Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5053 |
|---|---|
| ensemblid | ENSG00000171759.10 |
| hgncid | 8582 |
| symbol | PAH |
| name | phenylalanine hydroxylase |
| refseq_nuc | NM_000277.3 |
| refseq_prot | NP_000268.1 |
| ensembl_nuc | ENST00000553106.6 |
| ensembl_prot | ENSP00000448059.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 102836889 |
| end | 102917244 |
| strand | - |
| ver | v1.2 |
| region | chr12:102836889-102917244 |
| region5000 | chr12:102831889-102922244 |
| regionname0 | PAH_chr12_102836889_102917244 |
| regionname5000 | PAH_chr12_102831889_102922244 |
| 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 | 0/0 | 452 | 300 | 95 | 72 | 89 | 12 | 32 | 66 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0002 | 0/0 | 452 | 9 | 0 | 0 | 9 | 0 | 0 | 8 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0003 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0004 | 0/0 | 452 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0005 | 0/0 | 452 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| 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 | 1359 | 139 | 57 | 45 | 12 | 6 | 19 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0002 | 0/0 | 1359 | 76 | 1 | 12 | 54 | 2 | 7 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0003 | 0/0 | 1359 | 42 | 2 | 9 | 23 | 3 | 5 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0004 | 0/0 | 1359 | 14 | 12 | 2 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0005 | 0/0 | 1359 | 9 | 0 | 0 | 9 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0006 | 0/0 | 1359 | 6 | 5 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0007 | 0/0 | 1359 | 6 | 6 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0008 | 0/0 | 1359 | 6 | 5 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0009 | 0/0 | 1359 | 5 | 5 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0010 | 0/0 | 1359 | 2 | 0 | 2 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0011 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0012 | 0/0 | 1359 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0013 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0014 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0015 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0016 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| c0017 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2401 | 150 | 31 | 31 | 67 | 6 | 15 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0002 | 0/0 | 2401 | 60 | 23 | 26 | 0 | 2 | 9 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0003 | 0/0 | 2401 | 47 | 2 | 11 | 25 | 3 | 6 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0004 | 0/0 | 2401 | 10 | 9 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0005 | 0/0 | 2401 | 5 | 5 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0006 | 0/0 | 2397 | 4 | 4 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0007 | 0/0 | 2401 | 4 | 4 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0008 | 0/0 | 2401 | 4 | 4 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0009 | 0/0 | 2401 | 4 | 2 | 2 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0010 | 0/0 | 2401 | 3 | 3 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0011 | 0/0 | 2402 | 3 | 1 | 1 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0012 | 0/0 | 2401 | 2 | 2 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0013 | 0/0 | 2401 | 2 | 2 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0014 | 0/0 | 2402 | 2 | 0 | 1 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0015 | 0/0 | 2401 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0016 | 0/0 | 2401 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0017 | 0/0 | 2402 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0018 | 0/0 | 2401 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0019 | 0/0 | 2401 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0020 | 0/0 | 2401 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0021 | 0/0 | 2401 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0022 | 0/0 | 2401 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0023 | 0/0 | 2401 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0024 | 0/0 | 2402 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0025 | 0/0 | 2401 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| t0026 | 0/0 | 2401 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0003 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| 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 | 1359 | 139 | 57 | 45 | 12 | 6 | 19 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0002 | 0/0 | 1359 | 76 | 1 | 12 | 54 | 2 | 7 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0003 | 0/0 | 1359 | 42 | 2 | 9 | 23 | 3 | 5 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0004 | 0/0 | 1359 | 14 | 12 | 2 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0006 | 0/0 | 1359 | 6 | 5 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0007 | 0/0 | 1359 | 6 | 6 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0008 | 0/0 | 1359 | 6 | 5 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0009 | 0/0 | 1359 | 5 | 5 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0010 | 0/0 | 1359 | 2 | 0 | 2 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0011 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0012 | 0/0 | 1359 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0014 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0015 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0002c0005 | 0/0 | 1359 | 9 | 0 | 0 | 9 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0003c0013 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0004c0016 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0005c0017 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3759 | 61 | 20 | 17 | 12 | 4 | 8 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0001t0002 | 0/0 | 3759 | 53 | 18 | 25 | 0 | 1 | 9 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0001t0003 | 0/0 | 3759 | 3 | 0 | 1 | 0 | 0 | 2 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0001t0004 | 0/0 | 3759 | 7 | 6 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0001t0006 | 0/0 | 3755 | 4 | 4 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0001t0007 | 0/0 | 3759 | 3 | 3 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0001t0009 | 0/0 | 3759 | 4 | 2 | 2 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0001t0011 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0001t0012 | 0/0 | 3759 | 2 | 2 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0001t0025 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0002t0001 | 0/0 | 3759 | 68 | 1 | 10 | 49 | 2 | 6 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0002t0003 | 0/0 | 3759 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0002t0011 | 0/0 | 3760 | 2 | 0 | 1 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0002t0015 | 0/0 | 3759 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0002t0019 | 0/0 | 3759 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0002t0020 | 0/0 | 3759 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0002t0021 | 0/0 | 3759 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0002t0022 | 0/0 | 3759 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0003t0001 | 0/0 | 3759 | 7 | 0 | 0 | 6 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0003t0003 | 0/0 | 3759 | 32 | 1 | 8 | 16 | 3 | 4 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0003t0005 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0003t0014 | 0/0 | 3760 | 2 | 0 | 1 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0004t0001 | 0/0 | 3759 | 7 | 6 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0004t0002 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0004t0007 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0004t0008 | 0/0 | 3759 | 4 | 4 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0004t0026 | 0/0 | 3759 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0006t0001 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0006t0002 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0006t0004 | 0/0 | 3759 | 3 | 3 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0006t0016 | 0/0 | 3759 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0007t0002 | 0/0 | 3759 | 2 | 2 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0007t0010 | 0/0 | 3759 | 3 | 3 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0007t0017 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0008t0001 | 0/0 | 3759 | 3 | 3 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0008t0018 | 0/0 | 3759 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0008t0023 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0008t0024 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0009t0005 | 0/0 | 3759 | 3 | 3 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0009t0013 | 0/0 | 3759 | 2 | 2 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0010t0001 | 0/0 | 3759 | 2 | 0 | 2 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0011t0002 | 0/0 | 3759 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0012t0002 | 0/0 | 3759 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0014t0003 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0001c0015t0002 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0002c0005t0003 | 0/0 | 3759 | 9 | 0 | 0 | 9 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0003c0013t0005 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0004c0016t0003 | 0/0 | 3759 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| a0005c0017t0001 | 0/0 | 3759 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | copy fasta | chr12 | 102831889 | 102922244 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0009g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0009g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0009g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0009g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0012g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0001t0025g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0003 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0011g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0011g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0015g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0019g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0020g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0021g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0002t0022g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0014g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0003t0014g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0008g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0008g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0004t0026g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0006t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0006t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0006t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0006t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0006t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0006t0016g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0007t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0007t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0007t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0007t0010g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0007t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0007t0017g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0008t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0008t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0008t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0008t0018g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0008t0023g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0008t0024g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0009t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0009t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0009t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0009t0013g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0009t0013g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0010t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0011t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0012t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0014t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0001c0015t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0002c0005t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0002c0005t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0002c0005t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0002c0005t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0002c0005t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0002c0005t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0002c0005t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0002c0005t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0002c0005t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0003c0013t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0004c0016t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| a0005c0017t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0003 | g0267 | EUR | GBR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0057 | EUR | GBR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0262 | EUR | FIN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00323 | hp2 | a0001 | c0012 | t0002 | g0214 | EUR | FIN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | CHS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00408 | hp2 | a0001 | c0003 | t0003 | g0287 | EAS | CHS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | CHS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | CHS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00597 | hp2 | a0001 | c0003 | t0003 | g0244 | EAS | CHS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00609 | hp1 | a0001 | c0003 | t0003 | g0289 | EAS | CHS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | CHS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00639 | hp1 | a0001 | c0001 | t0009 | g0305 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00673 | hp1 | a0001 | c0003 | t0003 | g0288 | EAS | CHS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | CHS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00735 | hp1 | a0001 | c0003 | t0003 | g0257 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00735 | hp2 | a0001 | c0003 | t0003 | g0259 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG00741 | hp2 | a0001 | c0001 | t0009 | g0306 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01081 | hp1 | a0001 | c0011 | t0002 | g0069 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01081 | hp2 | a0001 | c0003 | t0003 | g0270 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01109 | hp1 | a0005 | c0017 | t0001 | g0142 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01167 | hp1 | a0001 | c0010 | t0001 | g0001 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01168 | hp2 | a0001 | c0003 | t0003 | g0264 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01169 | hp1 | a0001 | c0010 | t0001 | g0001 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01175 | hp1 | a0001 | c0002 | t0011 | g0030 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01175 | hp2 | a0001 | c0004 | t0026 | g0304 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01192 | hp2 | a0001 | c0003 | t0003 | g0272 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0147 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0081 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01256 | hp1 | a0001 | c0002 | t0003 | g0231 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0108 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01257 | hp2 | a0001 | c0003 | t0003 | g0263 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01258 | hp2 | a0001 | c0003 | t0014 | g0279 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01496 | hp1 | a0001 | c0008 | t0018 | g0215 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | CLM | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0151 | EUR | IBS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0079 | EUR | IBS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01516 | hp2 | a0001 | c0003 | t0003 | g0266 | EUR | IBS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01517 | hp2 | a0001 | c0003 | t0003 | g0274 | EUR | IBS | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01884 | hp2 | a0001 | c0008 | t0023 | g0242 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01891 | hp1 | a0001 | c0001 | t0025 | g0234 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01943 | hp2 | a0001 | c0003 | t0003 | g0268 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02040 | hp1 | a0001 | c0003 | t0003 | g0243 | EAS | KHV | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | KHV | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02055 | hp1 | a0001 | c0001 | t0011 | g0132 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0121 | EAS | KHV | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | KHV | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02132 | hp2 | a0001 | c0002 | t0020 | g0078 | EAS | KHV | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | CDX | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02155 | hp2 | a0001 | c0003 | t0003 | g0282 | EAS | CDX | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | CDX | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02165 | hp2 | a0001 | c0003 | t0003 | g0284 | EAS | CDX | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02257 | hp1 | a0003 | c0013 | t0005 | g0237 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0146 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0295 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02280 | hp2 | a0001 | c0007 | t0010 | g0031 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02293 | hp1 | a0004 | c0016 | t0003 | g0281 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02300 | hp1 | a0001 | c0003 | t0003 | g0280 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02451 | hp1 | a0001 | c0004 | t0008 | g0303 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02451 | hp2 | a0001 | c0007 | t0002 | g0178 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02523 | hp1 | a0001 | c0003 | t0003 | g0245 | EAS | KHV | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0115 | EAS | KHV | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02572 | hp2 | a0001 | c0003 | t0003 | g0291 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0190 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02630 | hp1 | a0001 | c0008 | t0001 | g0228 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02630 | hp2 | a0001 | c0004 | t0007 | g0145 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0227 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0255 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02723 | hp1 | a0001 | c0006 | t0002 | g0211 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0158 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0149 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02818 | hp2 | a0001 | c0015 | t0002 | g0148 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02886 | hp1 | a0001 | c0008 | t0001 | g0133 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02886 | hp2 | a0001 | c0009 | t0005 | g0236 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02895 | hp1 | a0001 | c0006 | t0004 | g0293 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02895 | hp2 | a0001 | c0007 | t0010 | g0033 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0285 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02896 | hp2 | a0001 | c0006 | t0004 | g0297 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02897 | hp1 | a0001 | c0006 | t0004 | g0292 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0286 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02970 | hp2 | a0001 | c0007 | t0017 | g0043 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03041 | hp1 | a0001 | c0008 | t0001 | g0134 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0299 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | MSL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03130 | hp1 | a0001 | c0004 | t0008 | g0302 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03139 | hp1 | a0001 | c0009 | t0005 | g0235 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0298 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | MSL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0226 | AFR | MSL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0103 | AFR | MSL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0107 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03491 | hp1 | a0001 | c0003 | t0003 | g0006 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03492 | hp2 | a0001 | c0003 | t0003 | g0006 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03516 | hp1 | a0001 | c0008 | t0024 | g0241 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0141 | AFR | ESN | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03540 | hp2 | a0001 | c0007 | t0010 | g0032 | AFR | GWD | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0294 | AFR | MSL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03579 | hp2 | a0001 | c0009 | t0005 | g0238 | AFR | MSL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0095 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03710 | hp2 | a0001 | c0002 | t0021 | g0083 | SAS | PJL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0119 | SAS | BEB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | BEB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0271 | SAS | BEB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0153 | SAS | STU | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG04199 | hp2 | a0001 | c0003 | t0003 | g0256 | SAS | STU | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG04204 | hp2 | a0001 | c0003 | t0003 | g0276 | SAS | STU | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG04228 | hp1 | a0001 | c0006 | t0016 | g0163 | SAS | STU | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | YRI | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18522 | hp2 | a0001 | c0004 | t0008 | g0301 | AFR | YRI | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18747 | hp1 | a0002 | c0005 | t0003 | g0246 | EAS | CHB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | CHB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18939 | hp2 | a0002 | c0005 | t0003 | g0251 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18944 | hp2 | a0001 | c0002 | t0019 | g0035 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18954 | hp1 | a0002 | c0005 | t0003 | g0249 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18960 | hp2 | a0001 | c0003 | t0003 | g0275 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18968 | hp1 | a0001 | c0003 | t0003 | g0265 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18968 | hp2 | a0001 | c0002 | t0022 | g0025 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18970 | hp1 | a0002 | c0005 | t0003 | g0253 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18982 | hp1 | a0001 | c0003 | t0003 | g0290 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18983 | hp2 | a0002 | c0005 | t0003 | g0250 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18985 | hp1 | a0001 | c0003 | t0003 | g0269 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18985 | hp2 | a0001 | c0002 | t0011 | g0089 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0144 | AFR | LWK | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19043 | hp1 | a0001 | c0014 | t0003 | g0261 | AFR | LWK | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19043 | hp2 | a0001 | c0006 | t0001 | g0213 | AFR | LWK | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19054 | hp2 | a0001 | c0003 | t0014 | g0278 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19065 | hp2 | a0001 | c0003 | t0003 | g0277 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19066 | hp2 | a0002 | c0005 | t0003 | g0252 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19067 | hp2 | a0001 | c0002 | t0015 | g0007 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19068 | hp2 | a0002 | c0005 | t0003 | g0247 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0049 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19076 | hp1 | a0002 | c0005 | t0003 | g0248 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19077 | hp2 | a0001 | c0003 | t0003 | g0258 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19086 | hp1 | a0001 | c0003 | t0003 | g0273 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19089 | hp2 | a0002 | c0005 | t0003 | g0254 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19090 | hp1 | a0001 | c0003 | t0003 | g0283 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0229 | AFR | YRI | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0140 | AFR | YRI | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | ASW | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ASW | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | GIH | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0114 | SAS | GIH | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02109 | hp1 | a0001 | c0009 | t0013 | g0240 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02109 | hp2 | a0001 | c0007 | t0002 | g0040 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02486 | hp1 | a0001 | c0009 | t0013 | g0239 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02486 | hp2 | a0001 | c0004 | t0008 | g0300 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG02559 | hp2 | a0001 | c0003 | t0005 | g0260 | AFR | ACB | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0143 | AFR | MSL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0230 | AFR | MSL | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0296 | AFR | USA | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA20300 | hp1 | a0001 | c0004 | t0002 | g0150 | AFR | USA | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | USA | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | PAH_chr12_102831889_102922244 | PAH | chr12 | 102831889 | 102922244 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:102846927
|
C | A | 1 | a0004 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.937G>T | p.Ala313Ser | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/13 | 1051/3759 | 937/1359 | 313/452 | chr12 | 102846927 | ||
| chr12:102852837
|
T | C | 1 | a0003 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.820A>G | p.Lys274Glu | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/13 | 934/3759 | 820/1359 | 274/452 | chr12 | 102852837 | ||
| chr12:102866605
|
T | C | 1 | a0005 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.500A>G | p.Asn167Ser | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/13 | 614/3759 | 500/1359 | 167/452 | chr12 | 102866605 | ||
| chr12:102912801
|
C | T | 1 | a0002 | 9 | NA18747.hp1 NA18939.hp2 NA18954.hp1 others(6): Show |
missense_variant | MODERATE | c.158G>A | p.Arg53His | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/13 | 272/3759 | 158/1359 | 53/452 | chr12 | 102912801 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:102840437
|
A | G | 4 | a0001c0004a0001c0007a0001c0015others(1): Show | 22 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(19): Show |
synonymous_variant | LOW | c.1278T>C | p.Asn426Asn | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/13 | 1392/3759 | 1278/1359 | 426/452 | chr12 | 102840437 | ||
| chr12:102840473
|
G | A | 1 | a0001c0012 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.1242C>T | p.Tyr414Tyr | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/13 | 1356/3759 | 1242/1359 | 414/452 | chr12 | 102840473 | ||
| chr12:102843690
|
G | C | 11 | a0001c0001a0001c0002a0001c0007others(8): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
synonymous_variant | LOW | c.1155C>G | p.Leu385Leu | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/13 | 1269/3759 | 1155/1359 | 385/452 | chr12 | 102843690 | ||
| chr12:102846901
|
G | A | 2 | a0001c0009a0003c0013 | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.963C>T | p.Leu321Leu | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/13 | 1077/3759 | 963/1359 | 321/452 | chr12 | 102846901 | ||
| chr12:102852885
|
G | A | 1 | a0001c0014 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.772C>T | p.Leu258Leu | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/13 | 886/3759 | 772/1359 | 258/452 | chr12 | 102852885 | ||
| chr12:102852922
|
C | T | 2 | a0001c0002a0001c0010 | 78 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(75): Show |
synonymous_variant | LOW | c.735G>A | p.Val245Val | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/13 | 849/3759 | 735/1359 | 245/452 | chr12 | 102852922 | ||
| chr12:102855146
|
C | T | 8 | a0001c0001a0001c0006a0001c0007others(5): Show | 160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
synonymous_variant | LOW | c.696G>A | p.Gln232Gln | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/13 | 810/3759 | 696/1359 | 232/452 | chr12 | 102855146 | ||
| chr12:102855161
|
C | T | 1 | a0001c0011 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.681G>A | p.Leu227Leu | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/13 | 795/3759 | 681/1359 | 227/452 | chr12 | 102855161 | ||
| chr12:102855233
|
G | A | 1 | a0001c0010 | 2 | HG01167.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.609C>T | p.Cys203Cys | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/13 | 723/3759 | 609/1359 | 203/452 | chr12 | 102855233 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:102837205
|
A | C | 6 | a0001c0001t0007a0001c0003t0005a0001c0004t0007others(3): Show | 13 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1970T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 1970 | chr12 | 102837205 | |||||
| chr12:102837358
|
A | G | 1 | a0001c0001t0012 | 2 | HG02257.hp2 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1817T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 1817 | chr12 | 102837358 | |||||
| chr12:102837862
|
A | T | 1 | a0001c0002t0020 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1313T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 1313 | chr12 | 102837862 | |||||
| chr12:102837869
|
T | TG | 5 | a0001c0001t0011a0001c0002t0011a0001c0003t0014others(2): Show | 7 | HG01175.hp1 HG01258.hp2 HG02055.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1305dupC | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 1305 | chr12 | 102837869 | |||||
| chr12:102837873
|
G | A | 1 | a0001c0002t0021 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1302C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 1302 | chr12 | 102837873 | |||||
| chr12:102837897
|
G | A | 4 | a0001c0004t0026a0001c0007t0010a0001c0008t0023others(1): Show | 6 | HG01175.hp2 HG01884.hp2 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1278C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 1278 | chr12 | 102837897 | |||||
| chr12:102837946
|
A | C | 1 | a0001c0004t0008 | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1229T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 1229 | chr12 | 102837946 | |||||
| chr12:102837951
|
C | T | 1 | a0001c0002t0019 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1224G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 1224 | chr12 | 102837951 | |||||
| chr12:102838086
|
T | A | 2 | a0001c0008t0018a0001c0009t0013 | 3 | HG01496.hp1 HG02109.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1089A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 1089 | chr12 | 102838086 | |||||
| chr12:102838119
|
T | A | 1 | a0001c0001t0025 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1056A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 1056 | chr12 | 102838119 | |||||
| chr12:102838157
|
C | T | 1 | a0001c0001t0025 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1018G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 1018 | chr12 | 102838157 | |||||
| chr12:102838314
|
A | G | 1 | a0001c0006t0016 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*861T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 861 | chr12 | 102838314 | |||||
| chr12:102838399
|
TTTAC | T | 1 | a0001c0001t0006 | 4 | HG02647.hp1 HG03225.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*772_*775delGTAA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 772 | chr12 | 102838399 | |||||
| chr12:102838523
|
G | C | 1 | a0001c0002t0022 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*652C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 652 | chr12 | 102838523 | |||||
| chr12:102838988
|
C | T | 25 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(22): Show | 103 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*187G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 187 | chr12 | 102838988 | |||||
| chr12:102839047
|
C | T | 1 | a0001c0006t0016 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*128G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 13/13 | 128 | chr12 | 102839047 | |||||
| chr12:102917139
|
C | G | 1 | a0001c0002t0015 | 1 | NA19067.hp2 | 5_prime_UTR_variant | MODIFIER | c.-9G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/13 | 9 | chr12 | 102917139 | |||||
| chr12:102917201
|
T | G | 16 | a0001c0001t0003a0001c0001t0004a0001c0001t0025others(13): Show | 69 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(66): Show |
5_prime_UTR_variant | MODIFIER | c.-71A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/13 | 71 | chr12 | 102917201 | |||||
| chr12:102917211
|
G | A | 3 | a0001c0001t0009a0001c0004t0008a0001c0004t0026 | 9 | HG00639.hp1 HG00741.hp2 HG01175.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-81C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/13 | 81 | chr12 | 102917211 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:102839253
|
G | A | 4 | a0001c0001t0002g0168a0001c0001t0002g0170a0001c0001t0002g0171others(1): Show | 4 | HG00639.hp2 HG01069.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1316-35C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102839253 | ||||||
| chr12:102839385
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1316-167C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102839385 | ||||||
| chr12:102839404
|
C | A | 1 | a0001c0001t0009g0306 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1316-186G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102839404 | ||||||
| chr12:102839455
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1316-237G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102839455 | ||||||
| chr12:102839465
|
C | A | 5 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0210others(2): Show | 5 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316-247G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102839465 | ||||||
| chr12:102839504
|
T | G | 4 | a0001c0003t0003g0287a0001c0003t0003g0288a0001c0003t0003g0289others(1): Show | 4 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(1): Show |
intron_variant | MODIFIER | c.1316-286A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102839504 | ||||||
| chr12:102839683
|
T | G | 9 | a0001c0001t0001g0028a0001c0004t0001g0103a0001c0004t0001g0140others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316-465A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102839683 | ||||||
| chr12:102839698
|
T | C | 80 | a0001c0001t0001g0046a0001c0001t0001g0070a0001c0001t0001g0127others(77): Show | 82 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1316-480A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102839698 | ||||||
| chr12:102839961
|
C | A | 1 | a0001c0001t0001g0024 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1315+439G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102839961 | ||||||
| chr12:102840040
|
G | A | 24 | a0001c0001t0001g0018a0001c0001t0002g0197a0001c0001t0002g0210others(21): Show | 24 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1315+360C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102840040 | ||||||
| chr12:102840058
|
T | C | 3 | a0001c0001t0007g0016a0001c0001t0007g0017a0001c0003t0005g0260 | 3 | HG02559.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1315+342A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102840058 | ||||||
| chr12:102840236
|
TG | T | 8 | a0001c0001t0002g0004a0001c0001t0002g0013a0001c0001t0002g0151others(5): Show | 9 | HG00741.hp1 HG01081.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1315+163delC | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102840236 | ||||||
| chr12:102840331
|
C | T | 11 | a0001c0001t0001g0028a0001c0001t0001g0054a0001c0001t0001g0071others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1315+69G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102840331 | ||||||
| chr12:102840380
|
G | A | 3 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228 | 3 | HG02630.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1315+20C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 12/12 | chr12 | 102840380 | ||||||
| chr12:102840701
|
A | G | 255 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(252): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1200-186T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102840701 | ||||||
| chr12:102840766
|
G | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(45): Show | 49 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1200-251C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102840766 | ||||||
| chr12:102840770
|
G | C | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1200-255C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102840770 | ||||||
| chr12:102840859
|
G | T | 1 | a0001c0001t0001g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1200-344C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102840859 | ||||||
| chr12:102840883
|
C | T | 3 | a0001c0007t0010g0031a0001c0007t0010g0032a0001c0007t0010g0033 | 3 | HG02280.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1200-368G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102840883 | ||||||
| chr12:102841047
|
A | G | 2 | a0001c0008t0023g0242a0001c0008t0024g0241 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1200-532T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841047 | ||||||
| chr12:102841258
|
T | G | 7 | a0001c0001t0007g0015a0001c0009t0005g0235a0001c0009t0005g0236others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200-743A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841258 | ||||||
| chr12:102841280
|
C | G | 14 | a0001c0004t0001g0103a0001c0004t0001g0140a0001c0004t0001g0141others(11): Show | 14 | HG01109.hp1 HG01243.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1200-765G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841280 | ||||||
| chr12:102841283
|
G | C | 1 | a0001c0001t0001g0203 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1200-768C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841283 | ||||||
| chr12:102841344
|
C | A | 14 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(11): Show | 14 | HG01891.hp1 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1200-829G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841344 | ||||||
| chr12:102841385
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1200-870T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841385 | ||||||
| chr12:102841534
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0002g0188 | 2 | HG02698.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1200-1019C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841534 | ||||||
| chr12:102841593
|
T | C | 1 | a0001c0002t0011g0089 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1200-1078A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841593 | ||||||
| chr12:102841606
|
T | G | 1 | a0001c0001t0004g0294 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1200-1091A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841606 | ||||||
| chr12:102841656
|
C | T | 250 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(247): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1200-1141G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841656 | ||||||
| chr12:102841660
|
C | T | 1 | a0001c0002t0011g0030 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1200-1145G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841660 | ||||||
| chr12:102841706
|
A | G | 1 | a0001c0006t0002g0211 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1200-1191T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841706 | ||||||
| chr12:102841797
|
C | T | 1 | a0001c0003t0003g0291 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1200-1282G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841797 | ||||||
| chr12:102841816
|
G | C | 18 | a0001c0004t0001g0103a0001c0004t0001g0140a0001c0004t0001g0141others(15): Show | 18 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1200-1301C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841816 | ||||||
| chr12:102841866
|
T | G | 1 | a0001c0001t0002g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1200-1351A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102841866 | ||||||
| chr12:102842167
|
G | A | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1199+1479C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102842167 | ||||||
| chr12:102842168
|
G | C | 2 | a0001c0001t0002g0173a0001c0001t0002g0174 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1199+1478C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102842168 | ||||||
| chr12:102842250
|
C | T | 8 | a0001c0001t0007g0015a0001c0006t0001g0213a0001c0009t0005g0235others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1199+1396G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102842250 | ||||||
| chr12:102842311
|
A | G | 3 | a0001c0007t0002g0040a0001c0007t0017g0043a0001c0015t0002g0148 | 3 | HG02109.hp2 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1199+1335T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102842311 | ||||||
| chr12:102842456
|
AAAAG | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131 | 3 | HG01884.hp1 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1199+1186_1199+118 others(8): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102842456 | ||||||
| chr12:102842473
|
T | A | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1199+1173A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102842473 | ||||||
| chr12:102842477
|
C | T | 8 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1199+1169G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102842477 | ||||||
| chr12:102842507
|
C | G | 1 | a0001c0001t0004g0262 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1199+1139G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102842507 | ||||||
| chr12:102842532
|
T | C | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1199+1114A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102842532 | ||||||
| chr12:102842755
|
T | G | 7 | a0001c0007t0010g0031a0001c0007t0010g0032a0001c0007t0010g0033others(4): Show | 7 | HG01496.hp1 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1199+891A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102842755 | ||||||
| chr12:102843044
|
