||||||
| chr8:27342759
|
A | T | 1 | a0001c0009t0002g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-38+17078A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342759 | ||||||
| chr8:27342819
|
A | G | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+17138A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342819 | ||||||
| chr8:27342825
|
C | T | 2 | a0001c0008t0003g0319a0001c0008t0003g0320 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-38+17144C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342825 | ||||||
| chr8:27342862
|
T | A | 4 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+17181T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342862 | ||||||
| chr8:27343055
|
T | G | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+17374T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343055 | ||||||
| chr8:27343447
|
G | A | 216 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(213): Show | 221 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.-38+17766G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343447 | ||||||
| chr8:27343563
|
C | T | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+17882C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343563 | ||||||
| chr8:27343564
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-38+17883G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343564 | ||||||
| chr8:27343801
|
A | G | 2 | a0001c0010t0003g0289a0002c0006t0001g0006 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+18120A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343801 | ||||||
| chr8:27343876
|
G | A | 195 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(192): Show | 198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.-38+18195G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343876 | ||||||
| chr8:27343998
|
G | A | 1 | a0001c0007t0003g0279 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-38+18317G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343998 | ||||||
| chr8:27344043
|
T | C | 1 | a0002c0003t0002g0251 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-38+18362T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344043 | ||||||
| chr8:27344137
|
G | A | 1 | a0001c0010t0003g0297 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-38+18456G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344137 | ||||||
| chr8:27344228
|
A | G | 1 | a0002c0003t0002g0223 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-38+18547A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344228 | ||||||
| chr8:27344262
|
C | T | 7 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0183others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+18581C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344262 | ||||||
| chr8:27344275
|
G | A | 1 | a0001c0001t0003g0024 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-38+18594G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344275 | ||||||
| chr8:27344339
|
C | T | 1 | a0001c0013t0003g0304 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-38+18658C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344339 | ||||||
| chr8:27344384
|
C | T | 7 | a0001c0001t0003g0088a0001c0001t0003g0273a0002c0003t0002g0180others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+18703C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344384 | ||||||
| chr8:27344534
|
T | C | 2 | a0001c0010t0003g0289a0002c0006t0001g0006 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+18853T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344534 | ||||||
| chr8:27344688
|
C | G | 1 | a0001c0010t0003g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+19007C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344688 | ||||||
| chr8:27344752
|
G | A | 1 | a0001c0002t0001g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-38+19071G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344752 | ||||||
| chr8:27344757
|
G | T | 1 | a0001c0002t0001g0170 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-38+19076G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344757 | ||||||
| chr8:27344780
|
A | T | 13 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0288others(10): Show | 13 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-38+19099A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344780 | ||||||
| chr8:27344793
|
C | T | 1 | a0002c0003t0002g0265 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-38+19112C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344793 | ||||||
| chr8:27344833
|
C | G | 2 | a0001c0001t0003g0113a0001c0001t0003g0115 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+19152C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344833 | ||||||
| chr8:27344927
|
C | CT | 201 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(198): Show | 204 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.-38+19248dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27344927 | |||||
| chr8:27345110
|
C | T | 10 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(7): Show | 12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+19429C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345110 | ||||||
| chr8:27345187
|
C | T | 10 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(7): Show | 12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+19506C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345187 | ||||||
| chr8:27345290
|
G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-38+19609G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345290 | ||||||
| chr8:27345304
|
A | G | 1 | a0001c0001t0003g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-38+19623A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345304 | ||||||
| chr8:27345519
|
A | G | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+19838A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345519 | ||||||
| chr8:27345522
|
C | T | 254 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(251): Show | 259 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.-38+19841C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345522 | ||||||
| chr8:27345549
|
T | A | 10 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(7): Show | 12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+19868T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345549 | ||||||
| chr8:27345628
|
T | C | 1 | a0001c0002t0001g0192 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-38+19947T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345628 | ||||||
| chr8:27345635
|
A | G | 1 | a0002c0005t0001g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-38+19954A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345635 | ||||||
| chr8:27345640
|
A | G | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+19959A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345640 | ||||||
| chr8:27345666
|
A | G | 1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-38+19985A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345666 | ||||||
| chr8:27345699
|
A | T | 2 | a0001c0010t0003g0289a0002c0006t0001g0006 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+20018A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345699 | ||||||
| chr8:27346125
|
A | G | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+20444A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346125 | ||||||
| chr8:27346336
|
A | T | 1 | a0002c0004t0002g0250 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-38+20655A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346336 | ||||||
| chr8:27346338
|
T | C | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+20657T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346338 | ||||||
| chr8:27346355
|
C | T | 1 | a0002c0005t0001g0202 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-38+20674C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346355 | ||||||
| chr8:27346499
|
T | C | 1 | a0001c0002t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-38+20818T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346499 | ||||||
| chr8:27346605
|
A | G | 2 | a0001c0001t0003g0113a0001c0001t0003g0115 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+20924A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346605 | ||||||
| chr8:27346607
|
G | A | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-38+20926G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346607 | ||||||
| chr8:27346638
|
A | G | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-38+20957A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346638 | ||||||
| chr8:27346767
|
G | A | 1 | a0002c0003t0002g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-38+21086G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346767 | ||||||
| chr8:27347000
|
C | G | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-38+21319C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347000 | ||||||
| chr8:27347081
|
A | G | 70 | a0001c0001t0003g0054a0001c0001t0003g0088a0001c0001t0003g0273others(67): Show | 72 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38+21400A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347081 | ||||||
| chr8:27347146
|
A | G | 200 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(197): Show | 203 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-38+21465A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347146 | ||||||
| chr8:27347214
|
T | TA | 17 | a0001c0001t0003g0178a0001c0001t0003g0322a0001c0002t0001g0173others(14): Show | 17 | HG00738.hp1 HG01169.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-38+21549dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27347214 | |||||
| chr8:27347214
|
T | TAA | 198 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(195): Show | 203 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-38+21548_-38+2154 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27347214 | |||||
| chr8:27347214
|
T | TAAA | 10 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(7): Show | 10 | HG00639.hp1 HG00733.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38+21547_-38+2154 others(7): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27347214 | |||||
| chr8:27347246
|
G | A | 4 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+21565G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347246 | ||||||
| chr8:27347253
|
G | A | 1 | a0001c0001t0003g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-38+21572G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347253 | ||||||
| chr8:27347340
|
A | G | 215 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(212): Show | 220 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.-38+21659A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347340 | ||||||
| chr8:27347529
|
AG | A | 110 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(107): Show | 111 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-38+21850delG | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27347529 | |||||
| chr8:27347718
|
G | A | 14 | a0001c0001t0003g0178a0001c0001t0003g0276a0001c0002t0001g0173others(11): Show | 14 | HG01070.hp2 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-38+22037G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347718 | ||||||
| chr8:27347765
|
A | T | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | NA18956.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-38+22084A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347765 | ||||||
| chr8:27347772
|
C | G | 2 | a0001c0001t0003g0113a0001c0001t0003g0115 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+22091C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347772 | ||||||
| chr8:27347938
|
A | G | 2 | a0001c0007t0003g0277a0001c0007t0003g0278 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-38+22257A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347938 | ||||||
| chr8:27348029
|
G | A | 1 | a0001c0001t0003g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-38+22348G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348029 | ||||||
| chr8:27348177
|
A | G | 1 | a0001c0008t0003g0320 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-38+22496A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348177 | ||||||
| chr8:27348260
|
G | A | 215 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(212): Show | 220 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.-38+22579G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348260 | ||||||
| chr8:27348267
|
G | A | 2 | a0001c0001t0003g0322a0001c0002t0001g0235 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-38+22586G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348267 | ||||||
| chr8:27348279
|
G | C | 3 | a0001c0008t0003g0114a0002c0006t0001g0010a0002c0006t0002g0317 | 3 | HG00738.hp1 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+22598G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348279 | ||||||
| chr8:27348305
|
G | A | 1 | a0001c0010t0003g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-38+22624G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348305 | ||||||
| chr8:27348317
|
G | A | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-38+22636G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348317 | ||||||
| chr8:27348350
|
C | T | 3 | a0001c0008t0003g0114a0002c0006t0001g0010a0002c0006t0002g0317 | 3 | HG00738.hp1 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+22669C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348350 | ||||||
| chr8:27348385
|
A | G | 2 | a0001c0001t0003g0113a0001c0001t0003g0115 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+22704A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348385 | ||||||
| chr8:27348488
|
C | T | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+22807C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348488 | ||||||
| chr8:27348599
|
G | A | 3 | a0001c0008t0003g0114a0002c0006t0001g0010a0002c0006t0002g0317 | 3 | HG00738.hp1 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+22918G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348599 | ||||||
| chr8:27348665
|
C | T | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+22984C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348665 | ||||||
| chr8:27348674
|
A | G | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-38+22993A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348674 | ||||||
| chr8:27348727
|
C | T | 7 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+23046C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348727 | ||||||
| chr8:27348754
|
C | T | 2 | a0002c0003t0002g0004a0002c0003t0002g0264 | 3 | HG01257.hp2 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-38+23073C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348754 | ||||||
| chr8:27348884
|
C | T | 2 | a0001c0010t0003g0289a0002c0006t0001g0006 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+23203C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348884 | ||||||
| chr8:27349095
|
C | A | 10 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(7): Show | 12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+23414C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27349095 | ||||||
| chr8:27349181
|
A | G | 2 | a0002c0004t0002g0109a0002c0004t0002g0110 | 2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-38+23500A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27349181 | ||||||
| chr8:27349380
|
C | T | 1 | a0002c0005t0001g0201 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-38+23699C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27349380 | ||||||
| chr8:27349673
|
A | G | 2 | a0001c0010t0003g0289a0002c0006t0001g0006 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+23992A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27349673 | ||||||
| chr8:27350128
|
A | G | 4 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+24447A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350128 | ||||||
| chr8:27350249
|
G | A | 4 | a0001c0002t0001g0130a0001c0008t0003g0114a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02602.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+24568G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350249 | ||||||
| chr8:27350254
|
G | A | 1 | a0001c0001t0003g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-38+24573G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350254 | ||||||
| chr8:27350378
|
CCCAG | C | 200 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(197): Show | 203 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-38+24702_-38+2470 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350378 | |||||
| chr8:27350548
|
C | G | 1 | a0002c0004t0002g0298 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-38+24867C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350548 | ||||||
| chr8:27350548
|
C | T | 1 | a0001c0002t0001g0169 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-38+24867C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350548 | ||||||
| chr8:27350575
|
G | GCCTCC | 72 | a0001c0001t0003g0054a0001c0001t0003g0088a0001c0001t0003g0273others(69): Show | 74 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-38+24895_-38+2489 others(9): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350575 | |||||
| chr8:27350601
|
C | A | 2 | a0001c0008t0003g0114a0002c0006t0001g0010 | 2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+24920C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350601 | ||||||
| chr8:27350609
|
G | A | 109 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(106): Show | 110 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-38+24928G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350609 | ||||||
| chr8:27350646
|
C | G | 1 | a0001c0002t0001g0192 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-38+24965C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350646 | ||||||
| chr8:27350712
|
C | A | 2 | a0001c0008t0003g0114a0002c0006t0001g0010 | 2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+25031C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350712 | ||||||
| chr8:27350718
|
C | T | 5 | a0001c0002t0001g0168a0001c0002t0001g0296a0001c0008t0003g0243others(2): Show | 5 | HG01496.hp1 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+25037C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350718 | ||||||
| chr8:27350739
|
G | T | 1 | a0001c0002t0001g0138 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-38+25058G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350739 | ||||||
| chr8:27350745
|
G | T | 193 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(190): Show | 196 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.-38+25064G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350745 | ||||||
| chr8:27350775
|
C | CAA | 10 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(7): Show | 12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+25095_-38+2509 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350775 | |||||
| chr8:27350900
|
C | T | 3 | a0001c0008t0003g0114a0002c0006t0001g0010a0002c0006t0002g0317 | 3 | HG00738.hp1 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+25219C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350900 | ||||||
| chr8:27350975
|
C | CA | 6 | a0001c0008t0003g0295a0001c0010t0003g0229a0001c0011t0001g0142others(3): Show | 6 | HG01256.hp2 HG01258.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+25310dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350975
|
C | CAA | 6 | a0001c0001t0003g0050a0001c0002t0001g0175a0001c0002t0001g0176others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+25309_-38+2531 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350975
|
C | CAAAAAAA others(4): Show |
3 | a0001c0002t0001g0296a0001c0010t0003g0231a0001c0010t0003g0233 | 3 | HG02486.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-38+25300_-38+2531 others(15): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350975
|
C | CAAAAAAA others(5): Show |
1 | a0002c0006t0001g0287 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-38+25299_-38+2531 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350975
|
C | CAAAAAAA others(6): Show |
2 | a0001c0010t0003g0232a0002c0005t0001g0002 | 3 | HG00639.hp2 HG01109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-38+25298_-38+2531 others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350975
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0003g0064a0001c0001t0003g0228a0001c0010t0003g0285others(1): Show | 4 | HG02809.hp1 HG02818.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+25297_-38+2531 others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350975
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0003g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-38+25296_-38+2531 others(19): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350975
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0003g0037a0002c0006t0001g0286 | 2 | HG00438.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(22): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350975
|
C | CAAAAAAA others(12): Show |
6 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0075others(3): Show | 6 | HG01099.hp1 HG01169.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(23): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350975
|
C | CAAAAAAA others(13): Show |
4 | a0001c0001t0003g0047a0001c0025t0001g0019a0002c0006t0001g0062others(1): Show | 4 | HG02922.hp1 HG03130.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350975
|
C | CAAAAAAA others(14): Show |
5 | a0001c0001t0003g0021a0001c0001t0003g0034a0001c0001t0003g0039others(2): Show | 5 | HG00621.hp1 HG02004.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(25): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350975
|
C | CAAAAAAA others(15): Show |
5 | a0001c0001t0003g0027a0001c0001t0003g0042a0001c0001t0005g0060others(2): Show | 5 | HG01069.hp1 HG01496.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(26): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350975
|
C | CAAAAAAA others(16): Show |
2 | a0001c0001t0003g0040a0001c0001t0003g0045 | 2 | HG02135.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(27): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350975
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0003g0052 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(28): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | |||||
| chr8:27350988
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-38+25307_-38+2530 others(15): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350988 | ||||||
| chr8:27350988
|
A | ATATATAT others(6): Show |
1 | a0001c0011t0001g0165 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-38+25307_-38+2530 others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350988 | ||||||
| chr8:27350988
|
A | T | 1 | a0001c0002t0001g0167 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-38+25307A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350988 | ||||||
| chr8:27350988
|
AAAATATA others(13): Show |
A | 1 | a0001c0001t0003g0322 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-38+25309_-38+2532 others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350988 | |||||
| chr8:27350989
|
AAATATAT others(4): Show |
A | 2 | a0001c0002t0001g0164a0002c0006t0001g0282 | 2 | NA18978.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-38+25310_-38+2532 others(15): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350989 | |||||
| chr8:27350989
|
AAATATAT others(8): Show |
A | 1 | a0001c0002t0001g0163 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2532 others(19): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350989 | |||||
| chr8:27350989
|
AAATATAT others(10): Show |
A | 5 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(2): Show | 5 | HG00544.hp2 NA18991.hp1 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+25310_-38+2532 others(21): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350989 | |||||
| chr8:27350989
|
AAATATAT others(12): Show |
A | 6 | a0001c0002t0001g0079a0001c0002t0001g0155a0001c0002t0001g0157others(3): Show | 6 | HG01928.hp2 HG02040.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+25310_-38+2532 others(23): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350989 | |||||
| chr8:27350989
|
AAATATAT others(26): Show |
A | 3 | a0001c0002t0001g0005a0001c0002t0001g0129a0007c0029t0001g0153 | 3 | NA18968.hp1 NA18995.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-38+25310_-38+2534 others(37): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350989 | |||||
| chr8:27350989
|
AAATATAT others(30): Show |
A | 1 | a0001c0002t0001g0212 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2534 others(41): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350989 | |||||
| chr8:27350990
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0003g0059 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(36): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(33): Show |
1 | a0002c0006t0001g0038 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(44): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0003g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(23): Show |
2 | a0001c0001t0003g0025a0001c0001t0003g0305 | 2 | HG01074.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(34): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(31): Show |
1 | a0001c0001t0003g0071 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(42): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0003g0046 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(29): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(24): Show |
2 | a0001c0001t0003g0072a0002c0005t0001g0026 | 2 | HG02300.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(35): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0003g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(37): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0003g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(39): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(23): Show |
1 | a0001c0010t0003g0230 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(34): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(32): Show |
1 | a0001c0001t0003g0028 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(43): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(38): Show |
1 | a0001c0001t0003g0029 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(49): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(23): Show |
1 | a0001c0012t0004g0030 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(34): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(22): Show |
1 | a0002c0006t0001g0323 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(33): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0003g0032 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(37): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(28): Show |
1 | a0002c0006t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(39): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(13): Show |
1 | a0001c0002t0001g0116 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(26): Show |
2 | a0002c0005t0001g0033a0002c0026t0001g0238 | 2 | HG01928.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(37): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0318 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(22): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(12): Show |
1 | a0001c0008t0003g0320 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(23): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(9): Show |
1 | a0001c0008t0003g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(22): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0003g0024 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAA others(5): Show |
1 | a0001c0002t0001g0173 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAAAT others(8): Show |
1 | a0001c0002t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(19): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAATA others(7): Show |
1 | a0001c0007t0003g0177 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAAAATA others(9): Show |
1 | a0001c0001t0003g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAAATATA others(5): Show |
1 | a0001c0002t0001g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAATATAT others(10): Show |
1 | a0001c0002t0001g0120 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(21): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAATATAT others(18): Show |
1 | a0001c0002t0001g0121 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(29): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AAATATAT others(20): Show |
1 | a0001c0002t0001g0132 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(31): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AATATATA others(5): Show |
1 | a0001c0007t0003g0137 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-38+25349_-38+2536 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | AATATATA others(7): Show |
1 | a0001c0002t0001g0122 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-38+25347_-38+2536 others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
A | T | 6 | a0001c0002t0001g0077a0001c0002t0001g0080a0001c0002t0001g0118others(3): Show | 6 | HG02071.hp2 HG03710.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+25309A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350990 | ||||||
| chr8:27350990
|
AATAT | A | 7 | a0001c0002t0001g0146a0001c0002t0001g0169a0001c0011t0001g0078others(4): Show | 7 | HG01192.hp1 HG01361.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+25357_-38+2536 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
AATATATA others(1): Show |
A | 8 | a0001c0001t0003g0041a0001c0002t0001g0127a0001c0007t0003g0280others(5): Show | 8 | HG02074.hp1 HG02080.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+25353_-38+2536 others(12): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
AATATATA others(3): Show |
A | 3 | a0001c0002t0001g0214a0001c0012t0004g0211a0002c0004t0002g0109 | 3 | HG01175.hp2 HG03490.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-38+25351_-38+2536 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
AATATATA others(5): Show |
A | 9 | a0001c0001t0003g0095a0001c0009t0002g0103a0001c0009t0002g0106others(6): Show | 9 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38+25349_-38+2536 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
AATATATA others(7): Show |
A | 6 | a0001c0007t0003g0279a0001c0011t0001g0098a0002c0003t0002g0216others(3): Show | 6 | HG03927.hp1 NA18522.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+25347_-38+2536 others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
AATATATA others(9): Show |
A | 14 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0012t0004g0057others(11): Show | 14 | HG00733.hp2 HG01081.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.-38+25345_-38+2536 others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
AATATATA others(11): Show |
A | 8 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(5): Show | 8 | HG01168.hp1 HG01516.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+25343_-38+2536 others(22): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
AATATATA others(13): Show |
A | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-38+25341_-38+2536 others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
AATATATA others(17): Show |
A | 1 | a0002c0003t0002g0264 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-38+25337_-38+2536 others(28): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
AATATATA others(19): Show |
A | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+25335_-38+2536 others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350990
|
AATATATA others(21): Show |
A | 2 | a0001c0008t0003g0114a0002c0006t0001g0010 | 2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+25333_-38+2536 others(32): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | |||||
| chr8:27350991
|
AT | A | 12 | a0001c0001t0003g0082a0001c0002t0001g0138a0001c0002t0001g0170others(9): Show | 12 | HG00609.hp2 HG00735.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+25311delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | ||||||
| chr8:27350991
|
ATAT | A | 8 | a0001c0001t0003g0294a0001c0002t0001g0139a0001c0002t0001g0190others(5): Show | 8 | HG00639.hp1 HG02135.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+25311_-38+2531 others(7): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | ||||||
| chr8:27350991
|
ATATAT | A | 4 | a0001c0001t0003g0182a0001c0001t0003g0187a0001c0002t0001g0206others(1): Show | 4 | HG00741.hp2 HG02257.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+25311_-38+2531 others(9): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | ||||||
| chr8:27350991
|
ATATATAT others(4): Show |
A | 2 | a0002c0004t0002g0110a0002c0004t0002g0141 | 2 | HG03704.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-38+25311_-38+2532 others(15): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | ||||||
| chr8:27350991
|
ATATATAT others(6): Show |
A | 10 | a0001c0001t0003g0096a0001c0001t0003g0097a0002c0003t0002g0055others(7): Show | 10 | HG00323.hp2 HG01106.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38+25311_-38+2532 others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | ||||||
| chr8:27350991
|
ATATATAT others(8): Show |
A | 29 | a0001c0001t0003g0054a0001c0001t0003g0276a0001c0002t0001g0140others(26): Show | 30 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.-38+25311_-38+2532 others(19): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | ||||||
| chr8:27350991
|
ATATATAT others(10): Show |
A | 16 | a0001c0001t0003g0143a0001c0001t0003g0184a0001c0001t0003g0273others(13): Show | 16 | HG00408.hp2 HG00673.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-38+25311_-38+2532 others(21): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | ||||||
| chr8:27350991
|
ATATATAT others(12): Show |
A | 2 | a0001c0001t0003g0185a0002c0003t0002g0268 | 2 | HG03540.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-38+25311_-38+2532 others(23): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | ||||||
| chr8:27350991
|
ATATATAT others(16): Show |
A | 2 | a0002c0003t0002g0004a0002c0003t0002g0207 | 3 | HG01258.hp1 HG01361.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-38+25311_-38+2533 others(27): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | ||||||
| chr8:27350991
|
ATATATAT others(18): Show |
A | 8 | a0001c0002t0001g0312a0001c0009t0002g0313a0002c0003t0002g0012others(5): Show | 10 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38+25311_-38+2533 others(29): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | ||||||
| chr8:27350991
|
ATATATAT others(20): Show |
A | 1 | a0002c0006t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-38+25311_-38+2533 others(31): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | ||||||
| chr8:27350991
|
ATATATAT others(22): Show |
A | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+25311_-38+2533 others(33): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | ||||||
| chr8:27350991
|
ATATATAT others(30): Show |
A | 1 | a0001c0002t0001g0119 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-38+25311_-38+2534 others(41): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | ||||||
| chr8:27350992
|
T | A | 70 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0034others(67): Show | 71 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.-38+25311T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350992 | ||||||
| chr8:27350994
|
T | A | 70 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0022others(67): Show | 71 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.-38+25313T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350994 | ||||||
| chr8:27350996
|
T | A | 69 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0022others(66): Show | 70 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.-38+25315T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350996 | ||||||
| chr8:27350998
|
T | A | 65 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0022others(62): Show | 65 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.-38+25317T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350998 | ||||||
| chr8:27351000
|
T | A | 63 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0022others(60): Show | 63 | HG00609.hp1 HG00639.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-38+25319T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351000 | ||||||
| chr8:27351002
|
T | A | 58 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0022others(55): Show | 58 | HG00609.hp1 HG00639.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.-38+25321T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351002 | ||||||
| chr8:27351004
|
T | A | 58 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0035others(55): Show | 58 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-38+25323T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351004 | ||||||
| chr8:27351006
|
T | A | 54 | a0001c0001t0003g0016a0001c0001t0003g0035a0001c0001t0003g0041others(51): Show | 54 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-38+25325T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351006 | ||||||
| chr8:27351008
|
T | A | 78 | a0001c0001t0003g0016a0001c0001t0003g0035a0001c0001t0003g0041others(75): Show | 79 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-38+25327T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351008 | ||||||
| chr8:27351010
|
T | A | 89 | a0001c0001t0003g0035a0001c0001t0003g0041a0001c0001t0003g0054others(86): Show | 90 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-38+25329T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351010 | ||||||
| chr8:27351012
|
T | A | 83 | a0001c0001t0003g0035a0001c0001t0003g0041a0001c0001t0003g0054others(80): Show | 84 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.-38+25331T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351012 | ||||||
| chr8:27351014
|
T | A | 75 | a0001c0001t0003g0035a0001c0001t0003g0041a0001c0001t0003g0054others(72): Show | 76 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.-38+25333T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351014 | ||||||
| chr8:27351016
|
T | A | 64 | a0001c0001t0003g0041a0001c0001t0003g0054a0001c0001t0003g0088others(61): Show | 65 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-38+25335T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351016 | ||||||
| chr8:27351016
|
TATATATA others(19): Show |
T | 1 | a0002c0004t0002g0191 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-38+25336_-38+2536 others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351016 | ||||||
| chr8:27351018
|
T | A | 43 | a0001c0001t0003g0041a0001c0001t0003g0095a0001c0001t0003g0096others(40): Show | 46 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.-38+25337T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351018 | ||||||
| chr8:27351018
|
TATATATA others(17): Show |
T | 1 | a0001c0009t0002g0310 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-38+25338_-38+2536 others(28): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351018 | ||||||
| chr8:27351020
|
T | A | 23 | a0001c0001t0003g0041a0001c0001t0003g0095a0001c0001t0003g0096others(20): Show | 25 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-38+25339T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351020 | ||||||
| chr8:27351022
|
T | A | 20 | a0001c0001t0003g0041a0001c0001t0003g0095a0001c0001t0003g0096others(17): Show | 22 | HG00323.hp2 HG00738.hp1 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.-38+25341T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351022 | ||||||
| chr8:27351024
|
T | A | 14 | a0001c0001t0003g0113a0001c0001t0003g0115a0001c0002t0001g0312others(11): Show | 16 | HG00738.hp1 HG02056.hp1 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.-38+25343T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351024 | ||||||
| chr8:27351026
|
T | A | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+25345T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351026 | ||||||
| chr8:27351032
|
TATATATA others(3): Show |
T | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+25352_-38+2536 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351032 | ||||||
| chr8:27351038
|
TATAC | T | 4 | a0001c0001t0003g0016a0001c0001t0003g0181a0001c0001t0003g0183others(1): Show | 4 | HG02970.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+25358_-38+2536 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351038 | ||||||