T | C | 1 | a0001c0001t0006g0230 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1199+602A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102843044 | ||||||
| chr12:102843072
|
T | C | 3 | a0001c0007t0002g0040a0001c0007t0017g0043a0001c0015t0002g0148 | 3 | HG02109.hp2 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1199+574A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102843072 | ||||||
| chr12:102843382
|
C | T | 76 | a0001c0002t0001g0003a0001c0002t0001g0021a0001c0002t0001g0027others(73): Show | 78 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1199+264G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102843382 | ||||||
| chr12:102843422
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1199+224C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102843422 | ||||||
| chr12:102843467
|
G | A | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1199+179C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102843467 | ||||||
| chr12:102843488
|
C | T | 1 | a0001c0002t0001g0076 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1199+158G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 11/12 | chr12 | 102843488 | ||||||
| chr12:102843972
|
C | G | 70 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(67): Show | 71 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1066-193G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 10/12 | chr12 | 102843972 | ||||||
| chr12:102844015
|
G | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(58): Show | 63 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1066-236C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 10/12 | chr12 | 102844015 | ||||||
| chr12:102844131
|
T | A | 84 | a0001c0001t0001g0018a0001c0002t0001g0003a0001c0002t0001g0021others(81): Show | 86 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1065+205A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 10/12 | chr12 | 102844131 | ||||||
| chr12:102844180
|
A | C | 70 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(67): Show | 71 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1065+156T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 10/12 | chr12 | 102844180 | ||||||
| chr12:102844181
|
A | G | 70 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(67): Show | 71 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1065+155T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 10/12 | chr12 | 102844181 | ||||||
| chr12:102844239
|
C | T | 84 | a0001c0001t0001g0018a0001c0002t0001g0003a0001c0002t0001g0021others(81): Show | 86 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1065+97G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 10/12 | chr12 | 102844239 | ||||||
| chr12:102844276
|
A | G | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1065+60T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 10/12 | chr12 | 102844276 | ||||||
| chr12:102844541
|
GTGTCTA | G | 88 | a0001c0001t0001g0018a0001c0002t0001g0003a0001c0002t0001g0021others(85): Show | 90 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.970-116_970-111del others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102844541 | ||||||
| chr12:102844626
|
C | T | 84 | a0001c0001t0001g0018a0001c0002t0001g0003a0001c0002t0001g0021others(81): Show | 86 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.970-195G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102844626 | ||||||
| chr12:102844735
|
A | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0067a0001c0001t0001g0159 | 3 | HG00642.hp1 HG01106.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.970-304T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102844735 | ||||||
| chr12:102844922
|
A | G | 1 | a0001c0002t0001g0081 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.970-491T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102844922 | ||||||
| chr12:102844924
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.970-493G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102844924 | ||||||
| chr12:102845011
|
A | C | 10 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(7): Show | 10 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.970-580T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102845011 | ||||||
| chr12:102845061
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.970-630G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102845061 | ||||||
| chr12:102845171
|
T | C | 76 | a0001c0002t0001g0003a0001c0002t0001g0021a0001c0002t0001g0027others(73): Show | 78 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.970-740A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102845171 | ||||||
| chr12:102845191
|
A | G | 1 | a0001c0001t0002g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.970-760T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102845191 | ||||||
| chr12:102845244
|
G | T | 1 | a0005c0017t0001g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.970-813C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102845244 | ||||||
| chr12:102845274
|
C | T | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.970-843G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102845274 | ||||||
| chr12:102845283
|
A | T | 255 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(252): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.970-852T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102845283 | ||||||
| chr12:102845414
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(236): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.970-983G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102845414 | ||||||
| chr12:102845653
|
T | A | 1 | a0001c0001t0001g0207 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.970-1222A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102845653 | ||||||
| chr12:102845730
|
C | A | 2 | a0001c0002t0001g0062a0001c0002t0015g0007 | 2 | NA18977.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.969+1165G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102845730 | ||||||
| chr12:102845831
|
T | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(237): Show | 245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.969+1064A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102845831 | ||||||
| chr12:102845858
|
C | T | 2 | a0001c0008t0023g0242a0001c0008t0024g0241 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.969+1037G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102845858 | ||||||
| chr12:102846012
|
T | A | 1 | a0001c0002t0001g0153 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.969+883A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102846012 | ||||||
| chr12:102846141
|
A | C | 1 | a0001c0001t0003g0233 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.969+754T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102846141 | ||||||
| chr12:102846289
|
C | T | 83 | a0001c0001t0001g0018a0001c0002t0001g0003a0001c0002t0001g0021others(80): Show | 85 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.969+606G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102846289 | ||||||
| chr12:102846374
|
C | T | 4 | a0001c0001t0006g0226a0001c0001t0006g0227a0001c0001t0006g0229others(1): Show | 4 | HG02647.hp1 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.969+521G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102846374 | ||||||
| chr12:102846674
|
A | C | 70 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(67): Show | 71 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.969+221T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102846674 | ||||||
| chr12:102846692
|
A | G | 1 | a0001c0002t0001g0175 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.969+203T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102846692 | ||||||
| chr12:102846852
|
C | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(59): Show | 64 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.969+43G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102846852 | ||||||
| chr12:102846875
|
C | T | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.969+20G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 9/12 | chr12 | 102846875 | ||||||
| chr12:102847039
|
G | C | 2 | a0001c0004t0002g0150a0001c0004t0007g0145 | 2 | HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.913-88C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102847039 | ||||||
| chr12:102847292
|
T | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(237): Show | 245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.913-341A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102847292 | ||||||
| chr12:102847294
|
T | C | 10 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0013others(7): Show | 11 | HG00741.hp1 HG01081.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.913-343A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102847294 | ||||||
| chr12:102847377
|
G | A | 4 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228others(1): Show | 4 | HG01496.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.913-426C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102847377 | ||||||
| chr12:102847410
|
A | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(51): Show | 55 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.913-459T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102847410 | ||||||
| chr12:102847501
|
T | C | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.913-550A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102847501 | ||||||
| chr12:102847554
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.913-603T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102847554 | ||||||
| chr12:102847903
|
C | A | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.913-952G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102847903 | ||||||
| chr12:102847993
|
A | G | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.913-1042T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102847993 | ||||||
| chr12:102848127
|
C | G | 255 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(252): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.913-1176G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848127 | ||||||
| chr12:102848135
|
A | G | 255 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(252): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.913-1184T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848135 | ||||||
| chr12:102848168
|
CAGGACAC others(29): Show |
C | 79 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(76): Show | 80 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.913-1253_913-1218d others(38): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848168 | ||||||
| chr12:102848267
|
AGGACACC others(98): Show |
A | 19 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(16): Show | 19 | HG01496.hp1 HG01891.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.913-1421_913-1317d others(2): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848267 | ||||||
| chr12:102848279
|
G | C | 1 | a0001c0004t0001g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.913-1328C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848279 | ||||||
| chr12:102848283
|
G | A | 1 | a0001c0004t0001g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.913-1332C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848283 | ||||||
| chr12:102848286
|
G | A | 1 | a0001c0004t0001g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.913-1335C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848286 | ||||||
| chr12:102848290
|
T | C | 1 | a0001c0004t0001g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.913-1339A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848290 | ||||||
| chr12:102848291
|
TAAGTGTA others(168): Show |
T | 1 | a0001c0004t0001g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.913-1515_913-1341d others(2): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848291 | ||||||
| chr12:102848319
|
GAGAGGTG others(28): Show |
G | 79 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(76): Show | 80 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.913-1403_913-1369d others(37): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848319 | ||||||
| chr12:102848391
|
A | G | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.913-1440T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848391 | ||||||
| chr12:102848407
|
GGGACACC others(63): Show |
G | 70 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(67): Show | 71 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.913-1526_913-1457d others(72): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848407 | ||||||
| chr12:102848470
|
G | T | 1 | a0001c0004t0001g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.913-1519C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848470 | ||||||
| chr12:102848477
|
A | G | 1 | a0001c0004t0001g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.913-1526T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848477 | ||||||
| chr12:102848500
|
T | C | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1549A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848500 | ||||||
| chr12:102848505
|
G | T | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1554C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848505 | ||||||
| chr12:102848506
|
A | G | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1555T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848506 | ||||||
| chr12:102848518
|
C | T | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1567G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848518 | ||||||
| chr12:102848536
|
G | T | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1585C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848536 | ||||||
| chr12:102848551
|
C | T | 1 | a0001c0002t0001g0185 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.913-1600G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848551 | ||||||
| chr12:102848559
|
G | C | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1608C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848559 | ||||||
| chr12:102848570
|
C | T | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1619G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848570 | ||||||
| chr12:102848571
|
T | A | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1620A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848571 | ||||||
| chr12:102848575
|
T | G | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1624A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848575 | ||||||
| chr12:102848579
|
G | A | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1628C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848579 | ||||||
| chr12:102848588
|
T | C | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1637A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848588 | ||||||
| chr12:102848596
|
C | A | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1645G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848596 | ||||||
| chr12:102848605
|
T | C | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1654A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848605 | ||||||
| chr12:102848610
|
G | T | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1659C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848610 | ||||||
| chr12:102848618
|
A | G | 164 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(161): Show | 167 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.913-1667T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848618 | ||||||
| chr12:102848631
|
CTGGAGAG others(28): Show |
C | 79 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(76): Show | 80 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.913-1715_913-1681d others(37): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848631 | ||||||
| chr12:102848640
|
T | C | 5 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-1689A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848640 | ||||||
| chr12:102848641
|
A | G | 5 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-1690T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848641 | ||||||
| chr12:102848645
|
G | A | 5 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-1694C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848645 | ||||||
| chr12:102848649
|
A | G | 5 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-1698T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848649 | ||||||
| chr12:102848666
|
A | C | 5 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-1715T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848666 | ||||||
| chr12:102848675
|
C | T | 5 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-1724G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848675 | ||||||
| chr12:102848676
|
T | A | 1 | a0001c0001t0009g0306 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.913-1725A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848676 | ||||||
| chr12:102848676
|
T | G | 78 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(75): Show | 79 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.913-1725A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848676 | ||||||
| chr12:102848680
|
T | A | 79 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(76): Show | 80 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.913-1729A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848680 | ||||||
| chr12:102848680
|
T | G | 5 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-1729A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848680 | ||||||
| chr12:102848689
|
G | T | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.913-1738C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848689 | ||||||
| chr12:102848690
|
A | T | 5 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-1739T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848690 | ||||||
| chr12:102848699
|
C | G | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1748G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848699 | ||||||
| chr12:102848710
|
C | T | 86 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(83): Show | 88 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.913-1759G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848710 | ||||||
| chr12:102848711
|
G | A | 5 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-1760C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848711 | ||||||
| chr12:102848711
|
G | T | 79 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(76): Show | 80 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.913-1760C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848711 | ||||||
| chr12:102848715
|
A | G | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-1764T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848715 | ||||||
| chr12:102848719
|
G | A | 5 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-1768C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848719 | ||||||
| chr12:102848721
|
C | G | 2 | a0001c0001t0012g0146a0001c0001t0012g0190 | 2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.913-1770G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848721 | ||||||
| chr12:102848725
|
A | T | 79 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(76): Show | 80 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.913-1774T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848725 | ||||||
| chr12:102848746
|
T | A | 79 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(76): Show | 80 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.913-1795A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848746 | ||||||
| chr12:102848754
|
G | A | 79 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(76): Show | 80 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.913-1803C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848754 | ||||||
| chr12:102848760
|
T | A | 79 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(76): Show | 80 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.913-1809A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848760 | ||||||
| chr12:102848842
|
C | T | 15 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(12): Show | 15 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.913-1891G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102848842 | ||||||
| chr12:102849000
|
CAG | C | 3 | a0001c0003t0001g0048a0001c0003t0001g0049a0001c0003t0001g0050 | 3 | NA18942.hp2 NA19067.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.913-2051_913-2050d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849000 | ||||||
| chr12:102849065
|
C | T | 4 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228others(1): Show | 4 | HG01496.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.913-2114G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849065 | ||||||
| chr12:102849210
|
G | C | 2 | a0001c0008t0023g0242a0001c0008t0024g0241 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.913-2259C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849210 | ||||||
| chr12:102849273
|
C | T | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.913-2322G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849273 | ||||||
| chr12:102849396
|
A | AT | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.912+2290dupA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849396 | ||||||
| chr12:102849399
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(145): Show | 151 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.912+2288G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849399 | ||||||
| chr12:102849467
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.912+2220C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849467 | ||||||
| chr12:102849577