| chr8:27351040
|
T | C | 10 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(7): Show | 10 | HG00639.hp1 HG00733.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38+25359T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351040 | ||||||
| chr8:27351042
|
C | T | 18 | a0001c0001t0003g0182a0001c0001t0003g0184a0001c0001t0003g0185others(15): Show | 20 | HG00609.hp1 HG02055.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.-38+25361C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351042 | ||||||
| chr8:27351247
|
T | C | 4 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+25566T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351247 | ||||||
| chr8:27351315
|
A | G | 3 | a0001c0001t0003g0095a0001c0001t0003g0096a0001c0001t0003g0097 | 3 | HG00323.hp2 HG01515.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-38+25634A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351315 | ||||||
| chr8:27351604
|
T | A | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+25923T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351604 | ||||||
| chr8:27351731
|
A | C | 3 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0205 | 3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-38+26050A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351731 | ||||||
| chr8:27351738
|
T | G | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+26057T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351738 | ||||||
| chr8:27352033
|
G | A | 2 | a0002c0003t0002g0249a0002c0017t0002g0252 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-38+26352G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352033 | ||||||
| chr8:27352069
|
C | A | 6 | a0002c0005t0001g0083a0002c0005t0001g0084a0002c0005t0001g0085others(3): Show | 6 | NA18970.hp1 NA18979.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+26388C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352069 | ||||||
| chr8:27352080
|
CAG | C | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+26400_-38+2640 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352080 | ||||||
| chr8:27352095
|
G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-38+26414G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352095 | ||||||
| chr8:27352230
|
T | G | 1 | a0002c0005t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-38+26549T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352230 | ||||||
| chr8:27352373
|
A | G | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+26692A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352373 | ||||||
| chr8:27352414
|
C | T | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-38+26733C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352414 | ||||||
| chr8:27352573
|
A | C | 4 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+26892A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352573 | ||||||
| chr8:27352638
|
G | A | 1 | a0002c0024t0001g0086 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-38+26957G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352638 | ||||||
| chr8:27352872
|
A | G | 4 | a0001c0001t0003g0036a0002c0006t0001g0286a0002c0006t0001g0287others(1): Show | 4 | HG02615.hp2 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+27191A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352872 | ||||||
| chr8:27353000
|
G | A | 1 | a0001c0001t0003g0276 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-38+27319G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353000 | ||||||
| chr8:27353001
|
G | T | 200 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(197): Show | 203 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-38+27320G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353001 | ||||||
| chr8:27353127
|
G | A | 6 | a0001c0001t0003g0294a0001c0007t0003g0303a0001c0013t0003g0301others(3): Show | 6 | HG00639.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+27446G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353127 | ||||||
| chr8:27353172
|
G | A | 2 | a0001c0001t0003g0322a0001c0002t0001g0235 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-38+27491G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353172 | ||||||
| chr8:27353293
|
A | G | 2 | a0002c0003t0002g0254a0002c0003t0002g0255 | 2 | NA18960.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-38+27612A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353293 | ||||||
| chr8:27353335
|
T | C | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+27654T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353335 | ||||||
| chr8:27353476
|
T | A | 8 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+27795T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353476 | ||||||
| chr8:27353491
|
A | C | 4 | a0001c0009t0002g0237a0002c0003t0002g0270a0002c0003t0002g0274others(1): Show | 4 | HG00423.hp1 HG02074.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+27810A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353491 | ||||||
| chr8:27353500
|
T | C | 4 | a0001c0009t0002g0237a0002c0003t0002g0270a0002c0003t0002g0274others(1): Show | 4 | HG00423.hp1 HG02074.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+27819T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353500 | ||||||
| chr8:27353551
|
T | G | 2 | a0001c0010t0003g0289a0002c0006t0001g0006 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+27870T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353551 | ||||||
| chr8:27353560
|
A | AAC | 76 | a0001c0001t0003g0054a0001c0001t0003g0088a0001c0001t0003g0273others(73): Show | 78 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-38+27891_-38+2789 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27353560 | |||||
| chr8:27353632
|
C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+27951C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353632 | ||||||
| chr8:27353640
|
G | A | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+27959G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353640 | ||||||
| chr8:27353667
|
T | C | 26 | a0001c0001t0003g0021a0001c0001t0003g0035a0001c0001t0003g0037others(23): Show | 26 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.-38+27986T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353667 | ||||||
| chr8:27353671
|
C | A | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+27990C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353671 | ||||||
| chr8:27353816
|
C | A | 218 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(215): Show | 223 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.-38+28135C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353816 | ||||||
| chr8:27353829
|
C | T | 2 | a0001c0008t0003g0114a0002c0006t0001g0010 | 2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+28148C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353829 | ||||||
| chr8:27353838
|
G | T | 3 | a0001c0008t0003g0114a0002c0006t0001g0010a0002c0006t0002g0317 | 3 | HG00738.hp1 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+28157G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353838 | ||||||
| chr8:27353859
|
A | G | 13 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0288others(10): Show | 13 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-38+28178A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353859 | ||||||
| chr8:27353908
|
G | T | 1 | a0001c0002t0001g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-38+28227G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353908 | ||||||
| chr8:27354042
|
T | G | 30 | a0001c0001t0003g0022a0001c0001t0003g0113a0001c0001t0003g0115others(27): Show | 32 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-38+28361T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354042 | ||||||
| chr8:27354198
|
C | T | 2 | a0002c0003t0002g0249a0002c0017t0002g0252 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-38+28517C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354198 | ||||||
| chr8:27354358
|
G | A | 1 | a0002c0004t0002g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-38+28677G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354358 | ||||||
| chr8:27354393
|
G | A | 110 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(107): Show | 111 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-38+28712G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354393 | ||||||
| chr8:27354423
|
A | T | 2 | a0001c0009t0002g0018a0001c0009t0002g0087 | 2 | HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-38+28742A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354423 | ||||||
| chr8:27354548
|
G | A | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+28867G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354548 | ||||||
| chr8:27354631
|
C | T | 3 | a0001c0001t0003g0093a0002c0006t0001g0020a0002c0006t0001g0323 | 3 | HG02622.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-38+28950C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354631 | ||||||
| chr8:27354716
|
C | T | 1 | a0001c0001t0003g0027 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-38+29035C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354716 | ||||||
| chr8:27354759
|
A | C | 104 | a0001c0001t0003g0022a0001c0001t0003g0054a0001c0001t0003g0113others(101): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-38+29078A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354759 | ||||||
| chr8:27354833
|
C | G | 1 | a0002c0004t0002g0225 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-38+29152C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354833 | ||||||
| chr8:27354881
|
C | T | 18 | a0001c0001t0003g0022a0001c0001t0003g0113a0001c0001t0003g0115others(15): Show | 18 | HG00639.hp1 HG00733.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-38+29200C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354881 | ||||||
| chr8:27355324
|
GGAAGAGA others(4): Show |
G | 1 | a0001c0007t0003g0279 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-38+29653_-38+2966 others(15): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27355324 | |||||
| chr8:27355637
|
G | A | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+29956G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27355637 | ||||||
| chr8:27355671
|
C | G | 1 | a0001c0001t0003g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-38+29990C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27355671 | ||||||
| chr8:27355955
|
A | C | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+30274A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27355955 | ||||||
| chr8:27355994
|
G | A | 1 | a0002c0003t0002g0275 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-38+30313G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27355994 | ||||||
| chr8:27356001
|
C | A | 74 | a0001c0001t0003g0054a0001c0001t0003g0273a0001c0001t0003g0322others(71): Show | 76 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.-38+30320C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356001 | ||||||
| chr8:27356020
|
C | CA | 8 | a0001c0001t0003g0022a0001c0001t0003g0090a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+30354dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27356020 | |||||
| chr8:27356122
|
C | T | 215 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(212): Show | 220 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.-38+30441C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356122 | ||||||
| chr8:27356204
|
G | A | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+30523G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356204 | ||||||
| chr8:27356287
|
C | T | 74 | a0001c0001t0003g0054a0001c0001t0003g0273a0001c0001t0003g0322others(71): Show | 76 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.-38+30606C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356287 | ||||||
| chr8:27356461
|
C | G | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+30780C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356461 | ||||||
| chr8:27356476
|
A | G | 1 | a0001c0007t0003g0303 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-38+30795A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356476 | ||||||
| chr8:27356559
|
T | C | 3 | a0002c0003t0002g0180a0002c0003t0002g0267a0002c0003t0002g0269 | 3 | HG02559.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-38+30878T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356559 | ||||||
| chr8:27356653
|
G | A | 2 | a0001c0001t0003g0113a0001c0001t0003g0115 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+30972G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356653 | ||||||
| chr8:27356663
|
A | G | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+30982A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356663 | ||||||
| chr8:27356827
|
A | G | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | NA18956.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-38+31146A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356827 | ||||||
| chr8:27356865
|
T | G | 3 | a0002c0006t0001g0234a0002c0006t0001g0290a0002c0006t0001g0291 | 3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-38+31184T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356865 | ||||||
| chr8:27356929
|
G | A | 1 | a0002c0003t0002g0207 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-38+31248G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356929 | ||||||
| chr8:27357071
|
G | C | 1 | a0002c0003t0002g0254 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-38+31390G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27357071 | ||||||
| chr8:27357092
|
G | C | 1 | a0001c0007t0003g0137 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-38+31411G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27357092 | ||||||
| chr8:27357379
|
A | C | 1 | a0001c0009t0002g0313 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-38+31698A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27357379 | ||||||
| chr8:27357575
|
G | T | 4 | a0001c0001t0003g0276a0001c0007t0003g0279a0001c0007t0003g0280others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+31894G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27357575 | ||||||
| chr8:27357994
|
C | A | 7 | a0001c0001t0003g0021a0001c0001t0003g0037a0001c0001t0003g0040others(4): Show | 7 | HG00438.hp1 HG02135.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+32313C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27357994 | ||||||
| chr8:27358040
|
G | A | 28 | a0001c0001t0003g0022a0001c0001t0003g0113a0001c0001t0003g0115others(25): Show | 30 | HG00639.hp1 HG00733.hp1 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.-38+32359G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27358040 | ||||||
| chr8:27358085
|
A | G | 1 | a0002c0003t0002g0251 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-38+32404A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27358085 | ||||||
| chr8:27358208
|
C | T | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+32527C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27358208 | ||||||
| chr8:27358294
|
T | C | 4 | a0001c0001t0003g0113a0001c0001t0003g0115a0001c0021t0004g0009others(1): Show | 4 | HG02818.hp2 HG02922.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+32613T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27358294 | ||||||
| chr8:27358376
|
A | G | 1 | a0001c0001t0003g0097 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-38+32695A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27358376 | ||||||
| chr8:27359020
|
T | C | 9 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38+33339T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359020 | ||||||
| chr8:27359165
|
G | C | 1 | a0002c0006t0001g0287 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-38+33484G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359165 | ||||||
| chr8:27359178
|
C | T | 10 | a0001c0001t0003g0093a0001c0001t0003g0113a0001c0001t0003g0115others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38+33497C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359178 | ||||||
| chr8:27359275
|
T | A | 1 | a0001c0001t0003g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-38+33594T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359275 | ||||||
| chr8:27359367
|
C | T | 1 | a0001c0002t0001g0170 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-38+33686C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359367 | ||||||
| chr8:27359371
|
C | T | 1 | a0001c0001t0003g0051 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-38+33690C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359371 | ||||||
| chr8:27359396
|
G | A | 1 | a0001c0001t0003g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-38+33715G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359396 | ||||||
| chr8:27359422
|
A | T | 1 | a0002c0004t0002g0011 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-38+33741A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359422 | ||||||
| chr8:27359443
|
G | C | 4 | a0001c0009t0002g0237a0002c0003t0002g0270a0002c0003t0002g0274others(1): Show | 4 | HG00423.hp1 HG02074.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+33762G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359443 | ||||||
| chr8:27359496
|
G | T | 7 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(4): Show | 7 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+33815G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359496 | ||||||
| chr8:27359501
|
T | C | 1 | a0002c0005t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-38+33820T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359501 | ||||||
| chr8:27359531
|
A | T | 1 | a0002c0004t0002g0011 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-38+33850A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359531 | ||||||
| chr8:27359942
|
A | AACATCCT others(3): Show |
1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+34263_-38+3427 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27359942 | |||||
| chr8:27359945
|
A | G | 1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-38+34264A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359945 | ||||||
| chr8:27360246
|
C | T | 70 | a0001c0001t0003g0054a0001c0001t0003g0273a0001c0001t0003g0322others(67): Show | 72 | HG00099.hp2 HG00408.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.-38+34565C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360246 | ||||||
| chr8:27360392
|
C | T | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-38+34711C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360392 | ||||||
| chr8:27360574
|
G | A | 1 | a0002c0006t0001g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-38+34893G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360574 | ||||||
| chr8:27360612
|
G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-38+34931G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360612 | ||||||
| chr8:27360663
|
T | C | 1 | a0002c0006t0001g0068 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-38+34982T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360663 | ||||||
| chr8:27360716
|
T | G | 1 | a0001c0001t0003g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-38+35035T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360716 | ||||||
| chr8:27360815
|
C | T | 9 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38+35134C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360815 | ||||||
| chr8:27360859
|
A | G | 212 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(209): Show | 217 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-38+35178A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360859 | ||||||
| chr8:27360875
|
A | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35194A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360875 | ||||||
| chr8:27360882
|
C | G | 1 | a0001c0002t0001g0077 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-38+35201C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360882 | ||||||
| chr8:27360948
|
A | C | 19 | a0001c0001t0003g0022a0001c0001t0003g0113a0001c0001t0003g0115others(16): Show | 19 | HG00639.hp1 HG00733.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-38+35267A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360948 | ||||||
| chr8:27360975
|
G | C | 2 | a0001c0001t0003g0113a0001c0001t0003g0115 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+35294G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360975 | ||||||
| chr8:27360993
|
A | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35312A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360993 | ||||||
| chr8:27360994
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35313C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360994 | ||||||
| chr8:27361047
|
G | A | 2 | a0002c0003t0002g0249a0002c0017t0002g0252 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-38+35366G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361047 | ||||||
| chr8:27361060
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35379C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361060 | ||||||
| chr8:27361074
|
C | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35393C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361074 | ||||||
| chr8:27361075
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35394T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361075 | ||||||
| chr8:27361115
|
C | G | 1 | a0001c0001t0003g0051 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-38+35434C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361115 | ||||||
| chr8:27361119
|
C | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35438C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361119 | ||||||
| chr8:27361134
|
C | T | 1 | a0001c0002t0001g0152 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-38+35453C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361134 | ||||||
| chr8:27361139
|
A | G | 2 | a0001c0001t0003g0113a0001c0001t0003g0115 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+35458A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361139 | ||||||
| chr8:27361220
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35539T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361220 | ||||||
| chr8:27361231
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35550T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361231 | ||||||
| chr8:27361265
|
C | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35584C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361265 | ||||||
| chr8:27361283
|
A | G | 1 | a0002c0003t0002g0253 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-38+35602A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361283 | ||||||
| chr8:27361327
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35646T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361327 | ||||||
| chr8:27361329
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35648C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361329 | ||||||
| chr8:27361340
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35659T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361340 | ||||||
| chr8:27361341
|
C | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35660C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361341 | ||||||
| chr8:27361343
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35662C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361343 | ||||||
| chr8:27361351
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35670T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361351 | ||||||
| chr8:27361359
|
C | T | 2 | a0001c0009t0002g0106a0005c0016t0002g0105 | 2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.-38+35678C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361359 | ||||||
| chr8:27361373
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35692C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361373 | ||||||
| chr8:27361374
|
A | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35693A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361374 | ||||||
| chr8:27361375
|
T | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35694T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361375 | ||||||
| chr8:27361390
|
T | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35709T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361390 | ||||||
| chr8:27361395
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35714T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361395 | ||||||
| chr8:27361398
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35717C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361398 | ||||||
| chr8:27361399
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35718T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361399 | ||||||
| chr8:27361401
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35720T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361401 | ||||||
| chr8:27361424
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35743T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361424 | ||||||
| chr8:27361442
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35761T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361442 | ||||||
| chr8:27361450
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35769C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361450 | ||||||
| chr8:27361451
|
T | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35770T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361451 | ||||||
| chr8:27361453
|
G | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35772G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361453 | ||||||
| chr8:27361455
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35774C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361455 | ||||||
| chr8:27361463
|
A | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35782A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361463 | ||||||
| chr8:27361464
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35783T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361464 | ||||||
| chr8:27361480
|
T | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35799T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361480 | ||||||
| chr8:27361482
|
C | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35801C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361482 | ||||||
| chr8:27361489
|
G | T | 1 | a0001c0002t0001g0172 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-38+35808G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361489 | ||||||
| chr8:27361491
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35810T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361491 | ||||||
| chr8:27361512
|
C | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35831C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361512 | ||||||
| chr8:27361513
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35832C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361513 | ||||||
| chr8:27361515
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35834C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361515 | ||||||
| chr8:27361518
|
C | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35837C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361518 | ||||||
| chr8:27361521
|
G | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35840G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361521 | ||||||
| chr8:27361530
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35849T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361530 | ||||||
| chr8:27361537
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35856T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361537 | ||||||
| chr8:27361538
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35857T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361538 | ||||||
| chr8:27361539
|
A | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35858A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361539 | ||||||
| chr8:27361546
|
A | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35865A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361546 | ||||||
| chr8:27361548
|
A | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35867A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361548 | ||||||
| chr8:27361549
|
G | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35868G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361549 | ||||||
| chr8:27361550
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35869C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361550 | ||||||
| chr8:27361554
|
C | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35873C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361554 | ||||||
| chr8:27361555
|
C | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35874C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361555 | ||||||
| chr8:27361559
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35878G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361559 | ||||||
| chr8:27361560
|
A | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35879A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361560 | ||||||
| chr8:27361561
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35880C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361561 | ||||||
| chr8:27361563
|
G | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35882G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361563 | ||||||
| chr8:27361564
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35883G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361564 | ||||||
| chr8:27361566
|
C | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35885C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361566 | ||||||
| chr8:27361571
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35890T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361571 | ||||||
| chr8:27361571
|
T | G | 1 | a0002c0004t0002g0011 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-38+35890T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361571 | ||||||
| chr8:27361572
|
G | T | 2 | a0001c0001t0003g0048a0002c0004t0002g0011 | 2 | NA18956.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-38+35891G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361572 | ||||||
| chr8:27361573
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35892G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361573 | ||||||
| chr8:27361601
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35920T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361601 | ||||||
| chr8:27361611
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35930G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361611 | ||||||
| chr8:27361614
|
C | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35933C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361614 | ||||||
| chr8:27361615
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35933T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361615 | ||||||
| chr8:27361620
|
T | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35928T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361620 | ||||||
| chr8:27361621
|
A | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35927A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361621 | ||||||
| chr8:27361622
|
G | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35926G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361622 | ||||||
| chr8:27361623
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35925G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361623 | ||||||
| chr8:27361629
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35919T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361629 | ||||||
| chr8:27361632
|
G | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35916G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361632 | ||||||
| chr8:27361639
|
A | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35909A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361639 | ||||||
| chr8:27361640
|
G | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35908G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361640 | ||||||
| chr8:27361646
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35902T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361646 | ||||||
| chr8:27361654
|
A | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35894A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361654 | ||||||
| chr8:27361667
|
A | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35881A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361667 | ||||||
| chr8:27361675
|
A | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35873A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361675 | ||||||
| chr8:27361685
|
C | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35863C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361685 | ||||||
| chr8:27361688
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35860T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361688 | ||||||
| chr8:27361702
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35846T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361702 | ||||||
| chr8:27361711
|
G | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35837G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361711 | ||||||
| chr8:27361713
|
C | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35835C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361713 | ||||||
| chr8:27361715
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35833C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361715 | ||||||
| chr8:27361717
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35831C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361717 | ||||||
| chr8:27361732
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35816G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361732 | ||||||
| chr8:27361752
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35796G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361752 | ||||||
| chr8:27361758
|
C | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35790C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361758 | ||||||
| chr8:27361759
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35789T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361759 | ||||||
| chr8:27361760
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35788G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361760 | ||||||
| chr8:27361808
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35740C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361808 | ||||||
| chr8:27361828
|
G | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35720G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361828 | ||||||
| chr8:27361829
|
C | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35719C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361829 | ||||||
| chr8:27361841
|
G | A | 1 | a0002c0026t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-37-35707G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361841 | ||||||
| chr8:27361851
|
C | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35697C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361851 | ||||||
| chr8:27361858
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35690T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361858 | ||||||
| chr8:27361859
|
G | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35689G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361859 | ||||||
| chr8:27361864
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35684T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361864 | ||||||
| chr8:27361880
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35668T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361880 | ||||||
| chr8:27361909
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35639T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361909 | ||||||
| chr8:27361910
|
C | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35638C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361910 | ||||||
| chr8:27361911
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35637T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361911 | ||||||
| chr8:27361913
|
A | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35635A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361913 | ||||||
| chr8:27361918
|
C | T | 19 | a0001c0009t0002g0103a0001c0009t0002g0106a0001c0012t0004g0211others(16): Show | 19 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-35630C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361918 | ||||||
| chr8:27361928
|
A | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35620A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361928 | ||||||
| chr8:27361956
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35592G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361956 | ||||||
| chr8:27361980
|
A | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35568A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361980 | ||||||
| chr8:27361981
|
G | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35567G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361981 | ||||||
| chr8:27361991
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35557C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361991 | ||||||
| chr8:27361995
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35553C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361995 | ||||||
| chr8:27362000
|
C | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35548C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362000 | ||||||
| chr8:27362013
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35535T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362013 | ||||||
| chr8:27362024
|
C | CACTGTCC others(6): Show |
1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35524_-37-3552 others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362024 | ||||||
| chr8:27362032
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35516G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362032 | ||||||
| chr8:27362033
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35515T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362033 | ||||||
| chr8:27362035
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35513T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362035 | ||||||
| chr8:27362045
|
A | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35503A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362045 | ||||||
| chr8:27362059
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35489T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362059 | ||||||
| chr8:27362060
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35488T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362060 | ||||||
| chr8:27362074
|
C | T | 15 | a0001c0009t0002g0103a0001c0012t0004g0211a0002c0004t0002g0094others(12): Show | 15 | HG00438.hp2 HG00741.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-37-35474C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362074 | ||||||
| chr8:27362076
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35472T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362076 | ||||||
| chr8:27362083
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35465G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362083 | ||||||
| chr8:27362093
|
G | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35455G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362093 | ||||||
| chr8:27362100
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35448T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362100 | ||||||
| chr8:27362200
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35348T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362200 | ||||||
| chr8:27362201
|
A | G | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35347A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362201 | ||||||
| chr8:27362202
|
G | T | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35346G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362202 | ||||||
| chr8:27362211
|
G | T | 1 | a0001c0001t0003g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-37-35337G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362211 | ||||||
| chr8:27362212
|
GCAGCACC others(6): Show |
G | 1 | a0001c0001t0003g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-37-35334_-37-3532 others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27362212 | |||||
| chr8:27362219
|
C | T | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-35329C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362219 | ||||||
| chr8:27362227
|
T | C | 1 | a0001c0001t0003g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-37-35321T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362227 | ||||||
| chr8:27362234
|
T | A | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35314T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362234 | ||||||
| chr8:27362337
|
C | A | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-35211C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362337 | ||||||
| chr8:27362470
|
C | T | 84 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(81): Show | 85 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-37-35078C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362470 | ||||||
| chr8:27362771
|
C | T | 2 | a0001c0008t0003g0114a0002c0006t0001g0010 | 2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-37-34777C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362771 | ||||||
| chr8:27362793
|
G | A | 112 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(109): Show | 113 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.-37-34755G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362793 | ||||||
| chr8:27362808
|
TCTCCCAC others(16): Show |
T | 2 | a0002c0004t0002g0109a0002c0004t0002g0110 | 2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-37-34710_-37-3468 others(27): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27362808 | |||||
| chr8:27363116
|
GA | G | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-34431delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363116 | ||||||
| chr8:27363249
|
C | T | 9 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-34299C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363249 | ||||||
| chr8:27363254
|
C | T | 9 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-34294C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363254 | ||||||
| chr8:27363291
|
G | A | 3 | a0002c0003t0002g0239a0002c0003t0002g0240a0002c0003t0002g0241 | 3 | HG00408.hp2 NA18947.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-37-34257G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363291 | ||||||
| chr8:27363311
|
G | A | 7 | a0001c0012t0004g0053a0001c0012t0004g0057a0002c0003t0002g0023others(4): Show | 7 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-34237G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363311 | ||||||
| chr8:27363323
|
A | C | 1 | a0001c0001t0003g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-34225A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363323 | ||||||
| chr8:27363323
|
A | G | 6 | a0001c0001t0003g0021a0001c0001t0003g0037a0001c0001t0003g0040others(3): Show | 6 | HG00438.hp1 HG02135.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-34225A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363323 | ||||||
| chr8:27363592
|
G | A | 9 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-33956G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363592 | ||||||
| chr8:27363665
|
T | A | 1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-37-33883T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363665 | ||||||
| chr8:27363701
|
T | C | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-33847T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363701 | ||||||
| chr8:27363944
|
G | C | 3 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115 | 3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-33604G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363944 | ||||||
| chr8:27364133
|
A | G | 3 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295 | 3 | HG02109.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-37-33415A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364133 | ||||||
| chr8:27364166
|
T | C | 2 | a0001c0002t0001g0147a0001c0002t0001g0166 | 2 | HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-37-33382T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364166 | ||||||
| chr8:27364375
|
C | T | 2 | a0002c0004t0002g0109a0002c0004t0002g0110 | 2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-37-33173C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364375 | ||||||
| chr8:27364470
|
G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-37-33078G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364470 | ||||||
| chr8:27364470
|
G | C | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-33078G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364470 | ||||||
| chr8:27364489
|
C | T | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-33059C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364489 | ||||||
| chr8:27364563
|
A | T | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-32985A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364563 | ||||||
| chr8:27364670
|
G | A | 2 | a0001c0001t0003g0059a0001c0001t0005g0060 | 2 | HG01069.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-37-32878G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364670 | ||||||
| chr8:27364945
|
A | G | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-37-32603A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364945 | ||||||
| chr8:27364962
|
C | T | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-32586C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364962 | ||||||
| chr8:27365026
|
C | A | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-37-32522C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365026 | ||||||
| chr8:27365188
|
G | A | 2 | a0001c0010t0003g0289a0002c0006t0001g0006 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-37-32360G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365188 | ||||||
| chr8:27365298
|
G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-37-32250G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365298 | ||||||
| chr8:27365370
|
T | C | 3 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295 | 3 | HG02109.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-37-32178T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365370 | ||||||
| chr8:27365448
|
C | T | 1 | a0001c0002t0001g0176 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-37-32100C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365448 | ||||||
| chr8:27365637
|
G | T | 2 | a0001c0001t0003g0322a0001c0002t0001g0235 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-37-31911G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365637 | ||||||
| chr8:27365655
|
C | CTTT | 31 | a0001c0001t0003g0022a0001c0001t0003g0088a0001c0001t0003g0113others(28): Show | 33 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-37-31893_-37-3189 others(7): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365655 | ||||||
| chr8:27365811
|
G | A | 2 | a0001c0010t0003g0289a0002c0006t0001g0006 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-37-31737G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365811 | ||||||
| chr8:27365825
|
T | C | 76 | a0001c0001t0003g0054a0001c0001t0003g0273a0001c0001t0003g0322others(73): Show | 78 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-37-31723T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365825 | ||||||
| chr8:27365840
|
C | T | 2 | a0001c0010t0003g0285a0010c0032t0003g0284 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-37-31708C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365840 | ||||||
| chr8:27365900
|
A | G | 2 | a0001c0001t0003g0036a0001c0013t0003g0304 | 2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-37-31648A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365900 | ||||||
| chr8:27365957
|
T | C | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-31591T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365957 | ||||||
| chr8:27366121
|
G | A | 2 | a0001c0010t0003g0289a0002c0006t0001g0006 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-37-31427G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366121 | ||||||
| chr8:27366165
|
G | A | 76 | a0001c0001t0003g0054a0001c0001t0003g0273a0001c0001t0003g0322others(73): Show | 78 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-37-31383G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366165 | ||||||
| chr8:27366279
|
A | G | 19 | a0001c0009t0002g0103a0001c0009t0002g0106a0001c0012t0004g0211others(16): Show | 19 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-31269A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366279 | ||||||
| chr8:27366339
|
A | G | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-31209A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366339 | ||||||
| chr8:27366579
|
T | C | 1 | a0002c0026t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-37-30969T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366579 | ||||||
| chr8:27366803
|
TG | T | 3 | a0002c0003t0002g0247a0002c0004t0002g0224a0002c0004t0002g0225 | 3 | HG01261.hp1 HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-37-30743delG | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27366803 | |||||
| chr8:27366816
|
A | G | 9 | a0001c0002t0001g0312a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-30732A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366816 | ||||||
| chr8:27366880
|
G | A | 1 | a0001c0025t0001g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-37-30668G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366880 | ||||||
| chr8:27366909
|
C | T | 1 | a0002c0003t0002g0255 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-37-30639C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366909 | ||||||
| chr8:27366993
|
G | A | 18 | a0001c0001t0003g0022a0001c0001t0003g0088a0001c0001t0003g0113others(15): Show | 18 | HG00639.hp1 HG00733.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-37-30555G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366993 | ||||||
| chr8:27367229
|
C | T | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-30319C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367229 | ||||||
| chr8:27367280
|
T | C | 31 | a0001c0001t0003g0022a0001c0001t0003g0088a0001c0001t0003g0113others(28): Show | 33 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-37-30268T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367280 | ||||||
| chr8:27367290
|
A | G | 1 | a0001c0001t0003g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-37-30258A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367290 | ||||||
| chr8:27367390
|
G | A | 1 | a0001c0001t0003g0071 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-37-30158G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367390 | ||||||
| chr8:27367409
|
C | T | 2 | a0001c0007t0003g0280a0001c0007t0003g0281 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-37-30139C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367409 | ||||||
| chr8:27367439
|
G | A | 1 | a0002c0003t0002g0271 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-37-30109G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367439 | ||||||
| chr8:27367503
|
C | G | 2 | a0001c0010t0003g0289a0002c0006t0001g0006 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-37-30045C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367503 | ||||||
| chr8:27367799
|
A | G | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-29749A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367799 | ||||||
| chr8:27367801
|
A | G | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-29747A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367801 | ||||||
| chr8:27368125
|
C | T | 4 | a0001c0001t0003g0276a0001c0007t0003g0279a0001c0007t0003g0280others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-29423C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368125 | ||||||
| chr8:27368126
|
G | A | 1 | a0001c0025t0001g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-37-29422G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368126 | ||||||
| chr8:27368278
|
G | A | 1 | a0001c0001t0003g0318 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-37-29270G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368278 | ||||||
| chr8:27368452
|
C | T | 1 | a0002c0003t0002g0266 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-37-29096C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368452 | ||||||
| chr8:27368513
|
C | G | 3 | a0001c0001t0003g0050a0002c0005t0001g0194a0002c0005t0001g0195 | 3 | HG01256.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-37-29035C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368513 | ||||||
| chr8:27368669
|
A | T | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-28879A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368669 | ||||||
| chr8:27368824
|
G | C | 7 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-28724G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368824 | ||||||
| chr8:27368895
|
G | T | 3 | a0001c0002t0001g0119a0001c0002t0001g0121a0001c0002t0001g0122 | 3 | NA18957.hp2 NA18969.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-37-28653G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368895 | ||||||
| chr8:27368915
|
G | C | 7 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-28633G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368915 | ||||||
| chr8:27368919
|
G | A | 1 | a0001c0002t0001g0170 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-37-28629G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368919 | ||||||
| chr8:27369219
|
C | G | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-28329C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369219 | ||||||
| chr8:27369239
|
T | C | 8 | a0001c0009t0002g0310a0001c0009t0002g0313a0002c0003t0002g0012others(5): Show | 10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-28309T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369239 | ||||||
| chr8:27369241
|
C | T | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-28307C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369241 | ||||||
| chr8:27369273
|
A | C | 124 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(121): Show | 125 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-37-28275A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369273 | ||||||
| chr8:27369401
|
G | A | 1 | a0001c0001t0003g0322 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-37-28147G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369401 | ||||||
| chr8:27369533
|
G | A | 1 | a0002c0004t0002g0248 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-37-28015G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369533 | ||||||
| chr8:27369536
|
G | C | 3 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295 | 3 | HG02109.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-37-28012G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369536 | ||||||
| chr8:27369609
|
G | A | 6 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(3): Show | 6 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-27939G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369609 | ||||||
| chr8:27369714
|
C | G | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-37-27834C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369714 | ||||||
| chr8:27369819
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-37-27729A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369819 | ||||||
| chr8:27369887
|
G | C | 3 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115 | 3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-27661G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369887 | ||||||
| chr8:27369909
|
G | A | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-27639G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369909 | ||||||
| chr8:27369925
|
T | C | 28 | a0001c0001t0003g0022a0001c0001t0003g0088a0001c0001t0003g0113others(25): Show | 30 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-37-27623T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369925 | ||||||
| chr8:27369934
|
A | G | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-37-27614A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369934 | ||||||
| chr8:27369936
|
C | T | 109 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(106): Show | 110 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-37-27612C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369936 | ||||||
| chr8:27370037
|
A | G | 82 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(79): Show | 83 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-37-27511A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370037 | ||||||
| chr8:27370117
|
C | T | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-27431C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370117 | ||||||
| chr8:27370169
|
G | T | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-27379G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370169 | ||||||
| chr8:27370321
|
C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-27227C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370321 | ||||||
| chr8:27370322
|
G | A | 1 | a0002c0004t0002g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-37-27226G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370322 | ||||||
| chr8:27370496
|
C | T | 1 | a0001c0010t0003g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-37-27052C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370496 | ||||||
| chr8:27370545
|
A | C | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-27003A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370545 | ||||||
| chr8:27370559
|
G | A | 13 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(10): Show | 13 | HG00639.hp1 HG00733.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-37-26989G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370559 | ||||||
| chr8:27370567
|
T | G | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-26981T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370567 | ||||||
| chr8:27370600
|
G | T | 1 | a0001c0001t0003g0071 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-37-26948G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370600 | ||||||
| chr8:27370677
|
T | C | 2 | a0001c0002t0001g0192a0002c0005t0001g0202 | 2 | HG00408.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-37-26871T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370677 | ||||||
| chr8:27370839
|
C | G | 8 | a0001c0009t0002g0310a0001c0009t0002g0313a0002c0003t0002g0012others(5): Show | 10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-26709C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370839 | ||||||
| chr8:27370897
|
C | G | 4 | a0001c0001t0003g0024a0002c0005t0001g0026a0002c0005t0001g0031others(1): Show | 4 | HG01928.hp1 HG01943.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-26651C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370897 | ||||||
| chr8:27370986
|
C | T | 5 | a0001c0001t0003g0050a0002c0005t0001g0194a0002c0005t0001g0195others(2): Show | 5 | HG01081.hp2 HG01123.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-26562C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370986 | ||||||
| chr8:27371045
|
G | A | 8 | a0001c0009t0002g0310a0001c0009t0002g0313a0002c0003t0002g0012others(5): Show | 10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-26503G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371045 | ||||||
| chr8:27371061
|
A | G | 1 | a0001c0012t0004g0211 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-37-26487A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371061 | ||||||
| chr8:27371110
|
G | C | 1 | a0001c0002t0001g0192 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-37-26438G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371110 | ||||||
| chr8:27371149
|
C | A | 112 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(109): Show | 113 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.-37-26399C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371149 | ||||||
| chr8:27371158
|
C | T | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-26390C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371158 | ||||||
| chr8:27371185
|
C | T | 1 | a0002c0004t0002g0110 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-37-26363C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371185 | ||||||
| chr8:27371292
|
G | A | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-37-26256G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371292 | ||||||
| chr8:27371325
|
G | A | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-26223G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371325 | ||||||
| chr8:27371338
|
G | A | 1 | a0002c0003t0002g0266 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-37-26210G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371338 | ||||||
| chr8:27371443
|
C | T | 1 | a0002c0018t0002g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-37-26105C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371443 | ||||||
| chr8:27371545
|
T | TTA | 18 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0276others(15): Show | 18 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-37-25987_-37-2598 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27371545 | |||||
| chr8:27371545
|
T | TTATA | 109 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(106): Show | 110 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-37-25989_-37-2598 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27371545 | |||||
| chr8:27371793
|
C | T | 3 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115 | 3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-25755C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371793 | ||||||
| chr8:27371905
|
C | T | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-25643C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371905 | ||||||
| chr8:27371910
|
C | T | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-37-25638C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371910 | ||||||
| chr8:27371927
|
G | A | 4 | a0001c0002t0001g0080a0001c0002t0001g0170a0001c0002t0001g0171others(1): Show | 4 | NA18945.hp1 NA18967.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-25621G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371927 | ||||||
| chr8:27371944
|
A | G | 1 | a0002c0006t0001g0068 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-37-25604A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371944 | ||||||
| chr8:27371987
|
CAT | C | 3 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295 | 3 | HG02109.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-37-25558_-37-2555 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27371987 | |||||
| chr8:27372004
|
G | A | 2 | a0002c0003t0002g0307a0002c0003t0002g0308 | 2 | NA18967.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-37-25544G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372004 | ||||||
| chr8:27372040
|
T | C | 2 | a0001c0011t0001g0142a0001c0011t0001g0165 | 2 | NA18949.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-37-25508T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372040 | ||||||
| chr8:27372076
|
G | A | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-25472G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372076 | ||||||
| chr8:27372109
|
T | C | 1 | a0002c0026t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-37-25439T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372109 | ||||||
| chr8:27372126
|
A | G | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-25422A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372126 | ||||||
| chr8:27372199
|
G | A | 8 | a0001c0009t0002g0310a0001c0009t0002g0313a0002c0003t0002g0012others(5): Show | 10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-25349G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372199 | ||||||
| chr8:27372220
|
G | T | 1 | a0001c0002t0001g0162 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-37-25328G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372220 | ||||||
| chr8:27372520
|
G | A | 11 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(8): Show | 11 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-25028G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372520 | ||||||
| chr8:27372947
|
G | A | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-24601G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372947 | ||||||
| chr8:27372948
|
C | T | 2 | a0001c0008t0003g0114a0002c0006t0001g0010 | 2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-37-24600C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372948 | ||||||
| chr8:27372955
|
A | T | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-37-24593A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372955 | ||||||
| chr8:27372961
|
T | C | 2 | a0002c0003t0002g0004a0002c0003t0002g0264 | 3 | HG01257.hp2 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-37-24587T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372961 | ||||||
| chr8:27373058
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-37-24490A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373058 | ||||||
| chr8:27373061
|
T | C | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-24487T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373061 | ||||||
| chr8:27373120
|
A | G | 122 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(119): Show | 123 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-37-24428A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373120 | ||||||
| chr8:27373159
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-37-24389G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373159 | ||||||
| chr8:27373301
|
C | T | 8 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-24247C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373301 | ||||||
| chr8:27373302
|
A | G | 148 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(145): Show | 151 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-37-24246A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373302 | ||||||
| chr8:27373408
|
T | G | 223 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(220): Show | 228 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-37-24140T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373408 | ||||||
| chr8:27373698
|
T | A | 17 | a0001c0001t0003g0022a0001c0001t0003g0046a0001c0001t0003g0088others(14): Show | 17 | HG00733.hp1 HG00738.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-37-23850T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373698 | ||||||
| chr8:27373699
|
A | T | 9 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0175others(6): Show | 9 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37-23849A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373699 | ||||||
| chr8:27373803
|
A | G | 1 | a0002c0003t0006g0044 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-37-23745A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373803 | ||||||
| chr8:27373890
|
G | T | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-23658G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373890 | ||||||
| chr8:27373976
|
G | A | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-23572G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373976 | ||||||
| chr8:27374040
|
G | A | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-23508G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374040 | ||||||
| chr8:27374071
|
A | T | 74 | a0001c0001t0003g0054a0001c0009t0002g0018a0001c0009t0002g0087others(71): Show | 76 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.-37-23477A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374071 | ||||||
| chr8:27374092
|
G | A | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-23456G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374092 | ||||||
| chr8:27374170
|
T | G | 9 | a0001c0002t0001g0144a0001c0002t0001g0155a0001c0002t0001g0158others(6): Show | 9 | HG00544.hp2 HG02015.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37-23378T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374170 | ||||||
| chr8:27374256
|
G | A | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-23292G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374256 | ||||||
| chr8:27374304
|
CTTGGGAT others(3): Show |
C | 2 | a0001c0011t0001g0098a0001c0011t0001g0151 | 2 | NA18961.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-37-23241_-37-2323 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27374304 | |||||
| chr8:27374346
|
C | T | 8 | a0001c0009t0002g0310a0001c0009t0002g0313a0002c0003t0002g0012others(5): Show | 10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-23202C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374346 | ||||||
| chr8:27374462
|
G | A | 1 | a0002c0005t0001g0002 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-37-23086G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374462 | ||||||
| chr8:27374501
|
T | C | 142 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(139): Show | 145 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-37-23047T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374501 | ||||||
| chr8:27374547
|
C | T | 26 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(23): Show | 28 | HG00639.hp1 HG00733.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-37-23001C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374547 | ||||||
| chr8:27374548
|
G | A | 2 | a0002c0004t0002g0109a0002c0004t0002g0110 | 2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-37-23000G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374548 | ||||||
| chr8:27374673
|
C | G | 1 | a0002c0006t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-37-22875C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374673 | ||||||
| chr8:27374707
|
A | G | 1 | a0002c0004t0002g0242 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-37-22841A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374707 | ||||||
| chr8:27374777
|
G | A | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-22771G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374777 | ||||||
| chr8:27374808
|
G | A | 1 | a0002c0004t0002g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-37-22740G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374808 | ||||||
| chr8:27374894
|
ATG | A | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-22651_-37-2265 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27374894 | |||||
| chr8:27375430
|
T | C | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-22118T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375430 | ||||||
| chr8:27375492
|
C | T | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-37-22056C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375492 | ||||||
| chr8:27375569
|
A | G | 2 | a0002c0003t0002g0249a0002c0017t0002g0252 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-37-21979A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375569 | ||||||
| chr8:27375665
|
G | A | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-21883G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375665 | ||||||
| chr8:27375678
|
G | A | 2 | a0001c0009t0002g0018a0001c0009t0002g0087 | 2 | HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-37-21870G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375678 | ||||||
| chr8:27375726
|
C | T | 2 | a0002c0004t0002g0109a0002c0004t0002g0110 | 2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-37-21822C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375726 | ||||||
| chr8:27375815
|
C | T | 8 | a0001c0009t0002g0310a0001c0009t0002g0313a0002c0003t0002g0012others(5): Show | 10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-21733C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375815 | ||||||
| chr8:27376070
|
A | G | 3 | a0001c0001t0003g0095a0001c0001t0003g0096a0001c0001t0003g0097 | 3 | HG00323.hp2 HG01515.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-37-21478A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376070 | ||||||
| chr8:27376179
|
C | A | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-21369C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376179 | ||||||
| chr8:27376216
|
G | A | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-21332G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376216 | ||||||
| chr8:27376316
|
T | A | 1 | a0002c0003t0002g0207 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-37-21232T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376316 | ||||||
| chr8:27376387
|
G | C | 4 | a0001c0002t0001g0080a0001c0002t0001g0170a0001c0002t0001g0171others(1): Show | 4 | NA18945.hp1 NA18967.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-21161G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376387 | ||||||
| chr8:27376507
|
C | G | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-21041C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376507 | ||||||
| chr8:27376633
|
G | A | 2 | a0002c0004t0002g0244a0002c0004t0002g0245 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-37-20915G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376633 | ||||||
| chr8:27376661
|
G | A | 2 | a0001c0008t0003g0319a0001c0008t0003g0320 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-37-20887G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376661 | ||||||
| chr8:27376776
|
A | G | 4 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-20772A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376776 | ||||||
| chr8:27376849
|
G | A | 2 | a0001c0007t0003g0280a0001c0007t0003g0281 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-37-20699G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376849 | ||||||
| chr8:27376884
|
C | T | 1 | a0001c0002t0001g0192 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-37-20664C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376884 | ||||||
| chr8:27376930
|
C | T | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-20618C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376930 | ||||||
| chr8:27376994
|
C | A | 1 | a0001c0002t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-37-20554C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376994 | ||||||
| chr8:27377074
|
G | A | 4 | a0001c0007t0003g0135a0001c0007t0003g0136a0001c0007t0003g0137others(1): Show | 4 | HG00735.hp2 HG01993.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-20474G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377074 | ||||||
| chr8:27377103
|
C | G | 1 | a0001c0001t0003g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-37-20445C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377103 | ||||||
| chr8:27377154
|
C | T | 1 | a0002c0003t0002g0251 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-37-20394C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377154 | ||||||
| chr8:27377171
|
C | T | 6 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-20377C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377171 | ||||||
| chr8:27377215
|
G | A | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-20333G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377215 | ||||||
| chr8:27377314
|
C | A | 3 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295 | 3 | HG02109.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-37-20234C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377314 | ||||||
| chr8:27377360
|
G | A | 1 | a0001c0002t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-37-20188G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377360 | ||||||
| chr8:27377363
|
A | C | 1 | a0001c0002t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-37-20185A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377363 | ||||||
| chr8:27377416
|
G | A | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-20132G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377416 | ||||||
| chr8:27377479
|
T | C | 1 | a0001c0002t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-37-20069T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377479 | ||||||
| chr8:27377703
|
C | T | 6 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-19845C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377703 | ||||||
| chr8:27377794
|
C | G | 1 | a0002c0004t0002g0215 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-37-19754C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377794 | ||||||
| chr8:27377934
|
T | C | 1 | a0001c0002t0001g0296 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-37-19614T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377934 | ||||||
| chr8:27378011
|
C | T | 2 | a0001c0001t0003g0059a0001c0001t0005g0060 | 2 | HG01069.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-37-19537C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378011 | ||||||
| chr8:27378274
|
T | G | 1 | a0001c0001t0003g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37-19274T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378274 | ||||||
| chr8:27378301
|
G | A | 73 | a0001c0001t0003g0054a0001c0009t0002g0018a0001c0009t0002g0087others(70): Show | 75 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-37-19247G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378301 | ||||||
| chr8:27378372
|
G | T | 2 | a0001c0009t0002g0018a0001c0009t0002g0087 | 2 | HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-37-19176G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378372 | ||||||
| chr8:27378480
|
C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-19068C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378480 | ||||||
| chr8:27378601
|
C | CTG | 9 | a0001c0001t0003g0294a0001c0002t0001g0080a0001c0002t0001g0122others(6): Show | 9 | HG01433.hp2 HG01993.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37-18899_-37-1889 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | |||||
| chr8:27378601
|
C | CTGTG | 5 | a0001c0002t0001g0076a0001c0002t0001g0132a0001c0002t0001g0146others(2): Show | 5 | HG00099.hp1 HG00544.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-18901_-37-1889 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | |||||
| chr8:27378601
|
CTG | C | 29 | a0001c0001t0003g0178a0001c0002t0001g0117a0001c0002t0001g0118others(26): Show | 31 | HG00323.hp1 HG00423.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.-37-18899_-37-1889 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | |||||
| chr8:27378601
|
CTGTG | C | 60 | a0001c0001t0003g0054a0001c0002t0001g0079a0001c0002t0001g0128others(57): Show | 60 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.-37-18901_-37-1889 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | |||||
| chr8:27378601
|
CTGTGTG | C | 29 | a0001c0002t0001g0147a0001c0008t0003g0114a0001c0008t0003g0315others(26): Show | 30 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-37-18903_-37-1889 others(10): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | |||||
| chr8:27378601
|
CTGTGTGT others(1): Show |
C | 16 | a0001c0001t0003g0022a0001c0002t0001g0161a0001c0009t0002g0237others(13): Show | 16 | HG00423.hp1 HG00733.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-37-18905_-37-1889 others(12): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | |||||
| chr8:27378601
|
CTGTGTGT others(3): Show |
C | 2 | a0001c0001t0003g0045a0002c0003t0002g0259 | 2 | HG03239.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-37-18907_-37-1889 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | |||||
| chr8:27378601
|
CTGTGTGT others(5): Show |
C | 18 | a0001c0001t0003g0021a0001c0001t0003g0037a0001c0001t0003g0040others(15): Show | 19 | HG00099.hp2 HG00438.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-37-18909_-37-1889 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | |||||
| chr8:27378601
|
CTGTGTGT others(7): Show |
C | 28 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0035others(25): Show | 28 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.-37-18911_-37-1889 others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | |||||
| chr8:27378601
|
CTGTGTGT others(9): Show |
C | 53 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(50): Show | 54 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.-37-18913_-37-1889 others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | |||||