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(61): Show | 66 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.912+2110A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849577 | ||||||
| chr12:102849578
|
A | G | 2 | a0001c0008t0023g0242a0001c0008t0024g0241 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.912+2109T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849578 | ||||||
| chr12:102849579
|
T | C | 1 | a0001c0001t0002g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.912+2108A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849579 | ||||||
| chr12:102849785
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.912+1902C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849785 | ||||||
| chr12:102849798
|
C | T | 1 | a0001c0001t0007g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.912+1889G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849798 | ||||||
| chr12:102849823
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(61): Show | 66 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.912+1864C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849823 | ||||||
| chr12:102849829
|
T | C | 84 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(81): Show | 85 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.912+1858A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849829 | ||||||
| chr12:102849999
|
C | T | 1 | a0001c0003t0003g0291 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.912+1688G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102849999 | ||||||
| chr12:102850044
|
T | C | 1 | a0001c0001t0002g0192 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.912+1643A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102850044 | ||||||
| chr12:102850062
|
G | A | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.912+1625C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102850062 | ||||||
| chr12:102850105
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.912+1582A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102850105 | ||||||
| chr12:102850235
|
G | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(156): Show | 162 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.912+1452C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102850235 | ||||||
| chr12:102850301
|
A | C | 1 | a0001c0001t0001g0162 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.912+1386T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102850301 | ||||||
| chr12:102850542
|
T | G | 10 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0013others(7): Show | 11 | HG00741.hp1 HG01081.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.912+1145A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102850542 | ||||||
| chr12:102850898
|
A | G | 3 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228 | 3 | HG02630.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.912+789T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102850898 | ||||||
| chr12:102850900
|
G | A | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.912+787C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102850900 | ||||||
| chr12:102851033
|
G | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.912+654C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102851033 | ||||||
| chr12:102851043
|
C | T | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.912+644G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102851043 | ||||||
| chr12:102851088
|
T | TA | 90 | a0001c0001t0001g0018a0001c0001t0001g0159a0001c0001t0001g0179others(87): Show | 92 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.912+598dupT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102851088 | ||||||
| chr12:102851088
|
T | TAA | 65 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(62): Show | 66 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.912+597_912+598dup others(2): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102851088 | ||||||
| chr12:102851093
|
G | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.912+594C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102851093 | ||||||
| chr12:102851458
|
G | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0161a0001c0001t0002g0180others(12): Show | 16 | HG00323.hp1 HG01099.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.912+229C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 8/12 | chr12 | 102851458 | ||||||
| chr12:102852023
|
C | T | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.843-267G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852023 | ||||||
| chr12:102852024
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.843-268T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852024 | ||||||
| chr12:102852076
|
T | C | 11 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.843-320A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852076 | ||||||
| chr12:102852083
|
C | A | 5 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-327G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852083 | ||||||
| chr12:102852280
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.843-524C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852280 | ||||||
| chr12:102852308
|
A | C | 2 | a0001c0003t0003g0287a0001c0003t0003g0288 | 2 | HG00408.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.842+507T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852308 | ||||||
| chr12:102852395
|
A | G | 1 | a0001c0004t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.842+420T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852395 | ||||||
| chr12:102852483
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.842+332T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852483 | ||||||
| chr12:102852485
|
T | C | 1 | a0001c0002t0001g0039 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.842+330A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852485 | ||||||
| chr12:102852487
|
T | C | 2 | a0001c0003t0003g0263a0001c0003t0014g0279 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.842+328A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852487 | ||||||
| chr12:102852533
|
C | T | 11 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.842+282G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852533 | ||||||
| chr12:102852575
|
A | T | 1 | a0001c0003t0003g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.842+240T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852575 | ||||||
| chr12:102852614
|
C | A | 11 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.842+201G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852614 | ||||||
| chr12:102852623
|
C | T | 4 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228others(1): Show | 4 | HG01496.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.842+192G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 7/12 | chr12 | 102852623 | ||||||
| chr12:102852957
|
T | A | 11 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.707-7A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102852957 | ||||||
| chr12:102853097
|
C | G | 1 | a0001c0002t0001g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.707-147G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102853097 | ||||||
| chr12:102853339
|
G | A | 1 | a0001c0003t0003g0272 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.707-389C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102853339 | ||||||
| chr12:102853557
|
C | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0207 | 3 | HG01358.hp1 NA18942.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.707-607G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102853557 | ||||||
| chr12:102853577
|
A | G | 10 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0013others(7): Show | 11 | HG00741.hp1 HG01081.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.707-627T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102853577 | ||||||
| chr12:102853705
|
G | A | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.707-755C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102853705 | ||||||
| chr12:102853708
|
T | C | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0138 | 3 | HG01074.hp1 HG01255.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.707-758A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102853708 | ||||||
| chr12:102853772
|
A | G | 1 | a0001c0001t0009g0299 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.707-822T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102853772 | ||||||
| chr12:102853786
|
T | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(79): Show | 84 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.707-836A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102853786 | ||||||
| chr12:102853855
|
A | G | 4 | a0001c0003t0003g0257a0001c0003t0003g0263a0001c0003t0003g0270others(1): Show | 4 | HG00735.hp1 HG01081.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.707-905T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102853855 | ||||||
| chr12:102853875
|
A | T | 77 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(74): Show | 78 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.707-925T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102853875 | ||||||
| chr12:102853889
|
G | A | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.707-939C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102853889 | ||||||
| chr12:102854058
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(61): Show | 66 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.706+1078T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102854058 | ||||||
| chr12:102854239
|
T | G | 77 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(74): Show | 78 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.706+897A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102854239 | ||||||
| chr12:102854284
|
C | G | 11 | a0001c0004t0001g0103a0001c0004t0001g0140a0001c0004t0001g0141others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.706+852G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102854284 | ||||||
| chr12:102854329
|
C | T | 4 | a0001c0001t0002g0004a0001c0001t0002g0151a0001c0001t0002g0152others(1): Show | 5 | HG00741.hp1 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.706+807G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102854329 | ||||||
| chr12:102854362
|
G | C | 3 | a0001c0007t0010g0031a0001c0007t0010g0032a0001c0007t0010g0033 | 3 | HG02280.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.706+774C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102854362 | ||||||
| chr12:102854494
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.706+642T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102854494 | ||||||
| chr12:102854523
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.706+613A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102854523 | ||||||
| chr12:102854656
|
T | C | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.706+480A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102854656 | ||||||
| chr12:102854685
|
T | C | 255 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(252): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.706+451A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102854685 | ||||||
| chr12:102854701
|
A | G | 3 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228 | 3 | HG02630.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.706+435T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102854701 | ||||||
| chr12:102854810
|
C | CAAACAAA others(3): Show |
1 | a0001c0002t0001g0094 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.706+316_706+325dup others(10): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102854810 | ||||||
| chr12:102854834
|
A | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(66): Show | 71 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.706+302T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102854834 | ||||||
| chr12:102855080
|
C | T | 11 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.706+56G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 6/12 | chr12 | 102855080 | ||||||
| chr12:102855378
|
C | T | 1 | a0001c0001t0007g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.510-46G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102855378 | ||||||
| chr12:102855386
|
C | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(51): Show | 55 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.510-54G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102855386 | ||||||
| chr12:102855540
|
G | A | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.510-208C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102855540 | ||||||
| chr12:102855549
|
G | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(252): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.510-217C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102855549 | ||||||
| chr12:102855585
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.510-253G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102855585 | ||||||
| chr12:102855586
|
G | A | 7 | a0001c0006t0001g0213a0001c0009t0005g0235a0001c0009t0005g0236others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-254C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102855586 | ||||||
| chr12:102855635
|
G | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(161): Show | 167 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.510-303C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102855635 | ||||||
| chr12:102855654
|
C | G | 1 | a0001c0001t0002g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.510-322G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102855654 | ||||||
| chr12:102855659
|
C | T | 7 | a0001c0006t0001g0213a0001c0009t0005g0235a0001c0009t0005g0236others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-327G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102855659 | ||||||
| chr12:102855846
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.510-514C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102855846 | ||||||
| chr12:102855873
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG00558.hp1 NA18966.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-541C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102855873 | ||||||
| chr12:102856008
|
T | TAATTATA others(28): Show |
8 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.510-711_510-677dup others(35): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856008 | ||||||
| chr12:102856047
|
TATA | T | 77 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(74): Show | 78 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.510-718_510-716del others(3): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856047 | ||||||
| chr12:102856061
|
A | G | 14 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.510-729T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856061 | ||||||
| chr12:102856078
|
C | CTAAA | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.510-750_510-747dup others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856078 | ||||||
| chr12:102856129
|
GA | G | 9 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.510-798delT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856129 | ||||||
| chr12:102856174
|
C | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(79): Show | 84 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.510-842G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856174 | ||||||
| chr12:102856192
|
A | G | 1 | a0001c0002t0001g0080 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.510-860T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856192 | ||||||
| chr12:102856212
|
C | G | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-880G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856212 | ||||||
| chr12:102856260
|
T | C | 9 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.510-928A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856260 | ||||||
| chr12:102856300
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510-968G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856300 | ||||||
| chr12:102856333
|
G | A | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-1001C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856333 | ||||||
| chr12:102856337
|
A | T | 1 | a0001c0002t0003g0231 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.510-1005T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856337 | ||||||
| chr12:102856467
|
A | T | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.510-1135T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856467 | ||||||
| chr12:102856520
|
C | T | 54 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(51): Show | 55 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.510-1188G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856520 | ||||||
| chr12:102856522
|
T | C | 6 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(3): Show | 6 | HG01433.hp1 HG01928.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-1190A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856522 | ||||||
| chr12:102856604
|
G | A | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.510-1272C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856604 | ||||||
| chr12:102856609
|
C | T | 1 | a0001c0011t0002g0069 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.510-1277G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856609 | ||||||
| chr12:102856610
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.510-1278C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856610 | ||||||
| chr12:102856682
|
T | C | 110 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(107): Show | 112 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.510-1350A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856682 | ||||||
| chr12:102856775
|
G | A | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.510-1443C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856775 | ||||||
| chr12:102856801
|
A | G | 1 | a0001c0006t0001g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-1469T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856801 | ||||||
| chr12:102856878
|
G | A | 3 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228 | 3 | HG02630.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.510-1546C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856878 | ||||||
| chr12:102856934
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.510-1602C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856934 | ||||||
| chr12:102856955
|
C | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 70 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.510-1623G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102856955 | ||||||
| chr12:102857151
|
A | G | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-1819T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857151 | ||||||
| chr12:102857324
|
G | A | 1 | a0001c0004t0001g0147 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.510-1992C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857324 | ||||||
| chr12:102857343
|
C | A | 1 | a0001c0001t0003g0233 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.510-2011G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857343 | ||||||
| chr12:102857393
|
C | T | 1 | a0001c0001t0025g0234 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.510-2061G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857393 | ||||||
| chr12:102857411
|
C | T | 8 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.510-2079G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857411 | ||||||
| chr12:102857448
|
A | G | 70 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(67): Show | 71 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.510-2116T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857448 | ||||||
| chr12:102857528
|
C | T | 4 | a0001c0003t0001g0121a0001c0003t0003g0243a0001c0003t0003g0244others(1): Show | 4 | HG00597.hp2 HG02040.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-2196G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857528 | ||||||
| chr12:102857553
|
A | G | 1 | a0001c0002t0001g0123 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.510-2221T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857553 | ||||||
| chr12:102857628
|
G | T | 1 | a0001c0006t0004g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.510-2296C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857628 | ||||||
| chr12:102857645
|
C | G | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.510-2313G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857645 | ||||||
| chr12:102857717
|
A | C | 12 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(9): Show | 12 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-2385T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857717 | ||||||
| chr12:102857729
|
T | C | 2 | a0001c0008t0023g0242a0001c0008t0024g0241 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.510-2397A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857729 | ||||||
| chr12:102857795
|
T | G | 306 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(303): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.510-2463A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857795 | ||||||
| chr12:102857897
|
C | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(154): Show | 160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.510-2565G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857897 | ||||||
| chr12:102857914
|
A | G | 2 | a0001c0001t0002g0009a0001c0001t0002g0010 | 2 | HG01167.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.510-2582T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102857914 | ||||||