| chr8:27378601
|
CTGTGTGT others(11): Show |
C | 1 | a0001c0010t0003g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-37-18915_-37-1889 others(22): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | |||||
| chr8:27378601
|
CTGTGTGT others(13): Show |
C | 12 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0288others(9): Show | 12 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37-18917_-37-1889 others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | |||||
| chr8:27378601
|
CTGTGTGT others(19): Show |
C | 7 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0183others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-18923_-37-1889 others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | |||||
| chr8:27378602
|
T | C | 2 | a0001c0008t0003g0314a0002c0006t0001g0006 | 2 | HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-37-18946T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378602 | ||||||
| chr8:27378604
|
T | C | 6 | a0001c0009t0002g0106a0002c0003t0002g0249a0002c0004t0002g0094others(3): Show | 6 | HG00423.hp2 HG00741.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-18944T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378604 | ||||||
| chr8:27378606
|
T | C | 48 | a0001c0001t0003g0054a0001c0002t0001g0296a0001c0008t0003g0243others(45): Show | 48 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-37-18942T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378606 | ||||||
| chr8:27378608
|
T | C | 27 | a0001c0008t0003g0114a0001c0008t0003g0315a0001c0008t0003g0316others(24): Show | 28 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-37-18940T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378608 | ||||||
| chr8:27378610
|
T | C | 12 | a0001c0009t0002g0237a0001c0012t0004g0030a0002c0003t0002g0223others(9): Show | 12 | HG00423.hp1 HG01175.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-37-18938T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378610 | ||||||
| chr8:27378612
|
T | C | 1 | a0002c0003t0002g0259 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-37-18936T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378612 | ||||||
| chr8:27378614
|
T | C | 7 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(4): Show | 8 | HG00099.hp2 HG00741.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-18934T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378614 | ||||||
| chr8:27378616
|
T | C | 1 | a0002c0003t0002g0270 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-37-18932T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378616 | ||||||
| chr8:27378618
|
T | C | 1 | a0002c0003t0002g0239 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-37-18930T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378618 | ||||||
| chr8:27378702
|
G | A | 4 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-18846G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378702 | ||||||
| chr8:27378711
|
G | A | 1 | a0001c0002t0001g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-37-18837G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378711 | ||||||
| chr8:27379188
|
T | C | 1 | a0002c0004t0002g0210 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-37-18360T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379188 | ||||||
| chr8:27379380
|
C | A | 8 | a0001c0009t0002g0310a0001c0009t0002g0313a0002c0003t0002g0012others(5): Show | 10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-18168C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379380 | ||||||
| chr8:27379519
|
C | T | 3 | a0002c0006t0001g0234a0002c0006t0001g0290a0002c0006t0001g0291 | 3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-37-18029C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379519 | ||||||
| chr8:27379524
|
A | G | 315 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(312): Show | 320 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.-37-18024A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379524 | ||||||
| chr8:27379689
|
A | G | 94 | a0001c0001t0003g0054a0001c0009t0002g0018a0001c0009t0002g0087others(91): Show | 96 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-37-17859A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379689 | ||||||
| chr8:27379690
|
T | C | 245 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(242): Show | 250 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-37-17858T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379690 | ||||||
| chr8:27379691
|
G | A | 1 | a0009c0019t0002g0102 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-37-17857G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379691 | ||||||
| chr8:27379741
|
A | G | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-37-17807A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379741 | ||||||
| chr8:27380141
|
G | A | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-37-17407G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27380141 | ||||||
| chr8:27380191
|
G | A | 97 | a0001c0001t0003g0054a0001c0008t0003g0314a0001c0008t0003g0315others(94): Show | 99 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-37-17357G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27380191 | ||||||
| chr8:27380535
|
AT | A | 114 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(111): Show | 115 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-37-17003delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27380535 | |||||
| chr8:27380598
|
G | C | 94 | a0001c0001t0003g0054a0001c0009t0002g0018a0001c0009t0002g0087others(91): Show | 96 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-37-16950G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27380598 | ||||||
| chr8:27380768
|
C | T | 1 | a0002c0006t0001g0213 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-37-16780C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27380768 | ||||||
| chr8:27380771
|
A | G | 5 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(2): Show | 5 | HG02109.hp2 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-16777A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27380771 | ||||||
| chr8:27381124
|
C | A | 3 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115 | 3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-16424C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381124 | ||||||
| chr8:27381243
|
A | C | 3 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115 | 3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-16305A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381243 | ||||||
| chr8:27381253
|
C | G | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-37-16295C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381253 | ||||||
| chr8:27381309
|
A | G | 94 | a0001c0001t0003g0054a0001c0009t0002g0018a0001c0009t0002g0087others(91): Show | 96 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-37-16239A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381309 | ||||||
| chr8:27381335
|
A | G | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-37-16213A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381335 | ||||||
| chr8:27381383
|
C | T | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-16165C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381383 | ||||||
| chr8:27381384
|
T | C | 2 | a0002c0003t0002g0239a0002c0003t0002g0241 | 2 | HG00408.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-37-16164T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381384 | ||||||
| chr8:27381741
|
C | T | 114 | a0001c0001t0003g0054a0001c0002t0001g0296a0001c0008t0003g0114others(111): Show | 118 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-37-15807C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381741 | ||||||
| chr8:27381777
|
A | G | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-15771A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381777 | ||||||
| chr8:27381902
|
T | C | 1 | a0002c0003t0002g0207 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-37-15646T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381902 | ||||||
| chr8:27381930
|
T | G | 1 | a0002c0006t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-37-15618T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381930 | ||||||
| chr8:27382015
|
T | A | 1 | a0002c0006t0001g0126 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-37-15533T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382015 | ||||||
| chr8:27382105
|
G | C | 2 | a0002c0004t0002g0109a0002c0004t0002g0110 | 2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-37-15443G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382105 | ||||||
| chr8:27382412
|
T | A | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-15136T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382412 | ||||||
| chr8:27382556
|
GT | G | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-14981delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27382556 | |||||
| chr8:27382582
|
A | G | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-14966A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382582 | ||||||
| chr8:27382582
|
A | T | 1 | a0002c0006t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-37-14966A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382582 | ||||||
| chr8:27382649
|
G | A | 3 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0205 | 3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-37-14899G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382649 | ||||||
| chr8:27382728
|
T | C | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-37-14820T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382728 | ||||||
| chr8:27383022
|
T | C | 1 | a0011c0033t0001g0154 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-37-14526T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383022 | ||||||
| chr8:27383038
|
A | C | 114 | a0001c0001t0003g0054a0001c0002t0001g0296a0001c0008t0003g0114others(111): Show | 118 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-37-14510A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383038 | ||||||
| chr8:27383104
|
GTC | G | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-37-14442_-37-1444 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27383104 | |||||
| chr8:27383181
|
A | G | 106 | a0001c0001t0003g0054a0001c0008t0003g0114a0001c0009t0002g0018others(103): Show | 110 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.-37-14367A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383181 | ||||||
| chr8:27383240
|
C | A | 4 | a0001c0001t0003g0276a0001c0007t0003g0279a0001c0007t0003g0280others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-14308C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383240 | ||||||
| chr8:27383365
|
C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-14183C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383365 | ||||||
| chr8:27383373
|
G | A | 2 | a0001c0002t0001g0171a0001c0002t0001g0172 | 2 | NA18981.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-37-14175G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383373 | ||||||
| chr8:27383551
|
G | A | 3 | a0001c0001t0003g0036a0001c0002t0001g0131a0002c0006t0001g0323 | 3 | HG01433.hp2 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-37-13997G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383551 | ||||||
| chr8:27383565
|
G | A | 112 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(109): Show | 116 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-37-13983G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383565 | ||||||
| chr8:27383573
|
C | T | 1 | a0002c0006t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-37-13975C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383573 | ||||||
| chr8:27383836
|
C | T | 244 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(241): Show | 249 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.-37-13712C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383836 | ||||||
| chr8:27383852
|
A | ATTTTTTT others(6): Show |
3 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010 | 3 | HG00738.hp1 HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-37-13695_-37-1368 others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27383852 | |||||
| chr8:27383852
|
A | ATTTTTTT others(7): Show |
7 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-13683_-37-1368 others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27383852 | |||||
| chr8:27383852
|
A | ATTTTTTT others(8): Show |
6 | a0001c0012t0004g0057a0001c0021t0004g0009a0002c0003t0002g0218others(3): Show | 6 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-13683_-37-1368 others(19): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27383852 | |||||
| chr8:27383852
|
A | ATTTTTTT others(9): Show |
79 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(76): Show | 83 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.-37-13683_-37-1368 others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27383852 | |||||
| chr8:27383852
|
A | ATTTTTTT others(10): Show |
19 | a0001c0009t0002g0106a0001c0009t0002g0310a0001c0012t0004g0053others(16): Show | 19 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-13683_-37-1368 others(21): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27383852 | |||||
| chr8:27383951
|
C | T | 4 | a0002c0006t0001g0006a0002c0006t0001g0234a0002c0006t0001g0290others(1): Show | 4 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-13597C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383951 | ||||||
| chr8:27383961
|
G | A | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-13587G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383961 | ||||||
| chr8:27383993
|
C | T | 2 | a0002c0003t0002g0249a0002c0017t0002g0252 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-37-13555C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383993 | ||||||
| chr8:27384000
|
C | T | 1 | a0001c0001t0003g0072 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-37-13548C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384000 | ||||||
| chr8:27384069
|
C | T | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-13479C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384069 | ||||||
| chr8:27384177
|
T | C | 9 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-13371T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384177 | ||||||
| chr8:27384226
|
A | G | 2 | a0002c0003t0002g0249a0002c0017t0002g0252 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-37-13322A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384226 | ||||||
| chr8:27384315
|
A | C | 112 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(109): Show | 116 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-37-13233A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384315 | ||||||
| chr8:27384339
|
T | C | 9 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-13209T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384339 | ||||||
| chr8:27384388
|
AAATTTGT others(5): Show |
A | 1 | a0002c0004t0002g0141 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-37-13157_-37-1314 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27384388 | |||||
| chr8:27384589
|
A | G | 4 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(1): Show | 4 | HG02572.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-12959A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384589 | ||||||
| chr8:27384660
|
A | G | 1 | a0001c0011t0001g0151 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-37-12888A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384660 | ||||||
| chr8:27384746
|
G | A | 4 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(1): Show | 4 | HG02572.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-12802G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384746 | ||||||
| chr8:27384761
|
G | A | 1 | a0002c0006t0001g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-37-12787G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384761 | ||||||
| chr8:27385076
|
G | C | 18 | a0001c0002t0001g0005a0001c0002t0001g0077a0001c0002t0001g0119others(15): Show | 18 | HG01496.hp1 HG01943.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-37-12472G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385076 | ||||||
| chr8:27385088
|
G | A | 1 | a0002c0004t0002g0108 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-37-12460G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385088 | ||||||
| chr8:27385105
|
T | A | 114 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(111): Show | 118 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-37-12443T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385105 | ||||||
| chr8:27385136
|
T | G | 2 | a0001c0001t0003g0029a0001c0001t0003g0034 | 2 | HG01934.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-37-12412T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385136 | ||||||
| chr8:27385363
|
A | G | 2 | a0002c0003t0002g0257a0002c0003t0002g0299 | 2 | HG02004.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-37-12185A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385363 | ||||||
| chr8:27385391
|
G | C | 1 | a0002c0005t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-37-12157G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385391 | ||||||
| chr8:27385452
|
A | G | 1 | a0001c0001t0003g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-37-12096A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385452 | ||||||
| chr8:27385482
|
T | C | 1 | a0001c0009t0002g0313 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-37-12066T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385482 | ||||||
| chr8:27385533
|
C | G | 2 | a0001c0008t0003g0114a0002c0006t0001g0010 | 2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-37-12015C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385533 | ||||||
| chr8:27385557
|
C | T | 30 | a0001c0001t0003g0021a0001c0001t0003g0035a0001c0001t0003g0037others(27): Show | 30 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.-37-11991C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385557 | ||||||
| chr8:27385578
|
A | G | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-37-11970A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385578 | ||||||
| chr8:27385579
|
T | C | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-37-11969T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385579 | ||||||
| chr8:27385621
|
G | T | 6 | a0001c0001t0003g0276a0001c0007t0003g0277a0001c0007t0003g0278others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-11927G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385621 | ||||||
| chr8:27385669
|
G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-37-11879G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385669 | ||||||
| chr8:27385730
|
TAA | T | 6 | a0001c0001t0003g0276a0001c0007t0003g0277a0001c0007t0003g0278others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-11814_-37-1181 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27385730 | |||||
| chr8:27385892
|
C | CA | 215 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(212): Show | 220 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.-37-11637dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27385892 | |||||
| chr8:27385892
|
CA | C | 8 | a0001c0011t0001g0078a0001c0011t0001g0098a0001c0011t0001g0142others(5): Show | 8 | HG01192.hp1 HG01361.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-11637delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27385892 | |||||
| chr8:27385918
|
A | G | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-11630A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385918 | ||||||
| chr8:27385919
|
T | C | 1 | a0001c0007t0003g0137 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-37-11629T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385919 | ||||||
| chr8:27385920
|
C | T | 1 | a0001c0007t0003g0137 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-37-11628C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385920 | ||||||
| chr8:27386078
|
G | A | 6 | a0001c0001t0003g0276a0001c0007t0003g0277a0001c0007t0003g0278others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-11470G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386078 | ||||||
| chr8:27386085
|
T | C | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-11463T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386085 | ||||||
| chr8:27386199
|
C | T | 107 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(104): Show | 108 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-37-11349C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386199 | ||||||
| chr8:27386419
|
A | C | 3 | a0002c0003t0002g0236a0002c0003t0002g0256a0002c0003t0002g0321 | 3 | HG02258.hp2 HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-37-11129A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386419 | ||||||
| chr8:27386440
|
G | C | 1 | a0002c0003t0002g0283 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-37-11108G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386440 | ||||||
| chr8:27386565
|
C | G | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-37-10983C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386565 | ||||||
| chr8:27386783
|
A | G | 114 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(111): Show | 118 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-37-10765A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386783 | ||||||
| chr8:27386795
|
G | A | 1 | a0002c0006t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-37-10753G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386795 | ||||||
| chr8:27386879
|
GT | G | 6 | a0001c0007t0003g0277a0001c0007t0003g0278a0001c0021t0004g0009others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-10656delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27386879 | |||||
| chr8:27386956
|
A | G | 1 | a0001c0002t0001g0176 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-37-10592A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386956 | ||||||
| chr8:27387117
|
C | T | 5 | a0002c0006t0001g0006a0002c0006t0001g0234a0002c0006t0001g0282others(2): Show | 5 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-10431C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387117 | ||||||
| chr8:27387156
|
C | T | 1 | a0002c0006t0001g0286 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-37-10392C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387156 | ||||||
| chr8:27387205
|
A | G | 114 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(111): Show | 118 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-37-10343A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387205 | ||||||
| chr8:27387273
|
C | T | 3 | a0001c0002t0001g0174a0001c0007t0003g0177a0006c0028t0001g0179 | 3 | HG02647.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-37-10275C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387273 | ||||||
| chr8:27387402
|
C | T | 102 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(99): Show | 106 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-37-10146C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387402 | ||||||
| chr8:27387458
|
G | A | 4 | a0001c0001t0003g0276a0001c0007t0003g0279a0001c0007t0003g0280others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-10090G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387458 | ||||||
| chr8:27387566
|
C | T | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-9982C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387566 | ||||||
| chr8:27387739
|
A | T | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-9809A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387739 | ||||||
| chr8:27387817
|
CT | C | 124 | a0001c0002t0001g0145a0001c0002t0001g0158a0001c0002t0001g0171others(121): Show | 128 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.-37-9716delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27387817 | |||||
| chr8:27387901
|
T | C | 1 | a0002c0006t0001g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-37-9647T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387901 | ||||||
| chr8:27388029
|
C | T | 1 | a0001c0010t0003g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-37-9519C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388029 | ||||||
| chr8:27388204
|
A | C | 93 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(90): Show | 95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-37-9344A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388204 | ||||||
| chr8:27388263
|
A | G | 1 | a0002c0006t0001g0286 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-37-9285A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388263 | ||||||
| chr8:27388273
|
C | T | 93 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(90): Show | 95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-37-9275C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388273 | ||||||
| chr8:27388300
|
A | G | 6 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0175others(3): Show | 6 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-9248A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388300 | ||||||
| chr8:27388625
|
A | G | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-37-8923A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388625 | ||||||
| chr8:27388788
|
C | G | 4 | a0001c0007t0003g0135a0001c0007t0003g0136a0001c0007t0003g0137others(1): Show | 4 | HG00735.hp2 HG01993.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-8760C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388788 | ||||||
| chr8:27388820
|
T | C | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.-37-8728T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388820 | ||||||
| chr8:27388916
|
A | G | 8 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-8632A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388916 | ||||||
| chr8:27389028
|
A | T | 1 | a0001c0001t0003g0022 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-37-8520A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389028 | ||||||
| chr8:27389099
|
G | A | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-8449G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389099 | ||||||
| chr8:27389123
|
G | A | 1 | a0002c0003t0002g0069 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-37-8425G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389123 | ||||||
| chr8:27389149
|
C | CTT | 5 | a0002c0006t0001g0006a0002c0006t0001g0234a0002c0006t0001g0282others(2): Show | 5 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-8395_-37-8394d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27389149 | |||||
| chr8:27389177
|
G | C | 3 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115 | 3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-8371G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389177 | ||||||
| chr8:27389179
|
G | A | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-8369G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389179 | ||||||
| chr8:27389232
|
C | T | 1 | a0001c0001t0003g0073 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-37-8316C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389232 | ||||||
| chr8:27389261
|
G | A | 4 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0032others(1): Show | 4 | HG01109.hp2 HG01255.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-8287G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389261 | ||||||
| chr8:27389311
|
AGGAAGAC others(5): Show |
A | 1 | a0002c0004t0002g0112 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-37-8225_-37-8214d others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27389311 | |||||
| chr8:27389313
|
G | A | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-8235G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389313 | ||||||
| chr8:27389331
|
A | C | 106 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(103): Show | 107 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-37-8217A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389331 | ||||||
| chr8:27389492
|
G | T | 1 | a0002c0003t0002g0260 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-37-8056G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389492 | ||||||
| chr8:27389547
|
C | T | 20 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0183others(17): Show | 20 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-37-8001C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389547 | ||||||
| chr8:27389559
|
C | G | 1 | a0002c0004t0002g0209 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-37-7989C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389559 | ||||||
| chr8:27389613
|
G | A | 1 | a0002c0004t0002g0250 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-37-7935G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389613 | ||||||
| chr8:27389781
|
T | C | 6 | a0001c0001t0003g0276a0001c0007t0003g0277a0001c0007t0003g0278others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-7767T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389781 | ||||||
| chr8:27389822
|
G | A | 93 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(90): Show | 95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-37-7726G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389822 | ||||||
| chr8:27390069
|
T | C | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-7479T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390069 | ||||||
| chr8:27390130
|
T | C | 114 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(111): Show | 118 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-37-7418T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390130 | ||||||
| chr8:27390138
|
C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-7410C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390138 | ||||||
| chr8:27390145
|
G | C | 93 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(90): Show | 95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-37-7403G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390145 | ||||||
| chr8:27390168
|
G | T | 1 | a0002c0004t0002g0099 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-37-7380G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390168 | ||||||
| chr8:27390263
|
C | T | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-7285C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390263 | ||||||
| chr8:27390265
|
C | T | 9 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-7283C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390265 | ||||||
| chr8:27390303
|
G | T | 106 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(103): Show | 107 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-37-7245G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390303 | ||||||
| chr8:27390343
|
C | A | 12 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(9): Show | 12 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-37-7205C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390343 | ||||||
| chr8:27390438
|
C | G | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-7110C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390438 | ||||||
| chr8:27390502
|
A | T | 93 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(90): Show | 95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-37-7046A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390502 | ||||||
| chr8:27390510
|
A | C | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-7038A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390510 | ||||||
| chr8:27390515
|
C | A | 1 | a0002c0004t0002g0141 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-37-7033C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390515 | ||||||
| chr8:27390647
|
T | A | 114 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(111): Show | 118 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-37-6901T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390647 | ||||||
| chr8:27390743
|
T | C | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-6805T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390743 | ||||||
| chr8:27390879
|
ACAACGGG others(7): Show |
A | 3 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115 | 3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-6666_-37-6653d others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27390879 | |||||
| chr8:27390918
|
T | C | 245 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(242): Show | 250 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-37-6630T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390918 | ||||||
| chr8:27391044
|
G | T | 244 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(241): Show | 249 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.-37-6504G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391044 | ||||||
| chr8:27391056
|
T | A | 108 | a0001c0008t0003g0114a0001c0009t0002g0018a0001c0009t0002g0087others(105): Show | 112 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-37-6492T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391056 | ||||||
| chr8:27391080
|
C | CT | 19 | a0001c0002t0001g0079a0001c0002t0001g0117a0001c0002t0001g0118others(16): Show | 19 | HG00544.hp2 HG01928.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-6454dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27391080 | |||||
| chr8:27391080
|
CT | C | 241 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(238): Show | 246 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.-37-6454delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27391080 | |||||
| chr8:27391124
|
A | G | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-6424A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391124 | ||||||
| chr8:27391138
|
TGGTGCAA others(9): Show |
T | 5 | a0002c0006t0001g0006a0002c0006t0001g0234a0002c0006t0001g0282others(2): Show | 5 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-6393_-37-6378d others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27391138 | |||||
| chr8:27391150
|
G | A | 102 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(99): Show | 106 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-37-6398G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391150 | ||||||
| chr8:27391154
|
C | T | 23 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0183others(20): Show | 23 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-37-6394C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391154 | ||||||
| chr8:27391189
|
C | T | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-6359C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391189 | ||||||
| chr8:27391221
|
C | T | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-6327C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391221 | ||||||
| chr8:27391245
|
T | C | 112 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(109): Show | 116 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-37-6303T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391245 | ||||||
| chr8:27391292
|
T | C | 20 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0183others(17): Show | 20 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-37-6256T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391292 | ||||||
| chr8:27391377
|
G | A | 1 | a0001c0001t0003g0051 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-37-6171G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391377 | ||||||
| chr8:27391468
|
G | C | 11 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0027others(8): Show | 11 | HG01074.hp1 HG01109.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-6080G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391468 | ||||||
| chr8:27391560
|
T | C | 6 | a0001c0001t0003g0276a0001c0007t0003g0277a0001c0007t0003g0278others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-5988T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391560 | ||||||
| chr8:27391605
|
G | C | 9 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-5943G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391605 | ||||||
| chr8:27391811
|
G | C | 106 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(103): Show | 110 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.-37-5737G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391811 | ||||||
| chr8:27391941
|
A | G | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.-37-5607A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391941 | ||||||
| chr8:27392009
|
C | T | 1 | a0002c0006t0001g0287 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-37-5539C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27392009 | ||||||
| chr8:27392119
|
G | A | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-5429G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27392119 | ||||||
| chr8:27392310
|
C | CT | 38 | a0001c0001t0003g0042a0001c0001t0003g0054a0001c0001t0003g0081others(35): Show | 40 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-37-5222dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27392310 | |||||
| chr8:27392310
|
CT | C | 11 | a0001c0002t0001g0079a0001c0002t0001g0296a0001c0008t0003g0243others(8): Show | 11 | HG01070.hp1 HG01099.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-5222delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27392310 | |||||
| chr8:27392312
|
T | G | 1 | a0001c0002t0001g0206 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-37-5236T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27392312 | ||||||
| chr8:27392472
|
T | C | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-5076T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27392472 | ||||||
| chr8:27392592
|
G | C | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-4956G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27392592 | ||||||
| chr8:27392889
|
C | T | 4 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(1): Show | 4 | HG02572.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-4659C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27392889 | ||||||
| chr8:27393023
|
C | T | 7 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(4): Show | 7 | HG00639.hp1 HG00733.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-4525C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393023 | ||||||
| chr8:27393024
|
G | A | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-4524G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393024 | ||||||
| chr8:27393188
|
C | T | 1 | a0001c0002t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-37-4360C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393188 | ||||||
| chr8:27393304
|
T | C | 114 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(111): Show | 118 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-37-4244T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393304 | ||||||
| chr8:27393314
|
G | A | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-37-4234G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393314 | ||||||
| chr8:27393338
|
G | C | 7 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0175others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-4210G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393338 | ||||||
| chr8:27393416
|
G | A | 104 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(101): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-37-4132G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393416 | ||||||
| chr8:27393534
|
T | C | 93 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(90): Show | 95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-37-4014T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393534 | ||||||
| chr8:27393545
|
A | G | 2 | a0002c0003t0002g0267a0002c0003t0002g0269 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-37-4003A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393545 | ||||||
| chr8:27393728
|
G | C | 4 | a0001c0008t0003g0114a0001c0030t0002g0007a0002c0006t0001g0010others(1): Show | 4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-3820G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393728 | ||||||
| chr8:27393808
|
A | G | 115 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(112): Show | 116 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-37-3740A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393808 | ||||||
| chr8:27394029
|
G | C | 106 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(103): Show | 110 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.-37-3519G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394029 | ||||||
| chr8:27394112
|
G | A | 3 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115 | 3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-3436G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394112 | ||||||
| chr8:27394208
|
G | A | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-3340G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394208 | ||||||
| chr8:27394259
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-37-3289T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394259 | ||||||
| chr8:27394340
|
A | G | 7 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0175others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-3208A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394340 | ||||||
| chr8:27394352
|
A | G | 9 | a0001c0002t0001g0144a0001c0002t0001g0155a0001c0002t0001g0158others(6): Show | 9 | HG00544.hp2 HG02015.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37-3196A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394352 | ||||||
| chr8:27394516
|
G | A | 8 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-3032G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394516 | ||||||
| chr8:27394529
|
G | A | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-37-3019G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394529 | ||||||
| chr8:27394550
|
G | A | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-2998G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394550 | ||||||
| chr8:27394551
|
T | C | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-37-2997T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394551 | ||||||
| chr8:27394603
|
C | T | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-2945C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394603 | ||||||
| chr8:27394678
|
T | G | 1 | a0002c0004t0002g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-37-2870T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394678 | ||||||
| chr8:27394926
|
C | T | 1 | a0001c0001t0003g0029 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-37-2622C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394926 | ||||||
| chr8:27395001
|
G | A | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-2547G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395001 | ||||||
| chr8:27395031
|
C | T | 112 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(109): Show | 116 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-37-2517C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395031 | ||||||
| chr8:27395041
|
C | T | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-2507C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395041 | ||||||
| chr8:27395067
|
C | CT | 7 | a0001c0010t0003g0289a0001c0012t0004g0053a0001c0012t0004g0057others(4): Show | 7 | HG00735.hp1 HG01081.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-2471dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27395067 | |||||
| chr8:27395089
|
G | A | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-2459G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395089 | ||||||
| chr8:27395116
|
T | C | 106 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(103): Show | 110 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.-37-2432T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395116 | ||||||
| chr8:27395229
|
G | C | 102 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(99): Show | 106 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-37-2319G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395229 | ||||||
| chr8:27395234
|
G | A | 1 | a0001c0002t0001g0168 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-37-2314G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395234 | ||||||
| chr8:27395364
|
G | A | 103 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(100): Show | 107 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-37-2184G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395364 | ||||||
| chr8:27395446
|
T | G | 2 | a0001c0002t0001g0171a0001c0002t0001g0172 | 2 | NA18981.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-37-2102T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395446 | ||||||
| chr8:27395475
|
T | A | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-2073T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395475 | ||||||
| chr8:27395492
|
G | C | 9 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-2056G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395492 | ||||||
| chr8:27395596
|
A | G | 2 | a0002c0003t0002g0223a0002c0003t0002g0311 | 2 | NA18961.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-37-1952A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395596 | ||||||
| chr8:27395665
|
T | C | 9 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-1883T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395665 | ||||||
| chr8:27395699
|
G | A | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-1849G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395699 | ||||||
| chr8:27395838
|
A | T | 1 | a0002c0006t0001g0291 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-37-1710A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395838 | ||||||
| chr8:27395880
|
C | T | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-1668C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395880 | ||||||
| chr8:27396060
|
T | C | 244 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(241): Show | 249 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.-37-1488T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396060 | ||||||
| chr8:27396156
|
T | G | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-1392T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396156 | ||||||
| chr8:27396315
|
C | A | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-1233C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396315 | ||||||
| chr8:27396342
|
C | G | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-1206C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396342 | ||||||
| chr8:27396396
|
A | C | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-1152A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396396 | ||||||
| chr8:27396418
|
A | G | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-1130A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396418 | ||||||
| chr8:27396419
|
T | C | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-1129T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396419 | ||||||
| chr8:27396434
|
G | A | 102 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(99): Show | 106 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-37-1114G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396434 | ||||||
| chr8:27396459
|
G | A | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-1089G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396459 | ||||||
| chr8:27396596
|
T | G | 108 | a0001c0008t0003g0114a0001c0009t0002g0018a0001c0009t0002g0087others(105): Show | 112 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-37-952T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396596 | ||||||
| chr8:27396627
|
T | C | 245 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(242): Show | 250 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-37-921T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396627 | ||||||
| chr8:27396890
|
G | A | 1 | a0001c0002t0001g0147 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-37-658G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396890 | ||||||
| chr8:27397078
|
C | T | 1 | a0002c0003t0002g0222 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-37-470C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397078 | ||||||
| chr8:27397079
|
G | A | 9 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-469G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397079 | ||||||
| chr8:27397119
|
C | T | 93 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(90): Show | 95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-37-429C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397119 | ||||||
| chr8:27397121
|
C | T | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-427C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397121 | ||||||
| chr8:27397207
|
C | T | 1 | a0001c0001t0003g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-37-341C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397207 | ||||||
| chr8:27397262
|
G | A | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-286G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397262 | ||||||
| chr8:27397443
|
G | A | 1 | a0001c0002t0001g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-37-105G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397443 | ||||||
| chr8:27397486
|
G | A | 102 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(99): Show | 106 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-37-62G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397486 | ||||||
| chr8:27397808
|
C | T | 104 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(101): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.204+20C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27397808 | ||||||
| chr8:27397851
|
AGCAGCTC others(12): Show |
A | 93 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(90): Show | 95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.204+74_204+92delTG others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27397851 | |||||
| chr8:27397899
|
G | C | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.204+111G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27397899 | ||||||
| chr8:27398032
|
G | T | 1 | a0001c0001t0003g0318 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.204+244G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398032 | ||||||
| chr8:27398118
|
A | G | 104 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(101): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.204+330A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398118 | ||||||
| chr8:27398228
|
T | G | 1 | a0001c0011t0001g0148 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.204+440T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398228 | ||||||
| chr8:27398363
|
G | A | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.204+575G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398363 | ||||||
| chr8:27398474
|
C | T | 1 | a0002c0003t0002g0260 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.204+686C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398474 | ||||||
| chr8:27398568
|
A | C | 1 | a0001c0001t0003g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.204+780A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398568 | ||||||
| chr8:27398746
|
T | C | 106 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(103): Show | 110 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.204+958T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398746 | ||||||
| chr8:27398797
|
C | G | 244 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(241): Show | 249 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.204+1009C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398797 | ||||||
| chr8:27398842
|
G | A | 102 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(99): Show | 106 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.204+1054G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398842 | ||||||
| chr8:27398900
|
C | T | 7 | a0001c0001t0003g0178a0001c0001t0003g0294a0001c0007t0003g0303others(4): Show | 7 | HG00639.hp1 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+1112C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398900 | ||||||
| chr8:27398931
|
C | T | 9 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+1143C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398931 | ||||||
| chr8:27399193
|
C | T | 2 | a0001c0030t0002g0007a0002c0006t0002g0317 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.204+1405C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399193 | ||||||
| chr8:27399352
|
A | G | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+1564A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399352 | ||||||
| chr8:27399401
|
G | A | 93 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(90): Show | 95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.204+1613G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399401 | ||||||
| chr8:27399487
|
G | A | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+1699G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399487 | ||||||
| chr8:27399529
|
A | G | 104 | a0001c0009t0002g0018a0001c0009t0002g0087a0001c0009t0002g0103others(101): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.204+1741A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399529 | ||||||
| chr8:27399569
|
A | G | 9 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+1781A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399569 | ||||||
| chr8:27399572
|
T | G | 3 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115 | 3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.204+1784T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399572 | ||||||
| chr8:27399576
|
C | G | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+1788C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399576 | ||||||
| chr8:27399628
|
A | G | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.204+1840A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399628 | ||||||
| chr8:27399680
|
G | C | 1 | a0001c0001t0003g0196 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.204+1892G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399680 | ||||||
| chr8:27400103
|
A | G | 1 | a0001c0002t0001g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.204+2315A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400103 | ||||||
| chr8:27400270
|
T | G | 120 | a0001c0001t0003g0276a0001c0002t0001g0296a0001c0007t0003g0277others(117): Show | 124 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.204+2482T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400270 | ||||||
| chr8:27400376
|
C | T | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.204+2588C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400376 | ||||||
| chr8:27400377
|
T | C | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.204+2589T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400377 | ||||||
| chr8:27400386
|
G | A | 4 | a0002c0006t0001g0006a0002c0006t0001g0234a0002c0006t0001g0290others(1): Show | 4 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+2598G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400386 | ||||||
| chr8:27400447
|
TA | T | 139 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(136): Show | 142 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.204+2676delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27400447 | |||||
| chr8:27400448
|
A | T | 1 | a0002c0004t0002g0242 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.204+2660A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400448 | ||||||
| chr8:27400569
|
G | A | 113 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(110): Show | 117 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.204+2781G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400569 | ||||||
| chr8:27400581
|
A | T | 3 | a0001c0010t0003g0289a0001c0021t0004g0009a0001c0022t0002g0008 | 3 | HG03225.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.204+2793A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400581 | ||||||
| chr8:27400637
|
G | A | 1 | a0002c0003t0002g0260 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.204+2849G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400637 | ||||||
| chr8:27400678
|
G | A | 111 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(108): Show | 115 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.204+2890G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400678 | ||||||
| chr8:27400732
|
A | G | 111 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(108): Show | 115 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.204+2944A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400732 | ||||||
| chr8:27400743
|
T | A | 1 | a0002c0005t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.204+2955T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400743 | ||||||
| chr8:27400790
|
G | A | 1 | a0002c0003t0002g0299 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.204+3002G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400790 | ||||||
| chr8:27400796
|
G | A | 111 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(108): Show | 115 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.204+3008G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400796 | ||||||
| chr8:27400859
|
A | T | 3 | a0001c0010t0003g0289a0001c0021t0004g0009a0001c0022t0002g0008 | 3 | HG03225.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.204+3071A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400859 | ||||||
| chr8:27400878
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.204+3090G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400878 | ||||||
| chr8:27400940
|
G | A | 1 | a0001c0001t0003g0025 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.204+3152G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400940 | ||||||
| chr8:27400959
|
A | G | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.204+3171A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400959 | ||||||
| chr8:27400976
|
T | C | 10 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(7): Show | 10 | HG00639.hp1 HG00733.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+3188T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400976 | ||||||
| chr8:27400981
|
A | ACCAAAAG others(1): Show |
111 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(108): Show | 115 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.204+3199_204+3200i others(10): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27400981 | |||||
| chr8:27401011
|
C | A | 3 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115 | 3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.204+3223C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401011 | ||||||
| chr8:27401117
|
T | C | 131 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0183others(128): Show | 135 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.204+3329T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401117 | ||||||
| chr8:27401141
|
A | AAAAC | 111 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(108): Show | 115 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.204+3357_204+3360d others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27401141 | |||||
| chr8:27401151
|
G | C | 1 | a0002c0003t0002g0219 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.204+3363G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401151 | ||||||
| chr8:27401260
|
AGAGAACC others(2): Show |
A | 115 | a0001c0001t0003g0051a0001c0002t0001g0296a0001c0008t0003g0114others(112): Show | 119 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.204+3488_204+3496d others(11): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27401260 | |||||
| chr8:27401589
|
C | T | 2 | a0001c0007t0003g0277a0001c0007t0003g0278 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.204+3801C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401589 | ||||||
| chr8:27401634
|
A | T | 111 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(108): Show | 115 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.204+3846A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401634 | ||||||
| chr8:27401645
|
A | G | 20 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0183others(17): Show | 20 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+3857A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401645 | ||||||
| chr8:27401713
|
A | C | 111 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(108): Show | 115 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.204+3925A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401713 | ||||||
| chr8:27401909
|
A | G | 234 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(231): Show | 239 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.204+4121A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401909 | ||||||
| chr8:27402036
|
T | C | 10 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(7): Show | 10 | HG00639.hp1 HG00733.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+4248T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402036 | ||||||
| chr8:27402157
|
G | A | 9 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+4369G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402157 | ||||||
| chr8:27402174
|
G | A | 2 | a0002c0006t0001g0286a0002c0006t0001g0287 | 2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.204+4386G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402174 | ||||||
| chr8:27402232
|
C | T | 6 | a0001c0001t0003g0276a0001c0007t0003g0277a0001c0007t0003g0278others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+4444C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402232 | ||||||
| chr8:27402305
|
G | A | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+4517G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402305 | ||||||
| chr8:27402398
|
C | T | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+4610C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402398 | ||||||
| chr8:27402416
|
A | T | 84 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(81): Show | 85 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.204+4628A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402416 | ||||||
| chr8:27402458
|
G | A | 4 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(1): Show | 4 | HG02572.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+4670G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402458 | ||||||
| chr8:27402656
|
G | A | 2 | a0001c0021t0004g0009a0001c0022t0002g0008 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.204+4868G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402656 | ||||||
| chr8:27402764
|
A | G | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.204+4976A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402764 | ||||||
| chr8:27402887
|
T | G | 18 | a0001c0001t0003g0276a0001c0007t0003g0277a0001c0007t0003g0278others(15): Show | 20 | HG00609.hp2 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+5099T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402887 | ||||||
| chr8:27402889
|
C | T | 1 | a0001c0002t0001g0160 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.204+5101C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402889 | ||||||
| chr8:27402967
|
A | G | 107 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(104): Show | 108 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.204+5179A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402967 | ||||||
| chr8:27403055
|
C | G | 6 | a0001c0001t0003g0276a0001c0007t0003g0277a0001c0007t0003g0278others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+5267C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403055 | ||||||
| chr8:27403120
|
G | A | 11 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(8): Show | 13 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.204+5332G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403120 | ||||||
| chr8:27403265
|
C | T | 1 | a0001c0001t0005g0060 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.204+5477C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403265 | ||||||
| chr8:27403294
|
T | C | 5 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(2): Show | 5 | HG00544.hp1 HG00609.hp1 HG00673.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+5506T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403294 | ||||||
| chr8:27403296
|
G | A | 2 | a0001c0001t0003g0029a0001c0001t0003g0034 | 2 | HG01934.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.204+5508G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403296 | ||||||
| chr8:27403310
|
A | C | 9 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(6): Show | 9 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.204+5522A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403310 | ||||||
| chr8:27403318
|
C | T | 1 | a0001c0010t0003g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.204+5530C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403318 | ||||||
| chr8:27403329
|
A | G | 3 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115 | 3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.204+5541A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403329 | ||||||
| chr8:27403338
|
ACATAGTT others(4): Show |
A | 9 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(6): Show | 9 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.204+5554_204+5564d others(13): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27403338 | |||||
| chr8:27403378
|
G | T | 3 | a0001c0002t0001g0140a0001c0002t0001g0162a0002c0006t0001g0213 | 3 | NA18955.hp1 NA19056.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.204+5590G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403378 | ||||||
| chr8:27403408
|
C | T | 9 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+5620C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403408 | ||||||
| chr8:27403431
|
T | C | 20 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0183others(17): Show | 20 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+5643T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403431 | ||||||
| chr8:27403461
|
G | A | 1 | a0001c0001t0003g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.204+5673G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403461 | ||||||
| chr8:27403540
|
G | T | 7 | a0001c0011t0001g0078a0001c0011t0001g0098a0001c0011t0001g0142others(4): Show | 7 | HG01192.hp1 HG01361.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+5752G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403540 | ||||||
| chr8:27403609
|
G | A | 3 | a0001c0002t0001g0119a0001c0002t0001g0121a0001c0002t0001g0122 | 3 | NA18957.hp2 NA18969.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.204+5821G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403609 | ||||||
| chr8:27403621
|
C | G | 9 | a0002c0003t0002g0247a0002c0004t0002g0224a0002c0004t0002g0225others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.204+5833C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403621 | ||||||
| chr8:27403718
|
C | T | 1 | a0001c0002t0001g0080 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.204+5930C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403718 | ||||||
| chr8:27403740
|
CT | C | 8 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+5955delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27403740 | |||||
| chr8:27403748
|
C | T | 6 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0175others(3): Show | 6 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+5960C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403748 | ||||||
| chr8:27403749
|
TTGC | T | 118 | a0001c0001t0003g0022a0001c0001t0003g0178a0001c0001t0003g0276others(115): Show | 120 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.204+5981_204+5983d others(5): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27403749 | |||||
| chr8:27403766
|
GCTGCTC | G | 9 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+5981_204+5986d others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27403766 | |||||
| chr8:27403788
|
T | C | 9 | a0001c0009t0002g0125a0001c0009t0002g0310a0001c0009t0002g0313others(6): Show | 11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+6000T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403788 | ||||||
| chr8:27403801
|
G | C | 1 | a0009c0019t0002g0102 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.204+6013G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403801 | ||||||
| chr8:27403904
|
C | G | 1 | a0001c0002t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.204+6116C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403904 | ||||||
| chr8:27403974
|
A | C | 5 | a0002c0006t0001g0006a0002c0006t0001g0234a0002c0006t0001g0282others(2): Show | 5 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+6186A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403974 | ||||||
| chr8:27404017
|
T | C | 2 | a0001c0002t0001g0235a0001c0010t0003g0289 | 2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.204+6229T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404017 | ||||||
| chr8:27404023
|
C | G | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.204+6235C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404023 | ||||||
| chr8:27404039
|
CCA | C | 92 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(89): Show | 93 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.204+6252_204+6253d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404039 | ||||||
| chr8:27404180
|
C | T | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.204+6392C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404180 | ||||||
| chr8:27404298
|
A | G | 239 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(236): Show | 244 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.204+6510A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404298 | ||||||
| chr8:27404424
|
C | T | 14 | a0001c0001t0003g0178a0001c0001t0003g0294a0001c0002t0001g0173others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.204+6636C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404424 | ||||||
| chr8:27404461
|
C | T | 4 | a0001c0007t0003g0135a0001c0007t0003g0136a0001c0007t0003g0137others(1): Show | 4 | HG00735.hp2 HG01993.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+6673C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404461 | ||||||
| chr8:27404620
|
C | T | 1 | a0001c0002t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.204+6832C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404620 | ||||||
| chr8:27404670
|
A | G | 1 | a0001c0007t0003g0189 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.204+6882A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404670 | ||||||
| chr8:27404678
|
C | T | 155 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(152): Show | 159 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.204+6890C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404678 | ||||||
| chr8:27404782
|
A | G | 7 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0183others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+6994A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404782 | ||||||
| chr8:27404827
|
G | C | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.204+7039G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404827 | ||||||
| chr8:27404849
|
C | G | 106 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(103): Show | 107 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.204+7061C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404849 | ||||||
| chr8:27405017
|
C | CCTTCCTC others(7): Show |
1 | a0001c0009t0002g0018 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.204+7240_204+7253d others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405017 | |||||
| chr8:27405035
|
C | CCT | 15 | a0001c0002t0001g0157a0001c0002t0001g0161a0001c0002t0001g0164others(12): Show | 15 | HG00423.hp1 HG00609.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.204+7280_204+7281d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCT | 5 | a0001c0002t0001g0079a0001c0002t0001g0124a0001c0002t0001g0163others(2): Show | 5 | HG00323.hp1 HG01884.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+7278_204+7281d others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCTCT | 5 | a0001c0001t0003g0113a0001c0001t0003g0115a0001c0001t0003g0288others(2): Show | 5 | HG02559.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+7276_204+7281d others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCTCTC others(1): Show |
3 | a0002c0005t0001g0026a0002c0005t0001g0031a0002c0005t0001g0033 | 3 | HG01928.hp1 HG01943.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.204+7274_204+7281d others(10): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCTCTC others(3): Show |
2 | a0001c0001t0003g0088a0001c0002t0001g0226 | 2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.204+7272_204+7281d others(12): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCTCTC others(5): Show |
5 | a0001c0001t0003g0024a0001c0001t0003g0029a0001c0001t0003g0066others(2): Show | 5 | HG01934.hp1 HG02280.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+7270_204+7281d others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCTCTC others(7): Show |
12 | a0001c0001t0003g0032a0001c0001t0003g0035a0001c0001t0003g0071others(9): Show | 12 | HG00544.hp1 HG00609.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.204+7268_204+7281d others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCTCTC others(9): Show |
14 | a0001c0001t0003g0034a0001c0001t0003g0064a0001c0001t0003g0082others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.204+7266_204+7281d others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCTCTC others(11): Show |
22 | a0001c0001t0003g0021a0001c0001t0003g0027a0001c0001t0003g0028others(19): Show | 22 | HG00323.hp2 HG00621.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.204+7264_204+7281d others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCTCTC others(13): Show |
12 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0051others(9): Show | 12 | HG00673.hp1 HG01169.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.204+7262_204+7281d others(22): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCTCTC others(15): Show |
12 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0025others(9): Show | 12 | HG00408.hp1 HG01074.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.204+7260_204+7281d others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCTCTC others(17): Show |
6 | a0001c0001t0003g0037a0001c0001t0003g0183a0001c0001t0003g0185others(3): Show | 7 | HG00438.hp1 HG00639.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.204+7258_204+7281d others(26): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCTCTC others(19): Show |
6 | a0001c0001t0003g0015a0001c0001t0003g0090a0001c0001t0003g0093others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+7256_204+7281d others(28): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCTCTC others(21): Show |
1 | a0001c0001t0003g0181 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.204+7254_204+7281d others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CCTCTCTC others(23): Show |
2 | a0001c0001t0003g0184a0002c0005t0001g0197 | 2 | HG01123.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.204+7252_204+7281d others(32): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
C | CTCTCTCT others(12): Show |
1 | a0001c0001t0003g0049 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.204+7247_204+7248i others(21): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405035 | ||||||
| chr8:27405035
|
CCT | C | 4 | a0001c0002t0001g0131a0001c0002t0001g0296a0001c0008t0003g0295others(1): Show | 4 | HG01433.hp2 HG02145.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+7280_204+7281d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
CCTCTCT | C | 18 | a0001c0008t0003g0243a0001c0008t0003g0292a0001c0008t0003g0315others(15): Show | 18 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.204+7276_204+7281d others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405035
|
CCTCTCTC others(11): Show |
C | 101 | a0001c0001t0003g0022a0001c0008t0003g0114a0001c0009t0002g0103others(98): Show | 103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.204+7264_204+7281d others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | |||||
| chr8:27405069
|
T | TCTCTCTC others(20): Show |
1 | a0001c0001t0003g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.204+7281_204+7282i others(29): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405069 | ||||||
| chr8:27405163
|
C | A | 6 | a0001c0002t0001g0296a0001c0008t0003g0295a0001c0008t0003g0314others(3): Show | 6 | HG02258.hp1 HG02486.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+7375C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405163 | ||||||
| chr8:27405171
|
G | C | 1 | a0001c0002t0001g0155 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.204+7383G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405171 | ||||||
| chr8:27405208
|
C | T | 6 | a0002c0003t0002g0012a0002c0004t0002g0001a0002c0004t0002g0011others(3): Show | 8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+7420C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405208 | ||||||
| chr8:27405291
|
G | A | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.204+7503G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405291 | ||||||
| chr8:27405377
|
C | G | 5 | a0001c0002t0001g0296a0001c0008t0003g0295a0001c0008t0003g0314others(2): Show | 5 | HG02258.hp1 HG02486.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+7589C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405377 | ||||||
| chr8:27405521
|
G | A | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.204+7733G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405521 | ||||||
| chr8:27405590
|
C | T | 71 | a0001c0008t0003g0243a0001c0008t0003g0292a0001c0008t0003g0319others(68): Show | 72 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.204+7802C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405590 | ||||||
| chr8:27405596
|
C | T | 1 | a0001c0009t0002g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.204+7808C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405596 | ||||||
| chr8:27405641
|
G | A | 2 | a0001c0008t0003g0314a0001c0008t0003g0315 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.204+7853G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405641 | ||||||
| chr8:27405657
|
A | G | 39 | a0001c0009t0002g0106a0001c0012t0004g0053a0001c0012t0004g0057others(36): Show | 40 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.204+7869A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405657 | ||||||
| chr8:27405831
|
G | C | 8 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+8043G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405831 | ||||||
| chr8:27405842
|
A | T | 63 | a0001c0009t0002g0103a0001c0012t0004g0030a0001c0012t0004g0211others(60): Show | 64 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.204+8054A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405842 | ||||||
| chr8:27405916
|
G | T | 222 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(219): Show | 227 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.204+8128G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405916 | ||||||
| chr8:27406263
|
CCTTAA | C | 124 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(121): Show | 127 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.204+8481_204+8485d others(7): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27406263 | |||||
| chr8:27406275
|
T | C | 1 | a0001c0011t0001g0098 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.204+8487T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406275 | ||||||
| chr8:27406383
|
C | T | 100 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(97): Show | 101 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.204+8595C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406383 | ||||||
| chr8:27406393
|
A | C | 6 | a0002c0003t0002g0012a0002c0004t0002g0001a0002c0004t0002g0011others(3): Show | 8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+8605A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406393 | ||||||
| chr8:27406453
|
T | C | 1 | a0001c0001t0003g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.204+8665T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406453 | ||||||
| chr8:27406463
|
T | C | 8 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+8675T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406463 | ||||||
| chr8:27406593
|
T | C | 232 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(229): Show | 237 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.204+8805T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406593 | ||||||
| chr8:27406728
|