| chr12:102858006
|
C | A | 1 | a0001c0003t0003g0283 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.510-2674G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858006 | ||||||
| chr12:102858088
|
G | A | 1 | a0001c0003t0003g0267 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.510-2756C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858088 | ||||||
| chr12:102858152
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.510-2820A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858152 | ||||||
| chr12:102858184
|
T | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.510-2852A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858184 | ||||||
| chr12:102858202
|
A | G | 4 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228others(1): Show | 4 | HG01496.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-2870T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858202 | ||||||
| chr12:102858210
|
T | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.510-2878A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858210 | ||||||
| chr12:102858214
|
A | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.510-2882T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858214 | ||||||
| chr12:102858287
|
G | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 70 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.510-2955C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858287 | ||||||
| chr12:102858355
|
A | T | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.510-3023T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858355 | ||||||
| chr12:102858381
|
C | T | 2 | a0001c0001t0004g0285a0001c0001t0004g0286 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.510-3049G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858381 | ||||||
| chr12:102858436
|
G | A | 1 | a0001c0002t0020g0078 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.510-3104C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858436 | ||||||
| chr12:102858548
|
T | A | 1 | a0001c0003t0003g0273 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.510-3216A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858548 | ||||||
| chr12:102858595
|
T | G | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.510-3263A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858595 | ||||||
| chr12:102858609
|
A | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.510-3277T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858609 | ||||||
| chr12:102858652
|
G | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(161): Show | 167 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.510-3320C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858652 | ||||||
| chr12:102858693
|
G | C | 2 | a0001c0001t0002g0009a0001c0001t0002g0010 | 2 | HG01167.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.510-3361C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858693 | ||||||
| chr12:102858757
|
G | A | 7 | a0001c0002t0001g0075a0001c0002t0001g0084a0001c0002t0001g0092others(4): Show | 7 | HG01257.hp1 HG01496.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-3425C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858757 | ||||||
| chr12:102858760
|
G | A | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-3428C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858760 | ||||||
| chr12:102858833
|
G | A | 2 | a0001c0001t0001g0156a0001c0014t0003g0261 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.510-3501C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858833 | ||||||
| chr12:102858863
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.510-3531T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858863 | ||||||
| chr12:102858951
|
G | A | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.510-3619C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102858951 | ||||||
| chr12:102859013
|
C | CA | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-3682dupT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102859013 | ||||||
| chr12:102859152
|
G | A | 1 | a0001c0002t0001g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.510-3820C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102859152 | ||||||
| chr12:102859336
|
C | T | 2 | a0001c0002t0001g0038a0001c0002t0001g0058 | 2 | NA18944.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.510-4004G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102859336 | ||||||
| chr12:102859360
|
A | T | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0007t0002g0178 | 3 | HG02451.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.510-4028T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102859360 | ||||||
| chr12:102859379
|
G | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 70 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.510-4047C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102859379 | ||||||
| chr12:102859511
|
G | A | 10 | a0001c0004t0001g0103a0001c0004t0001g0141a0001c0004t0001g0143others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-4179C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102859511 | ||||||
| chr12:102859574
|
A | G | 3 | a0001c0007t0010g0031a0001c0007t0010g0032a0001c0007t0010g0033 | 3 | HG02280.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.510-4242T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102859574 | ||||||
| chr12:102859721
|
A | G | 1 | a0001c0003t0003g0267 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.510-4389T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102859721 | ||||||
| chr12:102859726
|
A | G | 10 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0013others(7): Show | 11 | HG00741.hp1 HG01081.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-4394T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102859726 | ||||||
| chr12:102859813
|
G | A | 1 | a0001c0015t0002g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.510-4481C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102859813 | ||||||
| chr12:102859968
|
G | A | 1 | a0001c0002t0011g0030 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.510-4636C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102859968 | ||||||
| chr12:102860006
|
C | G | 3 | a0001c0007t0010g0031a0001c0007t0010g0032a0001c0007t0010g0033 | 3 | HG02280.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.510-4674G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102860006 | ||||||
| chr12:102860007
|
G | A | 1 | a0001c0001t0002g0212 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.510-4675C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102860007 | ||||||
| chr12:102860020
|
GA | G | 10 | a0001c0004t0001g0103a0001c0004t0001g0141a0001c0004t0001g0143others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-4689delT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102860020 | ||||||
| chr12:102860116
|
T | G | 2 | a0001c0001t0002g0200a0001c0001t0002g0205 | 2 | HG01106.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.510-4784A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102860116 | ||||||
| chr12:102860353
|
G | A | 14 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0013others(11): Show | 15 | HG00741.hp1 HG01081.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.510-5021C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102860353 | ||||||
| chr12:102860504
|
C | CA | 164 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(161): Show | 167 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.510-5173dupT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102860504 | ||||||
| chr12:102860510
|
T | G | 164 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(161): Show | 167 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.510-5178A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102860510 | ||||||
| chr12:102860511
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.510-5179T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102860511 | ||||||
| chr12:102860516
|
G | A | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.510-5184C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102860516 | ||||||
| chr12:102860564
|
C | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(51): Show | 55 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.510-5232G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102860564 | ||||||
| chr12:102860573
|
C | A | 10 | a0001c0004t0001g0103a0001c0004t0001g0141a0001c0004t0001g0143others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-5241G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102860573 | ||||||
| chr12:102860858
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.510-5526A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102860858 | ||||||
| chr12:102860896
|
G | A | 14 | a0001c0004t0001g0103a0001c0004t0001g0141a0001c0004t0001g0143others(11): Show | 14 | HG01109.hp1 HG01243.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.510-5564C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102860896 | ||||||
| chr12:102861032
|
T | C | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+5564A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861032 | ||||||
| chr12:102861114
|
C | G | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.509+5482G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861114 | ||||||
| chr12:102861242
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.509+5354T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861242 | ||||||
| chr12:102861320
|
G | A | 5 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0038others(2): Show | 5 | NA18944.hp1 NA18963.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+5276C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861320 | ||||||
| chr12:102861388
|
G | T | 12 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(9): Show | 12 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.509+5208C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861388 | ||||||
| chr12:102861450
|
C | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(78): Show | 83 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.509+5146G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861450 | ||||||
| chr12:102861494
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.509+5102C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861494 | ||||||
| chr12:102861637
|
A | G | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+4959T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861637 | ||||||
| chr12:102861766
|
G | A | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.509+4830C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861766 | ||||||
| chr12:102861835
|
T | C | 255 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(252): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.509+4761A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861835 | ||||||
| chr12:102861843
|
G | A | 76 | a0001c0002t0001g0003a0001c0002t0001g0021a0001c0002t0001g0027others(73): Show | 78 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.509+4753C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861843 | ||||||
| chr12:102861849
|
G | T | 77 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(74): Show | 78 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.509+4747C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861849 | ||||||
| chr12:102861935
|
G | A | 8 | a0001c0001t0002g0216a0001c0001t0009g0305a0001c0001t0009g0306others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+4661C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861935 | ||||||
| chr12:102861966
|
T | TA | 12 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0002g0004others(9): Show | 13 | HG00741.hp1 HG01069.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.509+4629dupT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861966 | ||||||
| chr12:102861966
|
T | TAA | 26 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0026others(23): Show | 27 | HG00140.hp2 HG00738.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.509+4628_509+4629d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861966 | ||||||
| chr12:102861966
|
T | TAAA | 43 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.509+4627_509+4629d others(5): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861966 | ||||||
| chr12:102861966
|
T | TAAAA | 60 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0187others(57): Show | 61 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.509+4626_509+4629d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861966 | ||||||
| chr12:102861966
|
TA | T | 26 | a0001c0002t0001g0064a0001c0002t0001g0076a0001c0002t0001g0080others(23): Show | 26 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.509+4629delT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861966 | ||||||
| chr12:102861966
|
TAA | T | 15 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(12): Show | 15 | HG01496.hp1 HG01891.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.509+4628_509+4629d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861966 | ||||||
| chr12:102861970
|
A | T | 11 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.509+4626T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861970 | ||||||
| chr12:102861972
|
A | T | 8 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.509+4624T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861972 | ||||||
| chr12:102861986
|
A | G | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+4610T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102861986 | ||||||
| chr12:102862072
|
T | G | 1 | a0001c0004t0002g0150 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.509+4524A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102862072 | ||||||
| chr12:102862218
|
T | C | 255 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(252): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.509+4378A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102862218 | ||||||
| chr12:102862237
|
C | A | 8 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(5): Show | 8 | HG01167.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+4359G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102862237 | ||||||
| chr12:102862393
|
A | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(160): Show | 166 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.509+4203T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102862393 | ||||||
| chr12:102862572
|
A | T | 83 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(80): Show | 84 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.509+4024T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102862572 | ||||||
| chr12:102862573
|
A | T | 1 | a0001c0001t0002g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.509+4023T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102862573 | ||||||
| chr12:102862738
|
G | C | 70 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(67): Show | 71 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.509+3858C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102862738 | ||||||
| chr12:102862773
|
T | C | 76 | a0001c0002t0001g0003a0001c0002t0001g0021a0001c0002t0001g0027others(73): Show | 78 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.509+3823A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102862773 | ||||||
| chr12:102862784
|
T | C | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.509+3812A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102862784 | ||||||
| chr12:102862889
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.509+3707T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102862889 | ||||||
| chr12:102862946
|
G | GA | 67 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(64): Show | 69 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.509+3649dupT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102862946 | ||||||
| chr12:102862982
|
C | T | 11 | a0001c0002t0001g0027a0001c0002t0001g0061a0001c0002t0001g0064others(8): Show | 11 | NA18948.hp2 NA18954.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.509+3614G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102862982 | ||||||
| chr12:102862984
|
C | T | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+3612G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102862984 | ||||||
| chr12:102863441
|
G | C | 16 | a0001c0004t0001g0103a0001c0004t0001g0140a0001c0004t0001g0141others(13): Show | 16 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.509+3155C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102863441 | ||||||
| chr12:102863530
|
T | C | 163 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(160): Show | 166 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.509+3066A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102863530 | ||||||
| chr12:102863558
|
G | A | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+3038C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102863558 | ||||||
| chr12:102863598
|
A | T | 1 | a0001c0001t0009g0306 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.509+2998T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102863598 | ||||||
| chr12:102863621
|
G | A | 1 | a0001c0002t0001g0099 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.509+2975C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102863621 | ||||||
| chr12:102863763
|
G | C | 11 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.509+2833C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102863763 | ||||||
| chr12:102863824
|
A | T | 2 | a0001c0008t0023g0242a0001c0008t0024g0241 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.509+2772T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102863824 | ||||||
| chr12:102863826
|
A | C | 11 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.509+2770T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102863826 | ||||||
| chr12:102864098
|
A | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(143): Show | 149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.509+2498T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102864098 | ||||||
| chr12:102864124
|
C | T | 1 | a0001c0002t0001g0175 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.509+2472G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102864124 | ||||||
| chr12:102864805
|
C | CA | 19 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(16): Show | 19 | HG01496.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.509+1790dupT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102864805 | ||||||
| chr12:102864805
|
C | CAA | 77 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(74): Show | 78 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.509+1789_509+1790d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102864805 | ||||||
| chr12:102864805
|
C | CAAA | 69 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(66): Show | 71 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.509+1788_509+1790d others(5): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102864805 | ||||||
| chr12:102864902
|
T | C | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.509+1694A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102864902 | ||||||
| chr12:102865145
|
T | G | 77 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(74): Show | 78 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.509+1451A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102865145 | ||||||
| chr12:102865170
|
T | C | 1 | a0001c0009t0005g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.509+1426A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102865170 | ||||||
| chr12:102865501
|
A | G | 76 | a0001c0001t0001g0070a0001c0002t0001g0003a0001c0002t0001g0021others(73): Show | 78 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.509+1095T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102865501 | ||||||
| chr12:102865757
|
C | T | 1 | a0001c0009t0005g0235 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.509+839G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102865757 | ||||||
| chr12:102865809
|
T | A | 4 | a0001c0003t0003g0287a0001c0003t0003g0288a0001c0003t0003g0289others(1): Show | 4 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+787A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102865809 | ||||||
| chr12:102865920
|
A | C | 4 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228others(1): Show | 4 | HG01496.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+676T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102865920 | ||||||
| chr12:102866051
|
AG | A | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+544delC | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866051 | ||||||
| chr12:102866070
|
G | A | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+526C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866070 | ||||||
| chr12:102866075
|
C | G | 16 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(13): Show | 16 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+521G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866075 | ||||||
| chr12:102866083
|
G | GA | 20 | a0001c0002t0001g0051a0001c0003t0003g0269a0001c0003t0003g0283others(17): Show | 20 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.509+512dupT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866083 | ||||||
| chr12:102866083
|
G | GAAA | 16 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(13): Show | 16 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+510_509+512dup others(3): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866083 | ||||||
| chr12:102866083
|
G | GAAAA | 62 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(59): Show | 64 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.509+509_509+512dup others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866083 | ||||||