C | A | 100 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(97): Show | 101 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.204+8940C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406728 | ||||||
| chr8:27406824
|
A | G | 2 | a0002c0006t0001g0234a0002c0006t0001g0290 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.204+9036A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406824 | ||||||
| chr8:27406830
|
A | G | 1 | a0002c0005t0001g0002 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.204+9042A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406830 | ||||||
| chr8:27407027
|
C | A | 1 | a0002c0003t0002g0239 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.204+9239C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407027 | ||||||
| chr8:27407038
|
G | T | 4 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+9250G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407038 | ||||||
| chr8:27407150
|
G | A | 319 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(316): Show | 324 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.204+9362G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407150 | ||||||
| chr8:27407159
|
G | A | 229 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(226): Show | 234 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.204+9371G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407159 | ||||||
| chr8:27407364
|
A | G | 1 | a0001c0001t0003g0035 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.204+9576A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407364 | ||||||
| chr8:27407434
|
C | T | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.204+9646C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407434 | ||||||
| chr8:27407435
|
G | A | 67 | a0001c0009t0002g0103a0001c0010t0003g0289a0001c0012t0004g0030others(64): Show | 68 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.204+9647G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407435 | ||||||
| chr8:27407694
|
C | G | 4 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+9906C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407694 | ||||||
| chr8:27407808
|
C | T | 5 | a0001c0007t0003g0277a0001c0007t0003g0278a0001c0007t0003g0279others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+10020C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407808 | ||||||
| chr8:27407854
|
T | C | 118 | a0001c0002t0001g0296a0001c0007t0003g0277a0001c0007t0003g0278others(115): Show | 120 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.204+10066T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407854 | ||||||
| chr8:27407887
|
T | C | 1 | a0001c0002t0001g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.204+10099T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407887 | ||||||
| chr8:27407957
|
A | G | 1 | a0001c0007t0003g0303 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.204+10169A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407957 | ||||||
| chr8:27407959
|
A | G | 46 | a0001c0007t0003g0277a0001c0007t0003g0278a0001c0007t0003g0279others(43): Show | 47 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.204+10171A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407959 | ||||||
| chr8:27408002
|
C | A | 2 | a0001c0001t0003g0028a0001c0001t0003g0032 | 2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.204+10214C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408002 | ||||||
| chr8:27408008
|
T | C | 1 | a0009c0019t0002g0102 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.204+10220T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408008 | ||||||
| chr8:27408152
|
C | T | 1 | a0002c0003t0002g0207 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.204+10364C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408152 | ||||||
| chr8:27408163
|
G | C | 16 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(13): Show | 16 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.204+10375G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408163 | ||||||
| chr8:27408165
|
A | G | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.204+10377A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408165 | ||||||
| chr8:27408190
|
GA | G | 67 | a0001c0009t0002g0103a0001c0010t0003g0289a0001c0012t0004g0030others(64): Show | 68 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.204+10405delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27408190 | |||||
| chr8:27408212
|
C | A | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.204+10424C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408212 | ||||||
| chr8:27408290
|
G | A | 6 | a0002c0003t0002g0012a0002c0004t0002g0001a0002c0004t0002g0011others(3): Show | 8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+10502G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408290 | ||||||
| chr8:27408370
|
A | G | 41 | a0001c0008t0003g0114a0001c0009t0002g0106a0001c0012t0004g0053others(38): Show | 42 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.204+10582A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408370 | ||||||
| chr8:27408595
|
C | T | 1 | a0002c0004t0002g0209 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.204+10807C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408595 | ||||||
| chr8:27408640
|
C | T | 1 | a0002c0003t0002g0247 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.204+10852C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408640 | ||||||
| chr8:27408664
|
C | G | 1 | a0002c0006t0001g0323 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.204+10876C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408664 | ||||||
| chr8:27408770
|
A | T | 40 | a0001c0008t0003g0114a0001c0009t0002g0106a0001c0012t0004g0053others(37): Show | 41 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+10982A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408770 | ||||||
| chr8:27408948
|
T | C | 67 | a0001c0009t0002g0103a0001c0010t0003g0289a0001c0012t0004g0030others(64): Show | 68 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.205-10947T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408948 | ||||||
| chr8:27408987
|
G | A | 1 | a0001c0012t0004g0053 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.205-10908G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408987 | ||||||
| chr8:27409144
|
C | T | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-10751C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27409144 | ||||||
| chr8:27409784
|
C | T | 4 | a0001c0001t0003g0024a0002c0005t0001g0026a0002c0005t0001g0031others(1): Show | 4 | HG01928.hp1 HG01943.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-10111C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27409784 | ||||||
| chr8:27410023
|
A | C | 4 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-9872A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410023 | ||||||
| chr8:27410058
|
A | T | 2 | a0002c0006t0001g0006a0002c0006t0001g0282 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.205-9837A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410058 | ||||||
| chr8:27410079
|
A | G | 6 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-9816A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410079 | ||||||
| chr8:27410089
|
C | G | 4 | a0001c0002t0001g0174a0001c0002t0001g0226a0001c0007t0003g0177others(1): Show | 4 | HG02647.hp2 HG02965.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-9806C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410089 | ||||||
| chr8:27410170
|
C | T | 1 | a0002c0018t0002g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.205-9725C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410170 | ||||||
| chr8:27410359
|
G | GC | 237 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(234): Show | 242 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.205-9534dupC | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27410359 | |||||
| chr8:27410614
|
G | T | 1 | a0002c0003t0002g0262 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.205-9281G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410614 | ||||||
| chr8:27410665
|
A | G | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.205-9230A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410665 | ||||||
| chr8:27410738
|
G | T | 1 | a0002c0004t0002g0104 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.205-9157G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410738 | ||||||
| chr8:27411066
|
A | G | 6 | a0002c0003t0002g0012a0002c0004t0002g0001a0002c0004t0002g0011others(3): Show | 8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-8829A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411066 | ||||||
| chr8:27411099
|
C | T | 75 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(72): Show | 76 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.205-8796C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411099 | ||||||
| chr8:27411113
|
G | A | 8 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-8782G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411113 | ||||||
| chr8:27411171
|
G | T | 44 | a0001c0007t0003g0277a0001c0007t0003g0278a0001c0007t0003g0279others(41): Show | 45 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.205-8724G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411171 | ||||||
| chr8:27411233
|
T | C | 249 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(246): Show | 254 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.205-8662T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411233 | ||||||
| chr8:27411307
|
G | C | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.205-8588G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411307 | ||||||
| chr8:27411396
|
A | G | 1 | a0001c0001t0003g0082 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.205-8499A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411396 | ||||||
| chr8:27411471
|
T | G | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.205-8424T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411471 | ||||||
| chr8:27411636
|
C | T | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-8259C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411636 | ||||||
| chr8:27411654
|
A | G | 8 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-8241A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411654 | ||||||
| chr8:27411899
|
T | C | 112 | a0001c0002t0001g0296a0001c0007t0003g0277a0001c0007t0003g0278others(109): Show | 114 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.205-7996T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411899 | ||||||
| chr8:27412046
|
A | G | 1 | a0001c0001t0003g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.205-7849A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412046 | ||||||
| chr8:27412055
|
C | G | 227 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(224): Show | 232 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.205-7840C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412055 | ||||||
| chr8:27412090
|
G | A | 5 | a0001c0007t0003g0277a0001c0007t0003g0278a0001c0007t0003g0279others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.205-7805G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412090 | ||||||
| chr8:27412130
|
G | A | 238 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(235): Show | 243 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.205-7765G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412130 | ||||||
| chr8:27412161
|
G | GTTGA | 118 | a0001c0002t0001g0296a0001c0007t0003g0277a0001c0007t0003g0278others(115): Show | 120 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.205-7716_205-7713d others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27412161 | |||||
| chr8:27412367
|
G | C | 1 | a0001c0013t0003g0304 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.205-7528G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412367 | ||||||
| chr8:27412367
|
G | T | 232 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(229): Show | 237 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.205-7528G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412367 | ||||||
| chr8:27412597
|
C | G | 1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.205-7298C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412597 | ||||||
| chr8:27412706
|
C | T | 2 | a0002c0005t0001g0198a0002c0005t0001g0199 | 2 | NA19056.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.205-7189C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412706 | ||||||
| chr8:27412899
|
G | C | 238 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(235): Show | 243 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.205-6996G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412899 | ||||||
| chr8:27412900
|
T | G | 114 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(111): Show | 117 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.205-6995T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412900 | ||||||
| chr8:27412909
|
G | A | 226 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(223): Show | 231 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.205-6986G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412909 | ||||||
| chr8:27412966
|
A | T | 238 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(235): Show | 243 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.205-6929A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412966 | ||||||
| chr8:27413031
|
A | T | 1 | a0002c0003t0002g0069 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.205-6864A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413031 | ||||||
| chr8:27413039
|
G | GA | 6 | a0001c0007t0003g0277a0001c0007t0003g0278a0001c0007t0003g0279others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-6844dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27413039 | |||||
| chr8:27413039
|
G | GAAA | 7 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.205-6846_205-6844d others(5): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27413039 | |||||
| chr8:27413039
|
GA | G | 66 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(63): Show | 67 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.205-6844delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27413039 | |||||
| chr8:27413070
|
TA | T | 5 | a0001c0007t0003g0277a0001c0007t0003g0278a0001c0007t0003g0279others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.205-6824delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413070 | ||||||
| chr8:27413241
|
G | A | 3 | a0002c0004t0002g0094a0002c0004t0002g0109a0002c0004t0002g0110 | 3 | HG00741.hp2 HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.205-6654G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413241 | ||||||
| chr8:27413324
|
G | A | 1 | a0001c0001t0003g0196 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.205-6571G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413324 | ||||||
| chr8:27413330
|
A | G | 4 | a0002c0005t0001g0194a0002c0005t0001g0195a0002c0005t0001g0197others(1): Show | 4 | HG01081.hp2 HG01123.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-6565A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413330 | ||||||
| chr8:27413421
|
T | C | 1 | a0001c0010t0003g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.205-6474T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413421 | ||||||
| chr8:27413463
|
G | A | 2 | a0001c0007t0003g0277a0001c0007t0003g0278 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.205-6432G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413463 | ||||||
| chr8:27413553
|
A | T | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.205-6342A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413553 | ||||||
| chr8:27413562
|
C | A | 3 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160 | 3 | HG00544.hp2 NA19074.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.205-6333C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413562 | ||||||
| chr8:27413570
|
T | C | 6 | a0001c0011t0001g0078a0001c0011t0001g0098a0001c0011t0001g0142others(3): Show | 6 | HG01192.hp1 HG02056.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-6325T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413570 | ||||||
| chr8:27413668
|
T | C | 1 | a0001c0010t0003g0230 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.205-6227T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413668 | ||||||
| chr8:27413717
|
T | A | 3 | a0001c0013t0003g0301a0001c0013t0003g0302a0001c0013t0003g0304 | 3 | HG00639.hp1 HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.205-6178T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413717 | ||||||
| chr8:27413725
|
G | A | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.205-6170G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413725 | ||||||
| chr8:27413856
|
A | G | 1 | a0002c0004t0002g0112 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.205-6039A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413856 | ||||||
| chr8:27413988
|
T | G | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.205-5907T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413988 | ||||||
| chr8:27414001
|
A | G | 4 | a0002c0005t0001g0194a0002c0005t0001g0195a0002c0005t0001g0197others(1): Show | 4 | HG01081.hp2 HG01123.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-5894A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414001 | ||||||
| chr8:27414065
|
A | G | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-5830A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414065 | ||||||
| chr8:27414106
|
G | A | 9 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(6): Show | 9 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.205-5789G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414106 | ||||||
| chr8:27414246
|
GCTT | G | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.205-5642_205-5640d others(5): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414246 | |||||
| chr8:27414253
|
CT | C | 226 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(223): Show | 231 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.205-5631delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414253 | |||||
| chr8:27414280
|
T | C | 8 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0007t0003g0303others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-5615T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414280 | ||||||
| chr8:27414340
|
G | T | 1 | a0002c0003t0002g0271 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.205-5555G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414340 | ||||||
| chr8:27414405
|
C | T | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.205-5490C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414405 | ||||||
| chr8:27414493
|
G | A | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-5402G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414493 | ||||||
| chr8:27414528
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.205-5367G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414528 | ||||||
| chr8:27414543
|
G | T | 1 | a0001c0010t0003g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.205-5352G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414543 | ||||||
| chr8:27414588
|
G | A | 1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.205-5307G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414588 | ||||||
| chr8:27414602
|
C | G | 12 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(9): Show | 13 | HG00733.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.205-5293C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414602 | ||||||
| chr8:27414604
|
C | G | 74 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(71): Show | 75 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.205-5291C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414604 | ||||||
| chr8:27414606
|
C | CTCTCTCT others(25): Show |
6 | a0002c0003t0002g0012a0002c0004t0002g0001a0002c0004t0002g0011others(3): Show | 8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-5288_205-5287i others(34): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414606 | |||||
| chr8:27414606
|
C | CTCTCTGT others(21): Show |
3 | a0002c0006t0001g0006a0002c0006t0001g0010a0002c0006t0001g0282 | 3 | HG00738.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.205-5288_205-5287i others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414606 | |||||
| chr8:27414606
|
C | CTCTGTGT others(21): Show |
9 | a0001c0007t0003g0303a0001c0008t0003g0114a0001c0010t0003g0230others(6): Show | 9 | HG02486.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.205-5288_205-5287i others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414606 | |||||
| chr8:27414606
|
C | CTCTGTGT others(23): Show |
1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.205-5288_205-5287i others(32): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414606 | |||||
| chr8:27414606
|
C | G | 90 | a0001c0001t0003g0097a0001c0001t0003g0196a0001c0001t0003g0227others(87): Show | 91 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.205-5289C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414606 | ||||||
| chr8:27414608
|
G | GTGTGTGT others(19): Show |
1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.205-5272_205-5271i others(28): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | |||||
| chr8:27414608
|
G | GTGTGTGT others(21): Show |
143 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(140): Show | 145 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.205-5274_205-5273i others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | |||||
| chr8:27414608
|
G | GTGTGTGT others(23): Show |
68 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0009t0002g0103others(65): Show | 69 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.205-5274_205-5273i others(32): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | |||||
| chr8:27414608
|
G | GTGTGTGT others(25): Show |
2 | a0001c0008t0003g0316a0002c0006t0001g0287 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.205-5274_205-5273i others(34): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | |||||
| chr8:27414608
|
G | GTGTGTGT others(27): Show |
1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.205-5274_205-5273i others(36): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | |||||
| chr8:27414608
|
G | GTGTGTGT others(23): Show |
2 | a0001c0008t0003g0243a0001c0008t0003g0295 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.205-5274_205-5273i others(32): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | |||||
| chr8:27414608
|
G | GTGTGTGT others(21): Show |
1 | a0001c0002t0001g0296 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.205-5274_205-5273i others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | |||||
| chr8:27414608
|
G | T | 19 | a0001c0007t0003g0303a0001c0008t0003g0114a0001c0010t0003g0230others(16): Show | 21 | HG00738.hp1 HG02486.hp1 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.205-5287G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414608 | ||||||
| chr8:27414618
|
G | T | 1 | a0001c0002t0001g0168 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.205-5277G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414618 | ||||||
| chr8:27414781
|
C | G | 5 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0276others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.205-5114C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414781 | ||||||
| chr8:27414843
|
T | C | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.205-5052T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414843 | ||||||
| chr8:27414884
|
G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.205-5011G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414884 | ||||||
| chr8:27414890
|
AC | A | 75 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(72): Show | 76 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.205-5004delC | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414890 | ||||||
| chr8:27415068
|
G | A | 68 | a0001c0009t0002g0103a0001c0010t0003g0289a0001c0012t0004g0030others(65): Show | 69 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.205-4827G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415068 | ||||||
| chr8:27415080
|
TTTTG | T | 6 | a0002c0003t0002g0012a0002c0004t0002g0001a0002c0004t0002g0011others(3): Show | 8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-4803_205-4800d others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27415080 | |||||
| chr8:27415126
|
C | T | 1 | a0001c0002t0001g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.205-4769C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415126 | ||||||
| chr8:27415274
|
G | C | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.205-4621G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415274 | ||||||
| chr8:27415646
|
G | A | 10 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(7): Show | 10 | HG00738.hp1 HG02486.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.205-4249G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415646 | ||||||
| chr8:27415692
|
A | G | 6 | a0001c0011t0001g0078a0001c0011t0001g0098a0001c0011t0001g0142others(3): Show | 6 | HG01192.hp1 HG02056.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-4203A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415692 | ||||||
| chr8:27415783
|
A | G | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.205-4112A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415783 | ||||||
| chr8:27415831
|
T | C | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-4064T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415831 | ||||||
| chr8:27415866
|
C | T | 100 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(97): Show | 101 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.205-4029C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415866 | ||||||
| chr8:27415896
|
TAGAG | T | 7 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0175others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-3995_205-3992d others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27415896 | |||||
| chr8:27415933
|
A | G | 2 | a0002c0006t0001g0006a0002c0006t0001g0010 | 2 | HG00738.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.205-3962A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415933 | ||||||
| chr8:27416112
|
C | A | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.205-3783C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416112 | ||||||
| chr8:27416113
|
A | C | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.205-3782A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416113 | ||||||
| chr8:27416135
|
A | C | 1 | a0002c0006t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.205-3760A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416135 | ||||||
| chr8:27416150
|
G | T | 117 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(114): Show | 120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.205-3745G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416150 | ||||||
| chr8:27416323
|
A | G | 16 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(13): Show | 18 | HG00738.hp1 HG02486.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.205-3572A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416323 | ||||||
| chr8:27416394
|
C | T | 22 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(19): Show | 23 | HG00408.hp1 HG00639.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.205-3501C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416394 | ||||||
| chr8:27416525
|
CTG | C | 113 | a0001c0002t0001g0296a0001c0007t0003g0277a0001c0007t0003g0278others(110): Show | 115 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.205-3367_205-3366d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27416525 | |||||
| chr8:27416527
|
G | A | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-3368G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416527 | ||||||
| chr8:27416650
|
A | G | 1 | a0001c0009t0002g0310 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.205-3245A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416650 | ||||||
| chr8:27416662
|
A | G | 1 | a0002c0003t0002g0259 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.205-3233A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416662 | ||||||
| chr8:27416723
|
C | T | 6 | a0002c0003t0002g0012a0002c0004t0002g0001a0002c0004t0002g0011others(3): Show | 8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-3172C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416723 | ||||||
| chr8:27416726
|
T | C | 1 | a0002c0006t0001g0038 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.205-3169T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416726 | ||||||
| chr8:27416728
|
A | G | 1 | a0002c0003t0002g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.205-3167A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416728 | ||||||
| chr8:27416914
|
G | A | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-2981G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416914 | ||||||
| chr8:27417080
|
C | T | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-2815C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417080 | ||||||
| chr8:27417114
|
G | T | 232 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(229): Show | 237 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.205-2781G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417114 | ||||||
| chr8:27417206
|
C | T | 1 | a0002c0006t0001g0323 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.205-2689C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417206 | ||||||
| chr8:27417207
|
A | G | 232 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(229): Show | 237 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.205-2688A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417207 | ||||||
| chr8:27417258
|
G | A | 229 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(226): Show | 234 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.205-2637G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417258 | ||||||
| chr8:27417281
|
G | A | 1 | a0001c0007t0003g0137 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.205-2614G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417281 | ||||||
| chr8:27417396
|
G | C | 8 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-2499G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417396 | ||||||
| chr8:27417414
|
T | C | 100 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(97): Show | 101 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.205-2481T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417414 | ||||||
| chr8:27417441
|
G | A | 2 | a0001c0001t0003g0015a0001c0001t0003g0016 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.205-2454G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417441 | ||||||
| chr8:27417447
|
A | AGG | 15 | a0002c0003t0002g0004a0002c0003t0002g0067a0002c0003t0002g0239others(12): Show | 16 | HG00408.hp2 HG00733.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.205-2446_205-2445d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27417447 | |||||
| chr8:27417558
|
T | A | 229 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(226): Show | 234 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.205-2337T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417558 | ||||||
| chr8:27417777
|
A | G | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.205-2118A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417777 | ||||||
| chr8:27417835
|
G | A | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-2060G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417835 | ||||||
| chr8:27417954
|
G | A | 4 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-1941G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417954 | ||||||
| chr8:27417968
|
G | A | 8 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-1927G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417968 | ||||||
| chr8:27417992
|
A | G | 239 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(236): Show | 244 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.205-1903A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417992 | ||||||
| chr8:27418001
|
G | A | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-1894G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418001 | ||||||
| chr8:27418132
|
T | G | 100 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(97): Show | 101 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.205-1763T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418132 | ||||||
| chr8:27418209
|
G | T | 113 | a0001c0002t0001g0296a0001c0007t0003g0277a0001c0007t0003g0278others(110): Show | 115 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.205-1686G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418209 | ||||||
| chr8:27418251
|
A | C | 1 | a0001c0001t0003g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.205-1644A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418251 | ||||||
| chr8:27418277
|
T | C | 107 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(104): Show | 109 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.205-1618T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418277 | ||||||
| chr8:27418283
|
C | T | 8 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-1612C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418283 | ||||||
| chr8:27418387
|
T | C | 114 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(111): Show | 116 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.205-1508T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418387 | ||||||
| chr8:27418466
|
A | T | 8 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-1429A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418466 | ||||||
| chr8:27418594
|
C | T | 244 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(241): Show | 249 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.205-1301C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418594 | ||||||
| chr8:27418692
|
T | C | 107 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(104): Show | 109 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.205-1203T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418692 | ||||||
| chr8:27418751
|
G | T | 6 | a0001c0007t0003g0277a0001c0007t0003g0278a0001c0007t0003g0279others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-1144G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418751 | ||||||
| chr8:27418772
|
A | C | 107 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(104): Show | 109 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.205-1123A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418772 | ||||||
| chr8:27419009
|
C | A | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-886C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419009 | ||||||
| chr8:27419030
|
GA | G | 100 | a0001c0008t0003g0114a0001c0009t0002g0103a0001c0009t0002g0106others(97): Show | 102 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.205-855delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27419030 | |||||
| chr8:27419099
|
G | A | 6 | a0002c0003t0002g0012a0002c0004t0002g0001a0002c0004t0002g0011others(3): Show | 8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-796G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419099 | ||||||
| chr8:27419100
|
C | T | 100 | a0001c0008t0003g0114a0001c0009t0002g0103a0001c0009t0002g0106others(97): Show | 102 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.205-795C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419100 | ||||||
| chr8:27419124
|
A | G | 6 | a0001c0007t0003g0277a0001c0007t0003g0278a0001c0007t0003g0279others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-771A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419124 | ||||||
| chr8:27419188
|
G | A | 6 | a0002c0003t0002g0003a0002c0003t0002g0261a0002c0003t0002g0262others(3): Show | 7 | HG00099.hp2 HG00741.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.205-707G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419188 | ||||||
| chr8:27419252
|
T | C | 229 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(226): Show | 234 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.205-643T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419252 | ||||||
| chr8:27419487
|
T | C | 6 | a0001c0001t0003g0022a0001c0001t0003g0294a0001c0013t0003g0301others(3): Show | 6 | HG00639.hp1 HG00733.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-408T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419487 | ||||||
| chr8:27419638
|
T | C | 5 | a0001c0002t0001g0079a0001c0002t0001g0157a0001c0002t0001g0161others(2): Show | 5 | HG01928.hp2 NA18978.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-257T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419638 | ||||||
| chr8:27420111
|
G | A | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.383+38G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420111 | ||||||
| chr8:27420125
|
G | A | 6 | a0001c0007t0003g0277a0001c0007t0003g0278a0001c0007t0003g0279others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+52G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420125 | ||||||
| chr8:27420161
|
C | A | 2 | a0002c0003t0002g0003a0002c0003t0002g0263 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.383+88C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420161 | ||||||
| chr8:27420422
|
G | A | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.384-235G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420422 | ||||||
| chr8:27420514
|
G | A | 1 | a0001c0001t0003g0034 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.384-143G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420514 | ||||||
| chr8:27420549
|
C | A | 1 | a0001c0002t0001g0170 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.384-108C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420549 | ||||||
| chr8:27420641
|
G | A | 1 | a0001c0001t0003g0073 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.384-16G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420641 | ||||||
| chr8:27420785
|
C | T | 2 | a0002c0004t0002g0208a0002c0004t0002g0210 | 2 | NA18962.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.471+41C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27420785 | ||||||
| chr8:27420790
|
C | T | 1 | a0002c0006t0001g0323 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.471+46C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27420790 | ||||||
| chr8:27420904
|
G | A | 7 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0183others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+160G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27420904 | ||||||
| chr8:27421029
|
A | G | 1 | a0001c0002t0001g0158 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.471+285A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421029 | ||||||
| chr8:27421278
|
C | CTATT | 9 | a0001c0002t0001g0080a0001c0002t0001g0118a0001c0002t0001g0138others(6): Show | 9 | HG00673.hp2 HG02040.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.471+580_471+583dup others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr8 | 27421278 | |||||
| chr8:27421278
|
CTATT | C | 130 | a0001c0001t0003g0185a0001c0002t0001g0005a0001c0002t0001g0076others(127): Show | 134 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.471+580_471+583del others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr8 | 27421278 | |||||
| chr8:27421278
|
CTATTTAT others(1): Show |
C | 35 | a0001c0001t0003g0022a0001c0001t0003g0088a0001c0001t0003g0113others(32): Show | 35 | HG00639.hp1 HG00733.hp1 HG02258.hp2 others(32): Show |
intron_variant | MODIFIER | c.471+576_471+583del others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr8 | 27421278 | |||||
| chr8:27421278
|
CTATTTAT others(5): Show |
C | 2 | a0001c0007t0003g0277a0001c0007t0003g0278 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.471+572_471+583del others(12): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr8 | 27421278 | |||||
| chr8:27421278
|
CTATTTAT others(9): Show |
C | 1 | a0001c0011t0001g0142 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.471+568_471+583del others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr8 | 27421278 | |||||
| chr8:27421278
|
CTATTTAT others(17): Show |
C | 77 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(74): Show | 78 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.471+560_471+583del others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr8 | 27421278 | |||||