| chr12:102866096
|
C | A | 4 | a0001c0006t0002g0211a0001c0006t0004g0292a0001c0006t0004g0293others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+500G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866096 | ||||||
| chr12:102866253
|
T | C | 2 | a0001c0006t0002g0211a0001c0006t0004g0297 | 2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.509+343A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866253 | ||||||
| chr12:102866280
|
T | A | 2 | a0001c0001t0012g0146a0001c0001t0012g0190 | 2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.509+316A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866280 | ||||||
| chr12:102866371
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.509+225T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866371 | ||||||
| chr12:102866441
|
A | C | 15 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0013others(12): Show | 16 | HG00741.hp1 HG01081.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+155T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866441 | ||||||
| chr12:102866456
|
C | T | 2 | a0001c0006t0002g0211a0001c0006t0004g0297 | 2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.509+140G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866456 | ||||||
| chr12:102866495
|
T | G | 75 | a0001c0002t0001g0003a0001c0002t0001g0021a0001c0002t0001g0027others(72): Show | 77 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.509+101A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866495 | ||||||
| chr12:102866543
|
C | A | 1 | a0001c0001t0002g0196 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.509+53G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 5/12 | chr12 | 102866543 | ||||||
| chr12:102866695
|
G | C | 3 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228 | 3 | HG02630.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.442-32C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102866695 | ||||||
| chr12:102866830
|
T | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(64): Show | 69 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.442-167A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102866830 | ||||||
| chr12:102866856
|
T | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(78): Show | 83 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.442-193A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102866856 | ||||||
| chr12:102866886
|
G | A | 14 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(11): Show | 14 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.442-223C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102866886 | ||||||
| chr12:102866972
|
T | C | 14 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(11): Show | 14 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.442-309A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102866972 | ||||||
| chr12:102867001
|
A | C | 3 | a0001c0007t0010g0031a0001c0007t0010g0032a0001c0007t0010g0033 | 3 | HG02280.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.442-338T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867001 | ||||||
| chr12:102867041
|
T | C | 75 | a0001c0002t0001g0003a0001c0002t0001g0021a0001c0002t0001g0027others(72): Show | 77 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-378A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867041 | ||||||
| chr12:102867184
|
C | A | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-521G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867184 | ||||||
| chr12:102867184
|
C | T | 11 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-521G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867184 | ||||||
| chr12:102867194
|
G | A | 4 | a0001c0001t0006g0226a0001c0001t0006g0227a0001c0001t0006g0229others(1): Show | 4 | HG02647.hp1 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-531C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867194 | ||||||
| chr12:102867240
|
A | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0067a0001c0001t0001g0159 | 3 | HG00642.hp1 HG01106.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.442-577T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867240 | ||||||
| chr12:102867463
|
G | A | 12 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(9): Show | 12 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-800C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867463 | ||||||
| chr12:102867492
|
A | C | 75 | a0001c0002t0001g0003a0001c0002t0001g0021a0001c0002t0001g0027others(72): Show | 77 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-829T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867492 | ||||||
| chr12:102867498
|
T | C | 1 | a0001c0001t0007g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.442-835A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867498 | ||||||
| chr12:102867801
|
TTTTCTCT others(7): Show |
T | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.442-1152_442-1139d others(16): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867801 | ||||||
| chr12:102867838
|
C | CCT | 71 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(68): Show | 72 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.442-1177_442-1176d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867838 | ||||||
| chr12:102867850
|
T | TATGTATA others(23): Show |
7 | a0001c0003t0001g0048a0001c0003t0001g0049a0001c0003t0001g0050others(4): Show | 7 | HG02523.hp2 HG02559.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-1217_442-1188d others(32): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867850 | ||||||
| chr12:102867850
|
T | TATGTATA others(53): Show |
3 | a0001c0004t0001g0141a0001c0004t0002g0150a0001c0004t0007g0145 | 3 | HG02630.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.442-1247_442-1188d others(62): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867850 | ||||||
| chr12:102867850
|
T | TATGTATA others(83): Show |
11 | a0001c0004t0001g0103a0001c0004t0001g0143a0001c0004t0001g0144others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-1277_442-1188d others(92): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867850 | ||||||
| chr12:102867850
|
TATGTATA others(23): Show |
T | 89 | a0001c0001t0001g0019a0001c0001t0002g0210a0001c0001t0004g0285others(86): Show | 91 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.442-1217_442-1188d others(32): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867850 | ||||||
| chr12:102867850
|
TATGTATA others(53): Show |
T | 1 | a0001c0002t0001g0057 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.442-1247_442-1188d others(62): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867850 | ||||||
| chr12:102867853
|
G | GTATATAC others(25): Show |
2 | a0001c0006t0002g0211a0001c0006t0004g0297 | 2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.442-1222_442-1191d others(34): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867853 | ||||||
| chr12:102867863
|
A | ATATAGAT others(175): Show |
1 | a0001c0009t0013g0240 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.442-1201_442-1200i others(184): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867863 | ||||||
| chr12:102867863
|
A | C | 4 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228others(1): Show | 4 | HG01496.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1200T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867863 | ||||||
| chr12:102867893
|
A | C | 11 | a0001c0006t0001g0213a0001c0008t0001g0133a0001c0008t0001g0134others(8): Show | 11 | HG01496.hp1 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-1230T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867893 | ||||||
| chr12:102867898
|
G | GATGTATA others(23): Show |
11 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0013others(8): Show | 12 | HG00741.hp1 HG01081.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-1236_442-1235i others(32): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867898 | ||||||
| chr12:102867911
|
A | G | 9 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-1248T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867911 | ||||||
| chr12:102867923
|
A | C | 11 | a0001c0006t0001g0213a0001c0008t0001g0133a0001c0008t0001g0134others(8): Show | 11 | HG01496.hp1 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-1260T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867923 | ||||||
| chr12:102867924
|
T | TATAGATG others(23): Show |
2 | a0001c0001t0002g0009a0001c0001t0002g0010 | 2 | HG01167.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.442-1262_442-1261i others(32): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867924 | ||||||
| chr12:102867927
|
AGATG | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0067a0001c0001t0001g0159 | 3 | HG00642.hp1 HG01106.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.442-1268_442-1265d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867927 | ||||||
| chr12:102867941
|
A | G | 13 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(10): Show | 13 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.442-1278T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867941 | ||||||
| chr12:102867950
|
C | CATATATA others(17): Show |
1 | a0001c0009t0013g0240 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.442-1311_442-1288d others(26): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867950 | ||||||
| chr12:102867950
|
C | CATCTATA others(107): Show |
4 | a0001c0009t0005g0236a0001c0009t0005g0238a0001c0009t0013g0239others(1): Show | 4 | HG02257.hp1 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-1288_442-1287i others(116): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867950 | ||||||
| chr12:102867950
|
C | CATCTATA others(107): Show |
2 | a0001c0006t0001g0213a0001c0009t0005g0235 | 2 | HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.442-1288_442-1287i others(116): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867950 | ||||||
| chr12:102867950
|
C | T | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-1287G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867950 | ||||||
| chr12:102867953
|
A | C | 5 | a0001c0003t0003g0291a0001c0008t0001g0133a0001c0008t0001g0134others(2): Show | 5 | HG01496.hp1 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-1290T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867953 | ||||||
| chr12:102867958
|
G | C | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-1295C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867958 | ||||||
| chr12:102867969
|
A | G | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-1306T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867969 | ||||||
| chr12:102867970
|
C | T | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-1307G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867970 | ||||||
| chr12:102867971
|
A | ATGTATAT others(23): Show |
76 | a0001c0001t0001g0026a0001c0001t0001g0044a0001c0001t0001g0045others(73): Show | 77 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-1309_442-1308i others(32): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867971 | ||||||
| chr12:102867971
|
A | ATGTATAT others(23): Show |
2 | a0001c0001t0001g0020a0001c0002t0011g0030 | 2 | HG00738.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.442-1309_442-1308i others(32): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867971 | ||||||
| chr12:102867971
|
A | G | 60 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(57): Show | 61 | HG00099.hp2 HG00558.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.442-1308T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867971 | ||||||
| chr12:102867973
|
G | A | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-1310C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867973 | ||||||
| chr12:102867976
|
T | C | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-1313A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867976 | ||||||
| chr12:102867980
|
T | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 16 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-1317A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867980 | ||||||
| chr12:102867981
|
AGATG | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 16 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-1322_442-1319d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867981 | ||||||
| chr12:102867982
|
G | T | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-1319C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867982 | ||||||
| chr12:102867984
|
T | C | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-1321A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867984 | ||||||
| chr12:102867985
|
G | A | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-1322C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867985 | ||||||
| chr12:102867988
|
TA | T | 59 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(56): Show | 60 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.442-1326delT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867988 | ||||||
| chr12:102867989
|
AT | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(14): Show | 18 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-1327delA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867989 | ||||||
| chr12:102867993
|
C | G | 15 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 16 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-1330G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867993 | ||||||
| chr12:102867993
|
C | T | 1 | a0001c0002t0001g0154 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.442-1330G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867993 | ||||||
| chr12:102867996
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.442-1333C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102867996 | ||||||
| chr12:102868000
|
ATATG | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 16 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-1341_442-1338d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868000 | ||||||
| chr12:102868001
|
T | G | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.442-1338A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868001 | ||||||
| chr12:102868001
|
T | TACATATA others(15): Show |
1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-1339_442-1338i others(24): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868001 | ||||||
| chr12:102868002
|
A | ACATCTAT others(5): Show |
1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1340_442-1339i others(14): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868002 | ||||||
| chr12:102868004
|
G | A | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1341C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868004 | ||||||
| chr12:102868009
|
T | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 16 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-1346A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868009 | ||||||
| chr12:102868011
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 16 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-1348G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868011 | ||||||
| chr12:102868012
|
A | G | 15 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 16 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-1349T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868012 | ||||||
| chr12:102868015
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.442-1352A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868015 | ||||||
| chr12:102868016
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.442-1353T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868016 | ||||||
| chr12:102868018
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.442-1355T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868018 | ||||||
| chr12:102868019
|
C | T | 2 | a0001c0001t0001g0086a0001c0004t0026g0304 | 2 | HG01175.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.442-1356G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868019 | ||||||
| chr12:102868027
|
C | G | 17 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(14): Show | 18 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-1364G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868027 | ||||||
| chr12:102868032
|
A | G | 14 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-1369T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868032 | ||||||
| chr12:102868037
|
C | T | 16 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 17 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.442-1374G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868037 | ||||||
| chr12:102868038
|
ACCTATAT others(43): Show |
A | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.442-1425_442-1376d others(52): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868038 | ||||||
| chr12:102868039
|
C | G | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-1376G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868039 | ||||||
| chr12:102868039
|
C | T | 3 | a0001c0006t0002g0211a0001c0006t0004g0297a0001c0008t0018g0215 | 3 | HG01496.hp1 HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.442-1376G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868039 | ||||||
| chr12:102868040
|
C | A | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-1377G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868040 | ||||||
| chr12:102868040
|
C | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 17 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.442-1377G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868040 | ||||||
| chr12:102868042
|
A | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 17 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.442-1379T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868042 | ||||||
| chr12:102868048
|
A | ATG | 75 | a0001c0002t0001g0003a0001c0002t0001g0021a0001c0002t0001g0027others(72): Show | 77 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-1387_442-1386d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868048 | ||||||
| chr12:102868049
|
T | C | 148 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(145): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.442-1386A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868049 | ||||||
| chr12:102868049
|
T | G | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1386A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868049 | ||||||
| chr12:102868050
|
G | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0041others(16): Show | 20 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.442-1387C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868050 | ||||||
| chr12:102868051
|
T | G | 15 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 16 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-1388A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868051 | ||||||
| chr12:102868051
|
TATATATA others(5): Show |
T | 2 | a0001c0006t0002g0211a0001c0006t0004g0297 | 2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.442-1400_442-1389d others(14): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868051 | ||||||
| chr12:102868052
|
A | G | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1389T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868052 | ||||||
| chr12:102868054
|
A | G | 15 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 16 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-1391T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868054 | ||||||
| chr12:102868058
|
A | AT | 3 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042 | 4 | HG01069.hp1 HG01243.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1396dupA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868058 | ||||||
| chr12:102868058
|
A | G | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-1395T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868058 | ||||||
| chr12:102868058
|
A | T | 12 | a0001c0001t0002g0164a0001c0001t0002g0198a0001c0001t0002g0216others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-1395T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868058 | ||||||
| chr12:102868059
|
T | C | 6 | a0001c0001t0001g0018a0001c0001t0002g0013a0001c0001t0002g0014others(3): Show | 6 | HG02258.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-1396A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868059 | ||||||
| chr12:102868061
|
C | T | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-1398G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868061 | ||||||
| chr12:102868062
|
ACATATAT others(19): Show |
A | 15 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 16 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-1425_442-1400d others(28): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868062 | ||||||
| chr12:102868063
|
C | T | 2 | a0001c0004t0026g0304a0001c0008t0018g0215 | 2 | HG01175.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.442-1400G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868063 | ||||||
| chr12:102868064
|
A | G | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1401T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868064 | ||||||
| chr12:102868065
|
T | C | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-1402A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868065 | ||||||
| chr12:102868070
|
A | G | 14 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-1407T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868070 | ||||||
| chr12:102868071
|
T | C | 10 | a0001c0006t0001g0213a0001c0008t0001g0133a0001c0008t0001g0134others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-1408A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868071 | ||||||