| chr8:27421330
|
A | G | 118 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(115): Show | 120 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.471+586A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421330 | ||||||
| chr8:27421334
|
G | T | 1 | a0001c0001t0003g0318 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.471+590G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421334 | ||||||
| chr8:27421340
|
T | G | 7 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+596T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421340 | ||||||
| chr8:27421467
|
C | T | 1 | a0001c0001t0003g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.471+723C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421467 | ||||||
| chr8:27421517
|
A | C | 1 | a0001c0001t0003g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.471+773A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421517 | ||||||
| chr8:27421546
|
A | C | 6 | a0002c0003t0002g0012a0002c0004t0002g0001a0002c0004t0002g0011others(3): Show | 8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.472-758A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421546 | ||||||
| chr8:27421587
|
A | G | 8 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.472-717A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421587 | ||||||
| chr8:27421590
|
A | G | 8 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.472-714A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421590 | ||||||
| chr8:27421682
|
C | A | 17 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(14): Show | 19 | HG00738.hp1 HG02486.hp1 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.472-622C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421682 | ||||||
| chr8:27421706
|
T | C | 240 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(237): Show | 245 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.472-598T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421706 | ||||||
| chr8:27421857
|
G | A | 1 | a0001c0002t0001g0188 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.472-447G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421857 | ||||||
| chr8:27421883
|
A | C | 240 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(237): Show | 245 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.472-421A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421883 | ||||||
| chr8:27422039
|
C | T | 2 | a0001c0011t0001g0142a0001c0011t0001g0165 | 2 | NA18949.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.472-265C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27422039 | ||||||
| chr8:27422142
|
C | A | 1 | a0002c0003t0004g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.472-162C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27422142 | ||||||
| chr8:27422188
|
G | A | 237 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(234): Show | 242 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.472-116G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27422188 | ||||||
| chr8:27422200
|
G | C | 1 | a0001c0002t0001g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.472-104G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27422200 | ||||||
| chr8:27422600
|
C | G | 99 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(96): Show | 100 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.551+217C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27422600 | ||||||
| chr8:27422885
|
C | T | 3 | a0002c0003t0002g0223a0002c0003t0002g0311a0002c0006t0002g0317 | 3 | NA18961.hp1 NA18969.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.551+502C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27422885 | ||||||
| chr8:27422923
|
G | A | 5 | a0001c0002t0001g0077a0001c0002t0001g0119a0001c0002t0001g0120others(2): Show | 5 | NA18945.hp2 NA18957.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.551+540G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27422923 | ||||||
| chr8:27422955
|
G | A | 5 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0276others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.551+572G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27422955 | ||||||
| chr8:27423279
|
C | G | 1 | a0004c0015t0001g0193 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.551+896C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423279 | ||||||
| chr8:27423296
|
C | T | 1 | a0001c0001t0003g0025 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.551+913C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423296 | ||||||
| chr8:27423343
|
C | T | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.551+960C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423343 | ||||||
| chr8:27423426
|
C | T | 1 | a0001c0009t0002g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551+1043C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423426 | ||||||
| chr8:27423427
|
G | A | 1 | a0002c0004t0002g0298 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.551+1044G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423427 | ||||||
| chr8:27423479
|
A | C | 1 | a0002c0006t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.551+1096A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423479 | ||||||
| chr8:27423519
|
G | A | 3 | a0001c0013t0003g0301a0001c0013t0003g0302a0001c0013t0003g0304 | 3 | HG00639.hp1 HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.551+1136G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423519 | ||||||
| chr8:27423595
|
G | T | 1 | a0001c0001t0003g0276 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.551+1212G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423595 | ||||||
| chr8:27423616
|
G | A | 1 | a0002c0003t0002g0267 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.551+1233G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423616 | ||||||
| chr8:27423665
|
T | C | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.551+1282T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423665 | ||||||
| chr8:27423719
|
C | T | 3 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0205 | 3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.551+1336C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423719 | ||||||
| chr8:27423750
|
G | A | 2 | a0001c0001t0003g0059a0001c0001t0005g0060 | 2 | HG01069.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.551+1367G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423750 | ||||||
| chr8:27423920
|
G | C | 1 | a0002c0006t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.551+1537G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423920 | ||||||
| chr8:27424323
|
G | A | 1 | a0001c0002t0001g0167 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.551+1940G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27424323 | ||||||
| chr8:27424379
|
T | C | 40 | a0001c0008t0003g0114a0001c0009t0002g0106a0001c0012t0004g0053others(37): Show | 41 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.551+1996T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27424379 | ||||||
| chr8:27424395
|
G | A | 64 | a0001c0009t0002g0103a0001c0012t0004g0030a0001c0012t0004g0211others(61): Show | 65 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.551+2012G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27424395 | ||||||
| chr8:27424546
|
C | T | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.551+2163C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27424546 | ||||||
| chr8:27424692
|
C | T | 1 | a0002c0003t0002g0266 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.551+2309C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27424692 | ||||||
| chr8:27424871
|
GA | G | 227 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(224): Show | 232 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.551+2499delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr8 | 27424871 | |||||
| chr8:27424880
|
A | T | 1 | a0002c0004t0002g0210 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.551+2497A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27424880 | ||||||
| chr8:27425084
|
TTA | T | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.551+2703_551+2704d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr8 | 27425084 | |||||
| chr8:27425101
|
A | G | 3 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0052 | 3 | HG02080.hp1 NA18978.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.551+2718A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425101 | ||||||
| chr8:27425254
|
T | G | 39 | a0001c0008t0003g0114a0001c0009t0002g0106a0001c0012t0004g0053others(36): Show | 40 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.551+2871T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425254 | ||||||
| chr8:27425520
|
C | G | 64 | a0001c0009t0002g0103a0001c0012t0004g0030a0001c0012t0004g0211others(61): Show | 65 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.551+3137C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425520 | ||||||
| chr8:27425675
|
A | G | 100 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(97): Show | 101 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.551+3292A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425675 | ||||||
| chr8:27425744
|
C | T | 8 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.551+3361C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425744 | ||||||
| chr8:27425961
|
G | T | 1 | a0001c0002t0001g0152 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.551+3578G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425961 | ||||||
| chr8:27425987
|
T | C | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.551+3604T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425987 | ||||||
| chr8:27426071
|
C | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.551+3688C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426071 | ||||||
| chr8:27426107
|
G | A | 1 | a0001c0009t0002g0313 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.551+3724G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426107 | ||||||
| chr8:27426121
|
G | A | 1 | a0002c0003t0002g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.551+3738G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426121 | ||||||
| chr8:27426156
|
C | T | 4 | a0001c0009t0002g0106a0002c0003t0002g0270a0002c0003t0002g0274others(1): Show | 4 | HG00423.hp2 HG02080.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.551+3773C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426156 | ||||||
| chr8:27426209
|
A | G | 1 | a0010c0032t0003g0284 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.551+3826A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426209 | ||||||
| chr8:27426507
|
A | G | 3 | a0001c0008t0003g0314a0001c0008t0003g0315a0001c0008t0003g0316 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.552-3586A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426507 | ||||||
| chr8:27426537
|
A | G | 3 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0322 | 3 | HG02055.hp2 HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.552-3556A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426537 | ||||||
| chr8:27426558
|
CAGACATT others(22): Show |
C | 6 | a0002c0003t0002g0012a0002c0004t0002g0001a0002c0004t0002g0011others(3): Show | 8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.552-3504_552-3476d others(31): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr8 | 27426558 | |||||
| chr8:27426582
|
G | T | 1 | a0001c0010t0003g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.552-3511G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426582 | ||||||
| chr8:27426855
|
T | C | 1 | a0001c0001t0003g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.552-3238T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426855 | ||||||
| chr8:27426857
|
A | G | 1 | a0002c0006t0001g0038 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.552-3236A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426857 | ||||||
| chr8:27426877
|
G | A | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.552-3216G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426877 | ||||||
| chr8:27426907
|
T | G | 1 | a0001c0007t0003g0135 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.552-3186T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426907 | ||||||
| chr8:27426994
|
A | G | 5 | a0001c0007t0003g0277a0001c0007t0003g0278a0001c0007t0003g0279others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.552-3099A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426994 | ||||||
| chr8:27427005
|
G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.552-3088G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427005 | ||||||
| chr8:27427070
|
C | T | 3 | a0001c0007t0003g0279a0001c0007t0003g0280a0001c0007t0003g0281 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.552-3023C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427070 | ||||||
| chr8:27427139
|
T | A | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.552-2954T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427139 | ||||||
| chr8:27427140
|
C | A | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.552-2953C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427140 | ||||||
| chr8:27427141
|
T | C | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.552-2952T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427141 | ||||||
| chr8:27427175
|
C | T | 113 | a0001c0002t0001g0296a0001c0007t0003g0277a0001c0007t0003g0278others(110): Show | 115 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.552-2918C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427175 | ||||||
| chr8:27427254
|
A | G | 1 | a0004c0015t0001g0193 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.552-2839A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427254 | ||||||
| chr8:27427506
|
C | G | 6 | a0002c0003t0002g0012a0002c0004t0002g0001a0002c0004t0002g0011others(3): Show | 8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.552-2587C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427506 | ||||||
| chr8:27427659
|
A | C | 1 | a0002c0006t0001g0126 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.552-2434A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427659 | ||||||
| chr8:27427661
|
G | A | 3 | a0002c0003t0002g0004a0002c0003t0002g0067a0002c0006t0001g0092 | 4 | HG01257.hp1 HG01258.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.552-2432G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427661 | ||||||
| chr8:27427787
|
G | C | 7 | a0001c0002t0001g0296a0001c0008t0003g0243a0001c0008t0003g0295others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.552-2306G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427787 | ||||||
| chr8:27428016
|
A | G | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.552-2077A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428016 | ||||||
| chr8:27428196
|
G | T | 1 | a0002c0004t0002g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.552-1897G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428196 | ||||||
| chr8:27428208
|
G | C | 5 | a0001c0007t0003g0277a0001c0007t0003g0278a0001c0007t0003g0279others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.552-1885G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428208 | ||||||
| chr8:27428444
|
C | T | 6 | a0002c0003t0002g0012a0002c0004t0002g0001a0002c0004t0002g0011others(3): Show | 8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.552-1649C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428444 | ||||||
| chr8:27428463
|
G | T | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.552-1630G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428463 | ||||||
| chr8:27428591
|
T | C | 1 | a0002c0003t0002g0055 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.552-1502T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428591 | ||||||
| chr8:27428737
|
G | T | 1 | a0001c0002t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.552-1356G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428737 | ||||||
| chr8:27428862
|
G | A | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.552-1231G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428862 | ||||||
| chr8:27429094
|
A | G | 116 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(113): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.552-999A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429094 | ||||||
| chr8:27429127
|
A | G | 4 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.552-966A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429127 | ||||||
| chr8:27429331
|
C | T | 3 | a0001c0002t0001g0145a0001c0002t0001g0169a0001c0002t0001g0306 | 3 | NA19003.hp2 NA19005.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.552-762C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429331 | ||||||
| chr8:27429554
|
A | C | 1 | a0001c0001t0003g0022 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.552-539A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429554 | ||||||
| chr8:27429615
|
A | T | 8 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.552-478A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429615 | ||||||
| chr8:27429621
|
T | C | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.552-472T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429621 | ||||||
| chr8:27429722
|
A | T | 2 | a0001c0001t0003g0015a0001c0001t0003g0016 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.552-371A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429722 | ||||||
| chr8:27429810
|
C | T | 74 | a0001c0002t0001g0296a0001c0008t0003g0114a0001c0008t0003g0243others(71): Show | 76 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.552-283C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429810 | ||||||
| chr8:27430275
|
A | G | 1 | a0001c0001t0003g0054 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.615-89A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 6/30 | chr8 | 27430275 | ||||||
| chr8:27430359
|
T | C | 1 | a0001c0011t0001g0148 | 1 | HG02056.hp2 | splice_region_variant&intron_variant | LOW | c.615-5T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 6/30 | chr8 | 27430359 | ||||||
| chr8:27430480
|
T | A | 42 | a0001c0008t0003g0114a0001c0008t0003g0292a0001c0008t0003g0319others(39): Show | 43 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.669+62T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430480 | ||||||
| chr8:27430516
|
T | C | 118 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(115): Show | 119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.669+98T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430516 | ||||||
| chr8:27430548
|
A | G | 2 | a0002c0006t0001g0006a0002c0006t0001g0282 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.669+130A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430548 | ||||||
| chr8:27430612
|
C | T | 2 | a0001c0001t0003g0186a0001c0001t0003g0187 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.669+194C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430612 | ||||||
| chr8:27430748
|
G | A | 1 | a0002c0004t0002g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.670-128G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430748 | ||||||
| chr8:27430784
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.670-92G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430784 | ||||||
| chr8:27430797
|
T | C | 38 | a0002c0003t0002g0004a0002c0003t0002g0012a0002c0003t0002g0055others(35): Show | 39 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.670-79T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430797 | ||||||
| chr8:27431294
|
C | G | 1 | a0001c0001t0003g0318 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.811-104C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 8/30 | chr8 | 27431294 | ||||||
| chr8:27431484
|
C | T | 2 | a0002c0006t0001g0006a0002c0006t0001g0282 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.885+12C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27431484 | ||||||
| chr8:27431523
|
C | T | 4 | a0001c0002t0001g0080a0001c0002t0001g0149a0001c0002t0001g0152others(1): Show | 4 | NA18945.hp1 NA18980.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.885+51C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27431523 | ||||||
| chr8:27431609
|
G | A | 109 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(106): Show | 110 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.885+137G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27431609 | ||||||
| chr8:27431804
|
T | C | 72 | a0001c0008t0003g0114a0002c0003t0002g0003a0002c0003t0002g0023others(69): Show | 75 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.885+332T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27431804 | ||||||
| chr8:27431892
|
G | C | 38 | a0002c0003t0002g0004a0002c0003t0002g0012a0002c0003t0002g0055others(35): Show | 39 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.886-368G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27431892 | ||||||
| chr8:27431895
|
G | C | 38 | a0002c0003t0002g0004a0002c0003t0002g0012a0002c0003t0002g0055others(35): Show | 39 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.886-365G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27431895 | ||||||
| chr8:27431994
|
A | AT | 113 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(110): Show | 114 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.886-255dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr8 | 27431994 | |||||
| chr8:27431994
|
A | ATT | 6 | a0001c0008t0003g0243a0001c0008t0003g0295a0001c0008t0003g0314others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.886-256_886-255dup others(2): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr8 | 27431994 | |||||
| chr8:27432064
|
A | G | 5 | a0001c0008t0003g0243a0001c0008t0003g0295a0001c0008t0003g0314others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.886-196A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27432064 | ||||||
| chr8:27432095
|
C | T | 113 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(110): Show | 114 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.886-165C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27432095 | ||||||
| chr8:27432256
|
A | G | 2 | a0002c0004t0002g0244a0002c0004t0002g0245 | 2 | HG01168.hp1 HG01169.hp2 |
splice_region_variant&intron_variant | LOW | c.886-4A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27432256 | ||||||
| chr8:27432418
|
T | C | 113 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(110): Show | 114 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.987+57T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27432418 | ||||||
| chr8:27432446
|
T | C | 113 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(110): Show | 114 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.987+85T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27432446 | ||||||
| chr8:27432581
|
G | A | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.987+220G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27432581 | ||||||
| chr8:27432680
|
C | T | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.987+319C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27432680 | ||||||
| chr8:27432767
|
G | GCAGAGCG others(2): Show |
113 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(110): Show | 114 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.987+408_987+409ins others(9): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | INFO_REALIGN_3_PRIME | chr8 | 27432767 | |||||
| chr8:27432980
|
C | T | 1 | a0002c0006t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.988-455C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27432980 | ||||||
| chr8:27433011
|
G | A | 110 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(107): Show | 111 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.988-424G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27433011 | ||||||
| chr8:27433040
|
T | C | 2 | a0002c0006t0001g0006a0002c0006t0001g0282 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.988-395T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27433040 | ||||||
| chr8:27433154
|
T | G | 1 | a0001c0009t0002g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.988-281T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27433154 | ||||||
| chr8:27433216
|
G | A | 1 | a0001c0002t0001g0175 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.988-219G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27433216 | ||||||
| chr8:27433264
|
G | A | 1 | a0002c0026t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.988-171G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27433264 | ||||||
| chr8:27433277
|
C | CA | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.988-157dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | INFO_REALIGN_3_PRIME | chr8 | 27433277 | |||||
| chr8:27433987
|
G | T | 1 | a0001c0002t0001g0133 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1106-106G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 11/30 | chr8 | 27433987 | ||||||
| chr8:27434040
|
T | C | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1106-53T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 11/30 | chr8 | 27434040 | ||||||
| chr8:27434232
|
C | T | 78 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(75): Show | 78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1145+100C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 12/30 | chr8 | 27434232 | ||||||
| chr8:27434367
|
C | A | 1 | a0002c0006t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1146-146C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 12/30 | chr8 | 27434367 | ||||||
| chr8:27434603
|
G | A | 2 | a0002c0003t0002g0236a0002c0003t0002g0256 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1192+44G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/30 | chr8 | 27434603 | ||||||
| chr8:27434770
|
A | G | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1192+211A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/30 | chr8 | 27434770 | ||||||
| chr8:27434775
|
A | G | 113 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(110): Show | 114 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1192+216A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/30 | chr8 | 27434775 | ||||||
| chr8:27434989
|
A | T | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1192+430A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/30 | chr8 | 27434989 | ||||||
| chr8:27435220
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1193-523C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/30 | chr8 | 27435220 | ||||||
| chr8:27435639
|
C | G | 2 | a0002c0006t0001g0006a0002c0006t0001g0282 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1193-104C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/30 | chr8 | 27435639 | ||||||
| chr8:27435804
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1243+11G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 14/30 | chr8 | 27435804 | ||||||
| chr8:27435818
|
G | T | 65 | a0001c0008t0003g0114a0002c0003t0002g0003a0002c0003t0002g0023others(62): Show | 68 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1243+25G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 14/30 | chr8 | 27435818 | ||||||
| chr8:27436212
|
G | A | 1 | a0001c0001t0005g0060 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1244-39G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 14/30 | chr8 | 27436212 | ||||||
| chr8:27436364
|
T | G | 1 | a0001c0025t0001g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1341+16T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436364 | ||||||
| chr8:27436448
|
A | C | 1 | a0002c0006t0001g0126 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1341+100A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436448 | ||||||
| chr8:27436472
|
G | A | 103 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(100): Show | 103 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1341+124G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436472 | ||||||
| chr8:27436609
|
T | C | 3 | a0002c0005t0001g0026a0002c0005t0001g0031a0002c0005t0001g0033 | 3 | HG01928.hp1 HG01943.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1341+261T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436609 | ||||||
| chr8:27436631
|
C | T | 9 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(6): Show | 9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1341+283C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436631 | ||||||
| chr8:27436667
|
A | G | 1 | a0002c0003t0002g0258 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1341+319A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436667 | ||||||
| chr8:27436745
|
GAAGA | G | 5 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1342-368_1342-365d others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr8 | 27436745 | |||||
| chr8:27436780
|
A | G | 5 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1342-342A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436780 | ||||||
| chr8:27436989
|
G | A | 1 | a0002c0005t0001g0033 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1342-133G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436989 | ||||||
| chr8:27437015
|
C | G | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1342-107C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27437015 | ||||||
| chr8:27437089
|
G | C | 90 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(87): Show | 90 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1342-33G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27437089 | ||||||
| chr8:27437250
|
C | T | 1 | a0002c0003t0002g0241 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1426+44C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 16/30 | chr8 | 27437250 | ||||||
| chr8:27437306
|
T | C | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1427-90T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 16/30 | chr8 | 27437306 | ||||||
| chr8:27437592
|
A | G | 243 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(240): Show | 248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.1527+96A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 17/30 | chr8 | 27437592 | ||||||
| chr8:27438096
|
T | A | 7 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0183others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1643+216T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438096 | ||||||
| chr8:27438281
|
G | C | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1643+401G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438281 | ||||||
| chr8:27438462
|
C | CTGATTCT others(538): Show |
1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1644-566_1644-565i others(547): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | |||||
| chr8:27438462
|
C | CTGATTCT others(535): Show |
2 | a0002c0006t0001g0006a0002c0006t0001g0282 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1644-566_1644-565i others(544): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | |||||
| chr8:27438462
|
C | CTGATTCT others(531): Show |
4 | a0001c0007t0003g0277a0001c0007t0003g0278a0001c0007t0003g0280others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1644-566_1644-565i others(540): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | |||||
| chr8:27438462
|
C | CTGATTCT others(536): Show |
1 | a0002c0004t0002g0011 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1644-566_1644-565i others(545): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | |||||
| chr8:27438462
|
C | CTGATTCT others(535): Show |
161 | a0001c0001t0003g0022a0001c0001t0003g0088a0001c0001t0003g0093others(158): Show | 165 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.1644-566_1644-565i others(544): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | |||||
| chr8:27438462
|
C | CTGATTCT others(535): Show |
83 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(80): Show | 84 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1644-566_1644-565i others(544): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | |||||
| chr8:27438462
|
C | CTGATTCT others(539): Show |
2 | a0001c0010t0003g0231a0002c0003t0002g0311 | 2 | HG02486.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1644-566_1644-565i others(548): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | |||||
| chr8:27438474
|
G | A | 3 | a0002c0003t0002g0270a0002c0003t0002g0274a0002c0006t0001g0126 | 3 | HG02080.hp2 NA18943.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1644-557G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438474 | ||||||
| chr8:27438487
|
A | G | 128 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(125): Show | 129 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1644-544A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438487 | ||||||
| chr8:27438516
|
C | T | 1 | a0004c0015t0001g0200 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1644-515C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438516 | ||||||
| chr8:27438573
|
G | A | 17 | a0002c0003t0002g0223a0002c0005t0001g0002a0002c0005t0001g0083others(14): Show | 18 | HG00408.hp1 HG00639.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1644-458G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438573 | ||||||
| chr8:27438639
|
C | T | 7 | a0001c0008t0003g0243a0001c0008t0003g0295a0001c0008t0003g0314others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1644-392C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438639 | ||||||
| chr8:27438682
|
C | T | 2 | a0002c0006t0001g0006a0002c0006t0001g0282 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1644-349C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438682 | ||||||
| chr8:27438952
|
ATCTG | A | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1644-72_1644-69del others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438952 | |||||
| chr8:27438965
|
T | C | 1 | a0002c0005t0001g0201 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1644-66T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438965 | ||||||
| chr8:27439147
|
A | G | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1744+16A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 19/30 | chr8 | 27439147 | ||||||
| chr8:27439498
|
C | T | 7 | a0001c0008t0003g0243a0001c0008t0003g0295a0001c0008t0003g0314others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1834+100C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439498 | ||||||
| chr8:27439523
|
T | G | 7 | a0001c0008t0003g0243a0001c0008t0003g0295a0001c0008t0003g0314others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1834+125T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439523 | ||||||
| chr8:27439629
|
A | G | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1834+231A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439629 | ||||||
| chr8:27439685
|
T | C | 90 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(87): Show | 90 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1834+287T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439685 | ||||||
| chr8:27439710
|
G | T | 1 | a0002c0003t0002g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1834+312G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439710 | ||||||
| chr8:27439821
|
C | T | 9 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(6): Show | 9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1835-416C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439821 | ||||||
| chr8:27439838
|
C | T | 5 | a0001c0002t0001g0077a0001c0002t0001g0119a0001c0002t0001g0120others(2): Show | 5 | NA18945.hp2 NA18957.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1835-399C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439838 | ||||||
| chr8:27440058
|
G | A | 8 | a0001c0001t0003g0022a0001c0001t0003g0093a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1835-179G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440058 | ||||||
| chr8:27440077
|
G | A | 104 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(101): Show | 104 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1835-160G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440077 | ||||||
| chr8:27440108
|
G | C | 67 | a0001c0008t0003g0114a0002c0003t0002g0003a0002c0003t0002g0023others(64): Show | 70 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1835-129G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440108 | ||||||
| chr8:27440164
|
A | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-73A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440164 | ||||||
| chr8:27440165
|
A | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-72A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440165 | ||||||
| chr8:27440169
|
C | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-68C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440169 | ||||||
| chr8:27440173
|
G | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-64G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440173 | ||||||
| chr8:27440174
|
G | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-63G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440174 | ||||||
| chr8:27440178
|
T | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-59T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440178 | ||||||
| chr8:27440179
|
T | C | 243 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(240): Show | 248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.1835-58T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440179 | ||||||
| chr8:27440182
|
G | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-55G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440182 | ||||||
| chr8:27440183
|
G | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-54G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440183 | ||||||
| chr8:27440185
|
T | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-52T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440185 | ||||||
| chr8:27440186
|
G | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-51G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440186 | ||||||
| chr8:27440187
|
G | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-50G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440187 | ||||||
| chr8:27440188
|
G | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-49G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440188 | ||||||
| chr8:27440190
|
G | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-47G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440190 | ||||||
| chr8:27440192
|
G | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-45G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440192 | ||||||
| chr8:27440194
|
C | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-43C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440194 | ||||||
| chr8:27440197
|
G | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-40G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440197 | ||||||
| chr8:27440199
|
C | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-38C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440199 | ||||||
| chr8:27440200
|
T | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-37T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440200 | ||||||
| chr8:27440201
|
C | G | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-36C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440201 | ||||||
| chr8:27440202
|
C | G | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-35C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440202 | ||||||
| chr8:27440205
|
C | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-32C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440205 | ||||||
| chr8:27440206
|
A | C | 1 | a0001c0001t0003g0029 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1835-31A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440206 | ||||||
| chr8:27440209
|
C | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-28C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440209 | ||||||
| chr8:27440212
|
G | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-25G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440212 | ||||||
| chr8:27440214
|
C | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-23C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440214 | ||||||
| chr8:27440215
|
C | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-22C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440215 | ||||||
| chr8:27440216
|
T | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-21T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440216 | ||||||
| chr8:27440228
|
A | G | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1835-9A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440228 | ||||||
| chr8:27440229
|
C | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | splice_region_variant&intron_variant | LOW | c.1835-8C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440229 | ||||||
| chr8:27440231
|
C | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | splice_region_variant&intron_variant | LOW | c.1835-6C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440231 | ||||||
| chr8:27440462
|
G | T | 3 | a0002c0006t0001g0234a0002c0006t0001g0290a0002c0006t0001g0291 | 3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2039+21G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440462 | ||||||
| chr8:27440526
|
C | T | 1 | a0001c0002t0001g0192 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2039+85C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440526 | ||||||
| chr8:27440544
|
G | A | 1 | a0001c0002t0001g0188 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2039+103G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440544 | ||||||
| chr8:27440561
|
A | G | 244 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(241): Show | 249 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.2039+120A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440561 | ||||||
| chr8:27440862
|
C | G | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2039+421C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440862 | ||||||
| chr8:27440863
|
C | T | 16 | a0001c0001t0003g0022a0001c0001t0003g0088a0001c0001t0003g0093others(13): Show | 16 | HG00639.hp1 HG00733.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2039+422C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440863 | ||||||
| chr8:27440892
|
G | A | 8 | a0001c0001t0003g0025a0001c0001t0003g0050a0001c0001t0003g0081others(5): Show | 8 | HG00738.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.2039+451G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440892 | ||||||
| chr8:27440914
|
C | T | 1 | a0001c0001t0003g0059 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2039+473C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440914 | ||||||
| chr8:27441039
|
G | A | 1 | a0001c0002t0001g0005 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2039+598G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441039 | ||||||
| chr8:27441159
|
T | C | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2039+718T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441159 | ||||||
| chr8:27441207
|
C | T | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2039+766C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441207 | ||||||
| chr8:27441402
|
T | A | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2039+961T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441402 | ||||||
| chr8:27441444
|
A | G | 9 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(6): Show | 9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2039+1003A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441444 | ||||||
| chr8:27441570
|
C | A | 107 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(104): Show | 108 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.2039+1129C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441570 | ||||||
| chr8:27441760
|
A | G | 39 | a0002c0003t0002g0004a0002c0003t0002g0012a0002c0003t0002g0055others(36): Show | 40 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.2040-1115A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441760 | ||||||
| chr8:27441810
|
G | C | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2040-1065G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441810 | ||||||
| chr8:27441894
|
A | T | 119 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(116): Show | 120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2040-981A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441894 | ||||||
| chr8:27441952
|
A | G | 119 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(116): Show | 120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2040-923A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441952 | ||||||
| chr8:27441994
|
T | G | 1 | a0002c0003t0002g0259 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2040-881T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441994 | ||||||
| chr8:27442036
|
C | T | 119 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(116): Show | 120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2040-839C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442036 | ||||||
| chr8:27442054
|
G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2040-821G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442054 | ||||||
| chr8:27442136
|
G | C | 73 | a0001c0008t0003g0114a0002c0003t0002g0003a0002c0003t0002g0023others(70): Show | 76 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.2040-739G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442136 | ||||||
| chr8:27442146
|
A | G | 1 | a0001c0001t0003g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2040-729A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442146 | ||||||
| chr8:27442220
|
A | G | 8 | a0001c0001t0003g0088a0001c0001t0003g0093a0001c0001t0003g0294others(5): Show | 8 | HG00639.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040-655A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442220 | ||||||
| chr8:27442223
|
T | C | 234 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(231): Show | 239 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.2040-652T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442223 | ||||||
| chr8:27442269
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2040-606A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442269 | ||||||
| chr8:27442418
|
A | G | 119 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(116): Show | 120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2040-457A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442418 | ||||||
| chr8:27442452
|
GGATGTTT others(14): Show |
G | 7 | a0001c0001t0003g0178a0001c0001t0003g0227a0001c0001t0003g0228others(4): Show | 7 | HG02572.hp2 HG02818.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2040-417_2040-397d others(23): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr8 | 27442452 | |||||
| chr8:27442507
|
C | A | 1 | a0002c0003t0002g0254 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2040-368C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442507 | ||||||
| chr8:27442525
|
A | G | 8 | a0001c0002t0001g0144a0001c0002t0001g0155a0001c0002t0001g0159others(5): Show | 8 | HG00423.hp2 HG00544.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040-350A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442525 | ||||||
| chr8:27442571
|
T | C | 94 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(91): Show | 95 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.2040-304T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442571 | ||||||
| chr8:27442581
|
G | T | 1 | a0002c0003t0002g0267 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2040-294G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442581 | ||||||
| chr8:27442604
|
A | G | 119 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(116): Show | 120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2040-271A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442604 | ||||||
| chr8:27442642
|
C | T | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2040-233C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442642 | ||||||
| chr8:27442653
|
C | A | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2040-222C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442653 | ||||||
| chr8:27443104
|
C | A | 119 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(116): Show | 120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2148+121C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443104 | ||||||
| chr8:27443297
|
T | A | 2 | a0002c0006t0001g0006a0002c0006t0001g0282 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2148+314T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443297 | ||||||
| chr8:27443331
|
A | G | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2148+348A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443331 | ||||||
| chr8:27443643
|
A | G | 119 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(116): Show | 120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2149-563A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443643 | ||||||
| chr8:27443681
|
C | G | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2149-525C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443681 | ||||||
| chr8:27443934
|
G | A | 47 | a0001c0008t0003g0243a0001c0008t0003g0295a0001c0008t0003g0314others(44): Show | 48 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.2149-272G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443934 | ||||||
| chr8:27443974
|
A | G | 119 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(116): Show | 120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2149-232A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443974 | ||||||
| chr8:27444292
|
C | T | 2 | a0002c0006t0001g0006a0002c0006t0001g0282 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2214+21C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444292 | ||||||
| chr8:27444359
|
G | T | 1 | a0002c0006t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2214+88G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444359 | ||||||
| chr8:27444838
|
C | T | 1 | a0002c0018t0002g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2214+567C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444838 | ||||||
| chr8:27444886
|
C | G | 1 | a0002c0004t0002g0248 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2214+615C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444886 | ||||||
| chr8:27444915
|
T | C | 241 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(238): Show | 246 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.2214+644T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444915 | ||||||
| chr8:27444916
|
G | A | 112 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(109): Show | 113 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2214+645G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444916 | ||||||
| chr8:27444932
|
A | G | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2214+661A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444932 | ||||||
| chr8:27445004
|
C | A | 1 | a0002c0003t0002g0257 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2214+733C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445004 | ||||||
| chr8:27445006
|
T | G | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2214+735T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445006 | ||||||
| chr8:27445131
|
A | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2215-663A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445131 | ||||||
| chr8:27445214
|
T | G | 243 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(240): Show | 248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.2215-580T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445214 | ||||||
| chr8:27445237
|
A | C | 1 | a0001c0002t0001g0214 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2215-557A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445237 | ||||||
| chr8:27445327
|
T | C | 243 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(240): Show | 248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.2215-467T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445327 | ||||||
| chr8:27445367
|
C | T | 5 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2215-427C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445367 | ||||||
| chr8:27445368
|
A | G | 117 | a0001c0008t0003g0114a0002c0003t0002g0003a0002c0003t0002g0004others(114): Show | 121 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2215-426A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445368 | ||||||
| chr8:27445489
|
A | C | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2215-305A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445489 | ||||||
| chr8:27445498
|
T | C | 112 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(109): Show | 113 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2215-296T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445498 | ||||||
| chr8:27445563
|
T | C | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2215-231T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445563 | ||||||
| chr8:27445609
|
A | G | 243 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(240): Show | 248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.2215-185A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445609 | ||||||
| chr8:27445683
|
C | T | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2215-111C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445683 | ||||||
| chr8:27445951
|
G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2340+32G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27445951 | ||||||
| chr8:27445962
|
G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2340+43G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27445962 | ||||||
| chr8:27446044
|
C | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2340+125C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446044 | ||||||
| chr8:27446224
|
T | A | 2 | a0001c0002t0001g0149a0001c0002t0001g0152 | 2 | NA18980.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2340+305T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446224 | ||||||
| chr8:27446263
|
A | T | 2 | a0002c0006t0001g0006a0002c0006t0001g0282 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2340+344A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446263 | ||||||
| chr8:27446483
|
G | T | 2 | a0002c0005t0001g0083a0002c0005t0001g0085 | 2 | NA18979.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2340+564G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446483 | ||||||
| chr8:27446506
|
G | A | 1 | a0001c0008t0003g0314 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2340+587G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446506 | ||||||
| chr8:27446564
|
T | C | 19 | a0001c0002t0001g0079a0001c0002t0001g0118a0001c0002t0001g0140others(16): Show | 19 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.2340+645T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446564 | ||||||
| chr8:27446662
|
A | G | 1 | a0001c0001t0003g0071 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2340+743A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446662 | ||||||
| chr8:27446753
|
G | A | 1 | a0002c0003t0002g0247 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2340+834G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446753 | ||||||
| chr8:27446872
|
A | G | 5 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2340+953A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446872 | ||||||
| chr8:27446923
|
T | C | 1 | a0002c0004t0002g0209 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2340+1004T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446923 | ||||||
| chr8:27447148
|
C | T | 1 | a0001c0002t0001g0192 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2340+1229C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27447148 | ||||||
| chr8:27447237
|
A | C | 1 | a0001c0001t0003g0228 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2340+1318A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27447237 | ||||||
| chr8:27447438
|
C | T | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2340+1519C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27447438 | ||||||
| chr8:27447640
|
C | T | 2 | a0001c0008t0003g0319a0001c0008t0003g0320 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2340+1721C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27447640 | ||||||
| chr8:27448024
|
G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2340+2105G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448024 | ||||||
| chr8:27448088
|
A | G | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2340+2169A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448088 | ||||||
| chr8:27448246
|
T | C | 1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2340+2327T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448246 | ||||||
| chr8:27448409
|
C | T | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2341-2340C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448409 | ||||||
| chr8:27448427
|
A | G | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2341-2322A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448427 | ||||||
| chr8:27448559
|
A | G | 1 | a0001c0008t0003g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2341-2190A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448559 | ||||||
| chr8:27448586
|
C | T | 107 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(104): Show | 107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.2341-2163C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448586 | ||||||
| chr8:27448597
|
AACTTACA others(3): Show |
A | 109 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(106): Show | 109 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.2341-2137_2341-212 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr8 | 27448597 | |||||
| chr8:27448642
|
G | A | 127 | a0001c0008t0003g0114a0002c0003t0002g0003a0002c0003t0002g0004others(124): Show | 132 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.2341-2107G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448642 | ||||||
| chr8:27448771
|
C | T | 2 | a0002c0004t0002g0244a0002c0004t0002g0245 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2341-1978C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448771 | ||||||
| chr8:27449033
|
G | A | 1 | a0002c0003t0002g0260 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2341-1716G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449033 | ||||||
| chr8:27449034
|
T | A | 70 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(67): Show | 70 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.2341-1715T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449034 | ||||||
| chr8:27449083
|
C | T | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2341-1666C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449083 | ||||||
| chr8:27449106
|
C | T | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2341-1643C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449106 | ||||||
| chr8:27449145
|
G | A | 2 | a0002c0006t0001g0006a0002c0006t0001g0282 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2341-1604G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449145 | ||||||
| chr8:27449307
|
A | G | 1 | a0001c0001t0003g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2341-1442A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449307 | ||||||
| chr8:27449403
|
T | C | 2 | a0002c0006t0001g0010a0002c0017t0002g0252 | 2 | HG00738.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2341-1346T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449403 | ||||||
| chr8:27449509
|
G | T | 12 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320others(9): Show | 12 | HG02486.hp1 HG02647.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2341-1240G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449509 | ||||||
| chr8:27449555
|
G | A | 65 | a0001c0008t0003g0114a0002c0003t0002g0003a0002c0003t0002g0023others(62): Show | 68 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.2341-1194G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449555 | ||||||
| chr8:27449578
|
A | G | 62 | a0002c0003t0002g0004a0002c0003t0002g0012a0002c0003t0002g0055others(59): Show | 64 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2341-1171A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449578 | ||||||
| chr8:27449663
|
C | T | 12 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320others(9): Show | 12 | HG02486.hp1 HG02647.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2341-1086C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449663 | ||||||
| chr8:27449718
|
G | C | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2341-1031G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449718 | ||||||
| chr8:27449758
|
G | C | 92 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(89): Show | 92 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.2341-991G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449758 | ||||||
| chr8:27449819
|
A | G | 55 | a0002c0003t0002g0004a0002c0003t0002g0012a0002c0003t0002g0055others(52): Show | 57 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.2341-930A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449819 | ||||||
| chr8:27450005
|
A | G | 91 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(88): Show | 91 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.2341-744A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450005 | ||||||
| chr8:27450200
|
C | A | 12 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320others(9): Show | 12 | HG02486.hp1 HG02647.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2341-549C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450200 | ||||||
| chr8:27450276
|
T | C | 1 | a0002c0003t0004g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2341-473T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450276 | ||||||
| chr8:27450394
|
C | T | 9 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(6): Show | 9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2341-355C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450394 | ||||||
| chr8:27450487
|
G | A | 133 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0012others(130): Show | 138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.2341-262G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450487 | ||||||
| chr8:27450507
|
C | A | 1 | a0001c0010t0003g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2341-242C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450507 | ||||||
| chr8:27450508
|
G | A | 25 | a0002c0004t0002g0001a0002c0004t0002g0011a0002c0004t0002g0013others(22): Show | 27 | HG00438.hp2 HG00621.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.2341-241G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450508 | ||||||
| chr8:27451021
|
G | A | 96 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(93): Show | 96 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.2488-22G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 25/30 | chr8 | 27451021 | ||||||
| chr8:27451169
|
C | G | 4 | a0001c0001t0003g0025a0001c0001t0003g0091a0003c0014t0003g0043others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2523+91C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451169 | ||||||
| chr8:27451173
|
G | A | 5 | a0001c0008t0003g0243a0001c0008t0003g0295a0001c0008t0003g0314others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2523+95G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451173 | ||||||
| chr8:27451202
|
C | T | 1 | a0002c0006t0001g0323 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2523+124C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451202 | ||||||
| chr8:27451255
|
C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2523+177C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451255 | ||||||
| chr8:27451273
|
G | A | 2 | a0002c0006t0001g0234a0002c0006t0001g0290 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2523+195G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451273 | ||||||
| chr8:27451332
|
A | G | 235 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(232): Show | 240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2524-153A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451332 | ||||||
| chr8:27451364
|
C | G | 9 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(6): Show | 9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2524-121C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451364 | ||||||
| chr8:27451365
|
G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2524-120G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451365 | ||||||
| chr8:27451444
|
C | T | 64 | a0002c0003t0002g0003a0002c0003t0002g0023a0002c0003t0002g0056others(61): Show | 67 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.2524-41C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451444 | ||||||
| chr8:27451581
|
G | A | 1 | a0001c0001t0003g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2548+72G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451581 | ||||||
| chr8:27451600
|
G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2548+91G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451600 | ||||||
| chr8:27451731
|
G | A | 1 | a0001c0010t0003g0297 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2548+222G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451731 | ||||||
| chr8:27451749
|
C | T | 1 | a0001c0002t0001g0138 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2548+240C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451749 | ||||||
| chr8:27451760
|
A | G | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2548+251A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451760 | ||||||
| chr8:27451822
|
T | C | 109 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(106): Show | 109 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.2548+313T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451822 | ||||||
| chr8:27451862
|
T | C | 241 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(238): Show | 246 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.2548+353T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451862 | ||||||
| chr8:27451927
|
T | A | 5 | a0001c0008t0003g0243a0001c0008t0003g0295a0001c0008t0003g0314others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2548+418T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451927 | ||||||
| chr8:27452103
|
T | G | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2548+594T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452103 | ||||||
| chr8:27452140
|
T | C | 55 | a0002c0003t0002g0004a0002c0003t0002g0012a0002c0003t0002g0055others(52): Show | 57 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.2548+631T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452140 | ||||||
| chr8:27452469
|
G | A | 2 | a0001c0001t0003g0015a0001c0001t0003g0016 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2549-645G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452469 | ||||||
| chr8:27452559
|
C | CA | 223 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(220): Show | 228 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.2549-537dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | INFO_REALIGN_3_PRIME | chr8 | 27452559 | |||||
| chr8:27452559
|
C | CAA | 12 | a0001c0001t0003g0184a0001c0001t0003g0227a0001c0001t0003g0305others(9): Show | 12 | HG00733.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2549-538_2549-537d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | INFO_REALIGN_3_PRIME | chr8 | 27452559 | |||||
| chr8:27452632
|
G | A | 2 | a0001c0001t0003g0021a0001c0001t0003g0048 | 2 | NA18956.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2549-482G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452632 | ||||||
| chr8:27452651
|
C | T | 1 | a0001c0002t0001g0147 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2549-463C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452651 | ||||||
| chr8:27452653
|
A | G | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2549-461A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452653 | ||||||
| chr8:27452705
|
A | G | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2549-409A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452705 | ||||||
| chr8:27452744
|
G | A | 1 | a0001c0002t0001g0169 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2549-370G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452744 | ||||||
| chr8:27452892
|
G | C | 1 | a0002c0003t0002g0269 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2549-222G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452892 | ||||||
| chr8:27452973
|
G | A | 9 | a0001c0010t0003g0229a0001c0010t0003g0230a0001c0010t0003g0231others(6): Show | 9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2549-141G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452973 | ||||||
| chr8:27452991
|
G | A | 1 | a0001c0013t0003g0304 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2549-123G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452991 | ||||||
| chr8:27453029
|
A | G | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.2549-85A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27453029 | ||||||
| chr8:27453200
|
G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2595+40G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453200 | ||||||
| chr8:27453291
|
C | T | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2595+131C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453291 | ||||||
| chr8:27453389
|
C | G | 1 | a0001c0001t0003g0045 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2595+229C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453389 | ||||||
| chr8:27453502
|
T | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2595+342T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453502 | ||||||
| chr8:27453600
|
C | T | 2 | a0002c0003t0002g0262a0002c0003t0002g0275 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2595+440C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453600 | ||||||
| chr8:27453608
|
C | T | 17 | a0002c0003t0002g0004a0002c0003t0002g0012a0002c0003t0002g0067others(14): Show | 18 | HG00408.hp2 HG00609.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2595+448C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453608 | ||||||
| chr8:27453727
|
T | A | 34 | a0002c0003t0002g0004a0002c0003t0002g0012a0002c0003t0002g0055others(31): Show | 35 | HG00408.hp2 HG00609.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2596-427T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453727 | ||||||
| chr8:27453728
|
A | T | 1 | a0002c0006t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2596-426A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453728 | ||||||
| chr8:27453814
|
T | C | 243 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(240): Show | 248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.2596-340T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453814 | ||||||
| chr8:27453859
|
A | G | 243 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(240): Show | 248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.2596-295A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453859 | ||||||
| chr8:27454104
|
C | T | 3 | a0001c0008t0003g0292a0001c0008t0003g0319a0001c0008t0003g0320 | 3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2596-50C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27454104 | ||||||
| chr8:27454523
|
C | T | 109 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(106): Show | 109 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
splice_region_variant&intron_variant | LOW | c.2734-8C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 29/30 | chr8 | 27454523 | ||||||
| chr8:27454527
|
C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | splice_region_variant&intron_variant | LOW | c.2734-4C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 29/30 | chr8 | 27454527 | ||||||
| chr8:27454618
|
G | A | 109 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(106): Show | 109 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
splice_region_variant&intron_variant | LOW | c.2814+7G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27454618 | ||||||
| chr8:27454715
|
C | T | 1 | a0002c0005t0001g0002 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.2814+104C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27454715 | ||||||
| chr8:27454790
|
G | A | 25 | a0001c0002t0001g0005a0001c0002t0001g0077a0001c0002t0001g0116others(22): Show | 25 | HG00423.hp1 HG01496.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.2814+179G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27454790 | ||||||
| chr8:27454812
|
G | A | 2 | a0002c0003t0002g0270a0002c0003t0002g0274 | 2 | HG02080.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2814+201G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27454812 | ||||||
| chr8:27454909
|
A | G | 234 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(231): Show | 239 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.2814+298A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27454909 | ||||||
| chr8:27454947
|
ATG | A | 65 | a0002c0003t0002g0003a0002c0003t0002g0023a0002c0003t0002g0056others(62): Show | 68 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.2814+340_2814+341d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27454947 | |||||
| chr8:27455150
|
CTT | C | 4 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2814+541_2814+542d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27455150 | |||||
| chr8:27455170
|
T | A | 97 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(94): Show | 97 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2814+559T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455170 | ||||||
| chr8:27455292
|
G | A | 125 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0012others(122): Show | 130 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.2814+681G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455292 | ||||||
| chr8:27455375
|
T | A | 1 | a0002c0005t0001g0002 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.2814+764T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455375 | ||||||
| chr8:27455431
|
C | T | 5 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2814+820C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455431 | ||||||
| chr8:27455568
|
G | T | 109 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(106): Show | 109 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.2814+957G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455568 | ||||||
| chr8:27455637
|
C | G | 4 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2814+1026C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455637 | ||||||
| chr8:27455838
|
C | A | 4 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0032others(1): Show | 4 | HG01109.hp2 HG01255.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.2814+1227C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455838 | ||||||
| chr8:27455872
|
G | A | 1 | a0010c0032t0003g0284 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2814+1261G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455872 | ||||||
| chr8:27456122
|
T | G | 1 | a0002c0003t0002g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2814+1511T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456122 | ||||||
| chr8:27456251
|
C | T | 3 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0205 | 3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2814+1640C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456251 | ||||||
| chr8:27456297
|
C | T | 4 | a0001c0001t0003g0088a0001c0001t0003g0113a0001c0001t0003g0115others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2814+1686C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456297 | ||||||
| chr8:27456332
|
T | G | 1 | a0001c0002t0001g0155 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2814+1721T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456332 | ||||||
| chr8:27456338
|
C | T | 4 | a0001c0001t0003g0025a0001c0001t0003g0091a0003c0014t0003g0043others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2814+1727C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456338 | ||||||
| chr8:27456371
|
G | A | 4 | a0001c0002t0001g0127a0001c0002t0001g0128a0001c0002t0001g0192others(1): Show | 4 | NA19000.hp1 NA19057.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.2814+1760G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456371 | ||||||
| chr8:27456371
|
G | T | 239 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(236): Show | 244 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.2814+1760G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456371 | ||||||
| chr8:27456391
|
G | A | 1 | a0001c0002t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2814+1780G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456391 | ||||||
| chr8:27457052
|
A | G | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2815-1242A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457052 | ||||||
| chr8:27457302
|
A | G | 241 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(238): Show | 246 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.2815-992A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457302 | ||||||
| chr8:27457578
|
T | C | 7 | a0001c0001t0003g0178a0001c0001t0003g0227a0001c0001t0003g0228others(4): Show | 7 | HG02572.hp2 HG02818.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2815-716T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457578 | ||||||
| chr8:27457841
|
T | G | 241 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(238): Show | 246 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.2815-453T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457841 | ||||||
| chr8:27457906
|
C | T | 1 | a0001c0002t0001g0080 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2815-388C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457906 | ||||||
| chr8:27457925
|
A | C | 1 | a0001c0001t0003g0184 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2815-369A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457925 | ||||||
| chr8:27457930
|
G | A | 241 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(238): Show | 246 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.2815-364G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457930 | ||||||
| chr8:27457971
|
G | T | 2 | a0002c0003t0002g0255a0002c0003t0006g0044 | 2 | NA18960.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2815-323G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457971 | ||||||
| chr8:27457975
|
CA | C | 6 | a0001c0002t0001g0176a0001c0002t0001g0235a0001c0002t0001g0296others(3): Show | 6 | HG03041.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2815-296delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27457975 | |||||
| chr8:27457975
|
CAAAAAAA | C | 118 | a0002c0003t0002g0003a0002c0003t0002g0004a0002c0003t0002g0012others(115): Show | 123 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.2815-302_2815-296d others(9): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27457975 | |||||
| chr8:27457975
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0157 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2815-305_2815-296d others(12): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27457975 | |||||
| chr8:27457996
|
AAAG | A | 20 | a0001c0001t0003g0024a0001c0001t0003g0035a0001c0001t0003g0036others(17): Show | 20 | HG00323.hp2 HG01070.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2815-296_2815-294d others(5): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27457996 | |||||
| chr8:27457997
|
AAG | A | 81 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0021others(78): Show | 81 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.2815-295_2815-294d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27457997 | |||||
| chr8:27457998
|
AG | A | 9 | a0001c0001t0003g0017a0001c0001t0003g0037a0001c0001t0003g0047others(6): Show | 9 | HG00438.hp1 HG01109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2815-295delG | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457998 | ||||||
| chr8:27458140
|
G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2815-154G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27458140 | ||||||
| chr8:27458173
|
T | A | 1 | a0001c0001t0003g0027 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2815-121T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27458173 | ||||||
| chr8:27458209
|
T | C | 236 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(233): Show | 241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.2815-85T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27458209 |