| chr12:102868073
|
C | G | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1410G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868073 | ||||||
| chr12:102868076
|
A | G | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1413T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868076 | ||||||
| chr12:102868078
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0008t0001g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.442-1425_442-1416d others(12): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868078 | ||||||
| chr12:102868080
|
G | A | 9 | a0001c0004t0026g0304a0001c0006t0001g0213a0001c0008t0018g0215others(6): Show | 9 | HG01175.hp2 HG01496.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-1417C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868080 | ||||||
| chr12:102868081
|
T | C | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-1418A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868081 | ||||||
| chr12:102868081
|
T | TAC | 4 | a0001c0009t0005g0235a0001c0009t0005g0236a0001c0009t0005g0238others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1419_442-1418i others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868081 | ||||||
| chr12:102868082
|
G | A | 9 | a0001c0004t0026g0304a0001c0006t0001g0213a0001c0008t0018g0215others(6): Show | 9 | HG01175.hp2 HG01496.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-1419C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868082 | ||||||
| chr12:102868083
|
T | C | 2 | a0001c0006t0001g0213a0003c0013t0005g0237 | 2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.442-1420A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868083 | ||||||
| chr12:102868084
|
G | A | 7 | a0001c0006t0001g0213a0001c0009t0005g0235a0001c0009t0005g0236others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-1421C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868084 | ||||||
| chr12:102868084
|
G | GTATATAC others(3): Show |
1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-1422_442-1421i others(12): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868084 | ||||||
| chr12:102868084
|
GTGTGTAT others(95): Show |
G | 2 | a0001c0001t0003g0233a0001c0002t0011g0030 | 2 | HG00642.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.442-1523_442-1422d others(2): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868084 | ||||||
| chr12:102868084
|
GTGTGTAT others(97): Show |
G | 59 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(56): Show | 60 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.442-1525_442-1422d others(2): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868084 | ||||||
| chr12:102868084
|
GTGTGTAT others(99): Show |
G | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.442-1527_442-1422d others(2): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868084 | ||||||
| chr12:102868086
|
G | A | 8 | a0001c0004t0026g0304a0001c0006t0001g0213a0001c0008t0018g0215others(5): Show | 8 | HG01175.hp2 HG01496.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-1423C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868086 | ||||||
| chr12:102868086
|
GTGTATAT others(95): Show |
G | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-1525_442-1424d others(2): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868086 | ||||||
| chr12:102868086
|
GTGTATAT others(99): Show |
G | 14 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-1529_442-1424d others(2): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868086 | ||||||
| chr12:102868088
|
G | A | 6 | a0001c0004t0026g0304a0001c0006t0001g0213a0001c0008t0001g0134others(3): Show | 6 | HG01175.hp2 HG01496.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-1425C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868088 | ||||||
| chr12:102868088
|
GTATATAT others(43): Show |
G | 1 | a0001c0003t0005g0260 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.442-1475_442-1426d others(52): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868088 | ||||||
| chr12:102868088
|
GTATATAT others(89): Show |
G | 1 | a0001c0001t0002g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.442-1521_442-1426d others(98): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868088 | ||||||
| chr12:102868088
|
GTATATAT others(91): Show |
G | 58 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(55): Show | 59 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.442-1523_442-1426d others(100): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868088 | ||||||
| chr12:102868088
|
GTATATAT others(93): Show |
G | 2 | a0001c0006t0002g0211a0001c0006t0004g0297 | 2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.442-1525_442-1426d others(102): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868088 | ||||||
| chr12:102868090
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(94): Show | 100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.442-1427T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868090 | ||||||
| chr12:102868091
|
T | C | 2 | a0001c0008t0001g0134a0001c0008t0001g0228 | 2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.442-1428A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868091 | ||||||
| chr12:102868092
|
A | G | 3 | a0001c0006t0001g0213a0001c0008t0018g0215a0003c0013t0005g0237 | 3 | HG01496.hp1 HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.442-1429T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868092 | ||||||
| chr12:102868093
|
T | C | 1 | a0001c0008t0001g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.442-1430A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868093 | ||||||
| chr12:102868094
|
A | G | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-1431T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868094 | ||||||
| chr12:102868098
|
A | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(15): Show | 19 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.442-1435T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868098 | ||||||
| chr12:102868099
|
T | C | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1436A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868099 | ||||||
| chr12:102868100
|
A | G | 3 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228 | 3 | HG02630.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.442-1437T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868100 | ||||||
| chr12:102868102
|
A | G | 1 | a0001c0008t0001g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.442-1439T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868102 | ||||||
| chr12:102868105
|
C | T | 4 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228others(1): Show | 4 | HG01496.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1442G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868105 | ||||||
| chr12:102868107
|
C | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(16): Show | 20 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.442-1444G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868107 | ||||||
| chr12:102868113
|
T | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 17 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.442-1450A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868113 | ||||||
| chr12:102868114
|
A | G | 2 | a0001c0003t0001g0204a0001c0003t0003g0258 | 2 | NA18963.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.442-1451T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868114 | ||||||
| chr12:102868117
|
C | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(14): Show | 18 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-1454G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868117 | ||||||
| chr12:102868119
|
T | C | 3 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228 | 3 | HG02630.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.442-1456A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868119 | ||||||
| chr12:102868121
|
T | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(14): Show | 18 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-1458A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868121 | ||||||
| chr12:102868122
|
A | ATG | 4 | a0001c0003t0003g0284a0001c0003t0003g0288a0001c0003t0003g0289others(1): Show | 4 | HG00609.hp1 HG00673.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-1461_442-1460d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868122 | ||||||
| chr12:102868123
|
T | C | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1460A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868123 | ||||||
| chr12:102868124
|
G | A | 3 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228 | 3 | HG02630.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.442-1461C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868124 | ||||||
| chr12:102868124
|
G | C | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1461C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868124 | ||||||
| chr12:102868126
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(14): Show | 18 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-1463C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868126 | ||||||
| chr12:102868126
|
G | GTA | 13 | a0001c0003t0001g0049a0001c0003t0001g0050a0001c0003t0001g0107others(10): Show | 13 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-1465_442-1464d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868126 | ||||||
| chr12:102868126
|
GTA | G | 5 | a0001c0003t0001g0204a0001c0003t0003g0006a0001c0003t0003g0256others(2): Show | 6 | HG03491.hp1 HG03492.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-1465_442-1464d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868126 | ||||||
| chr12:102868126
|
GTATATAT others(5): Show |
G | 7 | a0001c0006t0001g0213a0001c0009t0005g0235a0001c0009t0005g0236others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-1475_442-1464d others(14): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868126 | ||||||
| chr12:102868126
|
GTATATAT others(45): Show |
G | 14 | a0001c0003t0003g0291a0001c0004t0001g0103a0001c0004t0001g0141others(11): Show | 14 | HG01109.hp1 HG01243.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.442-1515_442-1464d others(54): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868126 | ||||||
| chr12:102868126
|
GTATATAT others(47): Show |
G | 1 | a0001c0004t0008g0300 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.442-1517_442-1464d others(56): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868126 | ||||||
| chr12:102868128
|
A | G | 1 | a0001c0003t0003g0287 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.442-1465T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868128 | ||||||
| chr12:102868128
|
ATATATAT others(41): Show |
A | 61 | a0001c0002t0001g0003a0001c0002t0001g0021a0001c0002t0001g0027others(58): Show | 63 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.442-1513_442-1466d others(50): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868128 | ||||||
| chr12:102868130
|
ATATATAT others(39): Show |
A | 10 | a0001c0002t0001g0051a0001c0002t0001g0060a0001c0002t0001g0063others(7): Show | 10 | HG00408.hp1 HG01257.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-1513_442-1468d others(48): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868130 | ||||||
| chr12:102868131
|
T | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 17 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.442-1468A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868131 | ||||||
| chr12:102868132
|
ATATATAT others(37): Show |
A | 3 | a0001c0002t0001g0059a0001c0002t0001g0079a0001c0002t0001g0095 | 3 | HG01516.hp1 HG03654.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.442-1513_442-1470d others(46): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868132 | ||||||
| chr12:102868133
|
T | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(14): Show | 18 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-1470A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868133 | ||||||
| chr12:102868134
|
A | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 17 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.442-1471T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868134 | ||||||
| chr12:102868134
|
A | G | 2 | a0001c0004t0026g0304a0001c0008t0018g0215 | 2 | HG01175.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.442-1471T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868134 | ||||||
| chr12:102868136
|
A | G | 4 | a0001c0004t0026g0304a0001c0008t0001g0133a0001c0008t0001g0134others(1): Show | 4 | HG01175.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1473T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868136 | ||||||
| chr12:102868136
|
ATATATAT others(33): Show |
A | 1 | a0001c0002t0001g0094 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.442-1513_442-1474d others(42): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868136 | ||||||
| chr12:102868138
|
A | G | 4 | a0001c0004t0026g0304a0001c0008t0001g0133a0001c0008t0001g0134others(1): Show | 4 | HG01175.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1475T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868138 | ||||||
| chr12:102868143
|
T | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 17 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.442-1480A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868143 | ||||||
| chr12:102868144
|
A | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 17 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.442-1481T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868144 | ||||||
| chr12:102868145
|
T | C | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1482A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868145 | ||||||
| chr12:102868147
|
T | C | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1484A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868147 | ||||||
| chr12:102868155
|
C | T | 1 | a0001c0008t0001g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.442-1492G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868155 | ||||||
| chr12:102868159
|
T | C | 1 | a0001c0003t0001g0115 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.442-1496A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868159 | ||||||
| chr12:102868167
|
C | T | 3 | a0001c0003t0003g0259a0001c0003t0003g0280a0004c0016t0003g0281 | 3 | HG00735.hp2 HG02293.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.442-1504G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868167 | ||||||
| chr12:102868172
|
A | ATG | 5 | a0001c0009t0005g0235a0001c0009t0005g0236a0001c0009t0005g0238others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-1511_442-1510d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868172 | ||||||
| chr12:102868176
|
G | GTA | 12 | a0001c0003t0003g0263a0001c0003t0003g0270a0001c0003t0014g0279others(9): Show | 12 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-1515_442-1514d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868176 | ||||||
| chr12:102868176
|
GTATA | G | 12 | a0001c0001t0002g0164a0001c0001t0002g0198a0001c0001t0002g0216others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-1517_442-1514d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868176 | ||||||
| chr12:102868176
|
GTATATA | G | 3 | a0001c0008t0001g0133a0001c0008t0001g0134a0001c0008t0001g0228 | 3 | HG02630.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.442-1519_442-1514d others(8): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868176 | ||||||
| chr12:102868176
|
GTATATAT others(3): Show |
G | 4 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 5 | HG01069.hp1 HG01243.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-1523_442-1514d others(12): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868176 | ||||||
| chr12:102868178
|
A | G | 1 | a0001c0009t0013g0240 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.442-1515T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868178 | ||||||
| chr12:102868180
|
A | G | 10 | a0001c0004t0001g0103a0001c0004t0001g0141a0001c0004t0001g0143others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-1517T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868180 | ||||||
| chr12:102868182
|
A | G | 12 | a0001c0001t0002g0164a0001c0001t0002g0198a0001c0001t0002g0216others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-1519T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868182 | ||||||
| chr12:102868184
|
A | G | 12 | a0001c0001t0002g0164a0001c0001t0002g0198a0001c0001t0002g0216others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-1521T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868184 | ||||||
| chr12:102868186
|
A | G | 12 | a0001c0001t0002g0164a0001c0001t0002g0198a0001c0001t0002g0216others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-1523T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868186 | ||||||
| chr12:102868188
|
A | ATATACAC others(19): Show |
1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1526_442-1525i others(28): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868188 | ||||||
| chr12:102868188
|
A | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 8 | HG01069.hp1 HG01243.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-1525T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868188 | ||||||
| chr12:102868234
|
A | G | 1 | a0001c0003t0003g0269 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.442-1571T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868234 | ||||||
| chr12:102868255
|
T | A | 11 | a0001c0006t0001g0213a0001c0008t0001g0133a0001c0008t0001g0134others(8): Show | 11 | HG01496.hp1 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-1592A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868255 | ||||||
| chr12:102868313
|
C | A | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1650G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868313 | ||||||
| chr12:102868435
|
A | AT | 16 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(13): Show | 16 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-1773dupA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868435 | ||||||
| chr12:102868495
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.442-1832C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868495 | ||||||
| chr12:102868508
|
G | A | 1 | a0001c0001t0004g0262 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.442-1845C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868508 | ||||||
| chr12:102868663
|
TA | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(148): Show | 154 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.442-2001delT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868663 | ||||||
| chr12:102868663
|
TAA | T | 13 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-2002_442-2001d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868663 | ||||||
| chr12:102868759
|
T | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(64): Show | 69 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.442-2096A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868759 | ||||||
| chr12:102868836
|
C | T | 1 | a0001c0010t0001g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.442-2173G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868836 | ||||||
| chr12:102868911
|
T | C | 1 | a0001c0002t0001g0090 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.442-2248A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102868911 | ||||||
| chr12:102869008
|
A | G | 8 | a0001c0006t0001g0213a0001c0008t0018g0215a0001c0009t0005g0235others(5): Show | 8 | HG01496.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-2345T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102869008 | ||||||
| chr12:102869126
|
C | T | 71 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(68): Show | 72 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.442-2463G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102869126 | ||||||
| chr12:102869367
|
A | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(138): Show | 144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.442-2704T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102869367 | ||||||
| chr12:102869482
|
C | T | 6 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-2819G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102869482 | ||||||
| chr12:102869651
|
C | T | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-2988G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102869651 | ||||||
| chr12:102869705
|
A | C | 1 | a0001c0001t0006g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-3042T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102869705 | ||||||
| chr12:102869706
|
G | A | 15 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(12): Show | 15 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.442-3043C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102869706 | ||||||
| chr12:102869756
|
C | T | 4 | a0001c0003t0003g0269a0002c0005t0003g0247a0002c0005t0003g0250others(1): Show | 4 | NA18983.hp2 NA18985.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-3093G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102869756 | ||||||
| chr12:102869799
|
C | T | 60 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(57): Show | 61 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.442-3136G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102869799 | ||||||
| chr12:102869803
|
C | A | 8 | a0001c0006t0001g0213a0001c0008t0018g0215a0001c0009t0005g0235others(5): Show | 8 | HG01496.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-3140G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102869803 | ||||||
| chr12:102869803
|
C | T | 83 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(80): Show | 85 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.442-3140G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102869803 | ||||||
| chr12:102869804
|
G | A | 66 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(63): Show | 67 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.442-3141C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102869804 | ||||||
| chr12:102869824
|
C | T | 85 | a0001c0001t0001g0128a0001c0001t0002g0008a0001c0001t0002g0009others(82): Show | 87 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.442-3161G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102869824 | ||||||
| chr12:102870141
|
G | T | 6 | a0001c0001t0004g0295a0001c0001t0004g0296a0001c0006t0002g0211others(3): Show | 6 | HG02258.hp1 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-3478C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102870141 | ||||||
| chr12:102870341
|
A | T | 235 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(232): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.442-3678T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102870341 | ||||||
| chr12:102870461
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.442-3798C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102870461 | ||||||
| chr12:102870508
|
A | G | 1 | a0001c0010t0001g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.442-3845T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102870508 | ||||||
| chr12:102870561
|
A | G | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-3898T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102870561 | ||||||
| chr12:102870834
|
G | T | 1 | a0001c0007t0002g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.442-4171C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102870834 | ||||||
| chr12:102870873
|
T | C | 1 | a0001c0002t0001g0097 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.442-4210A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102870873 | ||||||
| chr12:102870887
|
T | G | 11 | a0001c0004t0001g0103a0001c0004t0001g0140a0001c0004t0001g0141others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-4224A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102870887 | ||||||
| chr12:102871087
|
T | C | 1 | a0001c0002t0001g0158 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.442-4424A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871087 | ||||||
| chr12:102871126
|
T | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(232): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.442-4463A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871126 | ||||||
| chr12:102871135
|
A | G | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.442-4472T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871135 | ||||||
| chr12:102871325
|
T | A | 1 | a0001c0001t0002g0004 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-4662A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871325 | ||||||
| chr12:102871373
|
G | C | 4 | a0001c0009t0005g0235a0001c0009t0005g0236a0001c0009t0005g0238others(1): Show | 4 | HG02257.hp1 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-4710C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871373 | ||||||
| chr12:102871421
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0067a0001c0001t0001g0159 | 3 | HG00642.hp1 HG01106.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.442-4758C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871421 | ||||||
| chr12:102871511
|
G | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 153 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.442-4848C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871511 | ||||||
| chr12:102871561
|
T | C | 68 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(65): Show | 69 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.442-4898A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871561 | ||||||
| chr12:102871642
|
G | T | 3 | a0001c0003t0003g0006a0001c0003t0003g0256a0001c0003t0003g0264 | 4 | HG01168.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-4979C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871642 | ||||||
| chr12:102871877
|
A | G | 236 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(233): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.442-5214T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871877 | ||||||
| chr12:102871886
|
C | T | 10 | a0001c0001t0011g0132a0001c0006t0001g0213a0001c0006t0016g0163others(7): Show | 10 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-5223G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871886 | ||||||
| chr12:102871931
|
AAAAAAAA others(17): Show |
A | 2 | a0001c0001t0001g0047a0001c0002t0011g0089 | 2 | HG03654.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.442-5292_442-5269d others(26): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871931 | ||||||
| chr12:102871931
|
AAAAAAAA others(19): Show |
A | 1 | a0001c0002t0001g0182 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.442-5294_442-5269d others(28): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871931 | ||||||
| chr12:102871931
|
AAAAAAAA others(21): Show |
A | 4 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0124others(1): Show | 4 | NA18954.hp2 NA18982.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-5296_442-5269d others(30): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871931 | ||||||
| chr12:102871932
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0002g0004 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-5288_442-5270d others(21): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871932 | ||||||
| chr12:102871932
|
AAAAAAAA others(14): Show |
A | 3 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0011t0002g0069 | 3 | HG00741.hp1 HG01081.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.442-5290_442-5270d others(23): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871932 | ||||||
| chr12:102871932
|
AAAAAAAA others(16): Show |
A | 2 | a0001c0001t0001g0199a0001c0001t0002g0161 | 2 | HG02004.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.442-5292_442-5270d others(25): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871932 | ||||||
| chr12:102871932
|
AAAAAAAA others(18): Show |
A | 5 | a0001c0002t0001g0061a0001c0002t0001g0064a0001c0002t0001g0065others(2): Show | 5 | NA18992.hp2 NA18999.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-5294_442-5270d others(27): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871932 | ||||||
| chr12:102871933
|
AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0001g0206 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.442-5292_442-5271d others(24): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871933 | ||||||
| chr12:102871933
|
AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0001g0020 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.442-5294_442-5271d others(26): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871933 | ||||||
| chr12:102871933
|
AAAAAAAA others(19): Show |
A | 2 | a0001c0002t0001g0073a0001c0002t0001g0185 | 2 | NA18951.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.442-5296_442-5271d others(28): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871933 | ||||||
| chr12:102871933
|
AAAAAAAA others(21): Show |
A | 47 | a0001c0002t0001g0003a0001c0002t0001g0021a0001c0002t0001g0027others(44): Show | 48 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.442-5298_442-5271d others(30): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871933 | ||||||
| chr12:102871934
|
A | T | 1 | a0001c0001t0002g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.442-5271T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871934 | ||||||
| chr12:102871934
|
AAAAAAAA others(12): Show |
A | 6 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167others(3): Show | 6 | HG01928.hp1 HG01952.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-5290_442-5272d others(21): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871934 | ||||||
| chr12:102871934
|
AAAAAAAA others(16): Show |
A | 32 | a0001c0001t0001g0053a0001c0001t0001g0184a0001c0001t0001g0202others(29): Show | 33 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.442-5294_442-5272d others(25): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871934 | ||||||
| chr12:102871934
|
AAAAAAAA others(18): Show |
A | 8 | a0001c0001t0002g0200a0001c0002t0001g0158a0001c0002t0001g0209others(5): Show | 8 | HG02451.hp1 HG02486.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-5296_442-5272d others(27): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871934 | ||||||
| chr12:102871934
|
AAAAAAAA others(20): Show |
A | 2 | a0001c0002t0001g0074a0001c0002t0001g0084 | 2 | HG01496.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.442-5298_442-5272d others(29): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871934 | ||||||
| chr12:102871935
|
AAAAAAAA others(15): Show |
A | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0138others(3): Show | 6 | HG01074.hp1 HG01255.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-5294_442-5273d others(24): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871935 | ||||||
| chr12:102871935
|
AAAAAAAA others(17): Show |
A | 9 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0041others(6): Show | 10 | HG01069.hp1 HG01243.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-5296_442-5273d others(26): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871935 | ||||||
| chr12:102871935
|
AAAAAAAA others(21): Show |
A | 10 | a0001c0002t0001g0038a0001c0002t0001g0058a0001c0002t0001g0059others(7): Show | 11 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-5300_442-5273d others(30): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871935 | ||||||
| chr12:102871936
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0002g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.442-5288_442-5274d others(17): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871936 | ||||||
| chr12:102871936
|
AAAAAAAA others(12): Show |
A | 2 | a0001c0007t0010g0031a0001c0007t0010g0033 | 2 | HG02280.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.442-5292_442-5274d others(21): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871936 | ||||||
| chr12:102871936
|
AAAAAAAA others(14): Show |
A | 3 | a0001c0001t0002g0014a0001c0001t0002g0164a0001c0006t0016g0163 | 3 | HG01981.hp1 HG02976.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.442-5294_442-5274d others(23): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871936 | ||||||
| chr12:102871936
|
AAAAAAAA others(16): Show |
A | 5 | a0001c0001t0001g0179a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01358.hp1 HG03579.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-5296_442-5274d others(25): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871936 | ||||||
| chr12:102871936
|
AAAAAAAA others(20): Show |
A | 4 | a0001c0001t0003g0233a0001c0001t0025g0234a0001c0008t0023g0242others(1): Show | 4 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-5300_442-5274d others(29): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871936 | ||||||
| chr12:102871937
|
A | T | 2 | a0001c0006t0004g0292a0001c0006t0004g0293 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.442-5274T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871937 | ||||||
| chr12:102871937
|
AAAAAAAA others(15): Show |
A | 8 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0112others(5): Show | 8 | HG00140.hp2 HG00642.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-5296_442-5275d others(24): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871937 | ||||||
| chr12:102871937
|
AAAAAAAA others(17): Show |
A | 29 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(26): Show | 29 | HG00099.hp2 HG00558.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.442-5298_442-5275d others(26): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871937 | ||||||
| chr12:102871937
|
AAAAAAAA others(19): Show |
A | 1 | a0001c0001t0004g0232 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.442-5300_442-5275d others(28): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871937 | ||||||
| chr12:102871937
|
AAAAAAAA others(21): Show |
A | 1 | a0001c0002t0003g0231 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.442-5302_442-5275d others(30): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871937 | ||||||
| chr12:102871938
|
AAAAAAAA others(14): Show |
A | 2 | a0001c0001t0001g0067a0001c0001t0001g0071 | 2 | HG01106.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.442-5296_442-5276d others(23): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871938 | ||||||
| chr12:102871938
|
AAAAAAAA others(16): Show |
A | 2 | a0001c0001t0001g0189a0001c0001t0002g0008 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.442-5298_442-5276d others(25): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871938 | ||||||
| chr12:102871938
|
AAAAAAAA others(18): Show |
A | 2 | a0001c0001t0001g0072a0001c0001t0001g0220 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.442-5300_442-5276d others(27): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871938 | ||||||
| chr12:102871938
|
AAAAAAAA others(22): Show |
A | 2 | a0001c0004t0001g0144a0005c0017t0001g0142 | 2 | HG01109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.442-5304_442-5276d others(31): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871938 | ||||||
| chr12:102871939
|
A | T | 6 | a0001c0001t0004g0285a0001c0001t0004g0286a0001c0001t0004g0295others(3): Show | 6 | HG02258.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-5276T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871939 | ||||||
| chr12:102871939
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0001g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.442-5296_442-5277d others(22): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871939 | ||||||
| chr12:102871939
|
AAAAAAAA others(15): Show |
A | 5 | a0001c0001t0001g0054a0001c0001t0001g0104a0001c0001t0001g0120others(2): Show | 5 | HG02922.hp1 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-5298_442-5277d others(24): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871939 | ||||||
| chr12:102871939
|
AAAAAAAA others(17): Show |
A | 7 | a0001c0001t0001g0070a0001c0001t0002g0188a0001c0001t0002g0216others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-5300_442-5277d others(26): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871939 | ||||||
| chr12:102871939
|
AAAAAAAA others(19): Show |
A | 6 | a0001c0004t0001g0141a0001c0004t0001g0147a0001c0004t0001g0149others(3): Show | 6 | HG01243.hp1 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-5302_442-5277d others(28): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871939 | ||||||
| chr12:102871939
|
AAAAAAAA others(21): Show |
A | 2 | a0001c0004t0001g0103a0001c0004t0001g0143 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-5304_442-5277d others(30): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871939 | ||||||
| chr12:102871940
|
AAAAAAAA others(14): Show |
A | 1 | a0001c0001t0007g0017 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.442-5298_442-5278d others(23): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871940 | ||||||
| chr12:102871940
|
AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0009g0299 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.442-5302_442-5278d others(27): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871940 | ||||||
| chr12:102871941
|
A | T | 8 | a0001c0001t0002g0155a0001c0001t0004g0285a0001c0001t0004g0286others(5): Show | 8 | HG02258.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-5278T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871941 | ||||||
| chr12:102871941
|
AAAAAAAA others(15): Show |
A | 2 | a0001c0001t0001g0091a0001c0001t0002g0013 | 2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.442-5300_442-5279d others(24): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871941 | ||||||
| chr12:102871943
|
A | T | 9 | a0001c0001t0002g0155a0001c0001t0004g0285a0001c0001t0004g0286others(6): Show | 9 | HG02258.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-5280T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871943 | ||||||
| chr12:102871944
|
AAAAAAAT others(8): Show |
A | 1 | a0001c0001t0001g0221 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.442-5296_442-5282d others(17): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871944 | ||||||
| chr12:102871945
|
A | T | 10 | a0001c0001t0002g0155a0001c0001t0002g0210a0001c0001t0004g0285others(7): Show | 10 | HG02258.hp1 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-5282T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871945 | ||||||
| chr12:102871945
|
AAAAAATA others(7): Show |
A | 6 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | HG02145.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-5296_442-5283d others(16): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871945 | ||||||
| chr12:102871947
|
A | T | 10 | a0001c0001t0002g0155a0001c0001t0002g0210a0001c0001t0004g0285others(7): Show | 10 | HG02258.hp1 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-5284T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871947 | ||||||
| chr12:102871949
|
A | AATATATA others(5): Show |
1 | a0001c0009t0005g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.442-5298_442-5287d others(14): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871949 | ||||||
| chr12:102871949
|
A | T | 12 | a0001c0001t0002g0155a0001c0001t0002g0210a0001c0001t0004g0285others(9): Show | 12 | HG02258.hp1 HG02486.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-5286T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871949 | ||||||
| chr12:102871949
|
AATAT | A | 9 | a0001c0003t0001g0115a0001c0003t0003g0244a0001c0003t0003g0257others(6): Show | 9 | HG00408.hp2 HG00597.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-5290_442-5287d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871949 | ||||||
| chr12:102871949
|
AATATAT | A | 10 | a0001c0003t0003g0265a0001c0003t0003g0266a0001c0003t0003g0289others(7): Show | 10 | HG00609.hp1 HG01516.hp2 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-5292_442-5287d others(8): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871949 | ||||||
| chr12:102871950
|
ATATAT | A | 21 | a0001c0003t0001g0048a0001c0003t0001g0049a0001c0003t0001g0050others(18): Show | 22 | HG00735.hp2 HG01168.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.442-5292_442-5288d others(7): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871950 | ||||||
| chr12:102871951
|
T | A | 1 | a0001c0006t0001g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.442-5288A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871951 | ||||||
| chr12:102871953
|
T | A | 1 | a0001c0001t0011g0132 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.442-5290A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871953 | ||||||
| chr12:102871955
|
T | A | 10 | a0001c0001t0002g0004a0001c0001t0011g0132a0001c0003t0001g0115others(7): Show | 11 | HG00408.hp2 HG00597.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-5292A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871955 | ||||||
| chr12:102871957
|
T | A | 11 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0011g0132others(8): Show | 11 | HG00609.hp1 HG00673.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-5294A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102871957 | ||||||
| chr12:102872043
|
T | C | 1 | a0001c0004t0007g0145 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.442-5380A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102872043 | ||||||
| chr12:102872108
|
C | T | 75 | a0001c0002t0001g0003a0001c0002t0001g0021a0001c0002t0001g0027others(72): Show | 77 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.441+5354G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102872108 | ||||||
| chr12:102872121
|
G | A | 75 | a0001c0002t0001g0003a0001c0002t0001g0021a0001c0002t0001g0027others(72): Show | 77 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.441+5341C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102872121 | ||||||
| chr12:102872248
|
C | A | 1 | a0001c0001t0002g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.441+5214G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102872248 | ||||||
| chr12:102872401
|
T | C | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.441+5061A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102872401 | ||||||
| chr12:102872510
|
G | C | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.441+4952C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102872510 | ||||||
| chr12:102872528
|
C | T | 1 | a0001c0003t0005g0260 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.441+4934G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102872528 | ||||||
| chr12:102872602
|
TG | T | 6 | a0001c0001t0001g0018a0001c0001t0002g0013a0001c0001t0002g0014others(3): Show | 6 | HG02258.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+4859delC | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102872602 | ||||||
| chr12:102872872
|
G | T | 1 | a0001c0001t0011g0132 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.441+4590C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102872872 | ||||||
| chr12:102873006
|
T | C | 1 | a0001c0004t0008g0303 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.441+4456A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873006 | ||||||
| chr12:102873061
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.441+4401G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873061 | ||||||
| chr12:102873092
|
C | A | 2 | a0001c0001t0002g0168a0001c0001t0002g0171 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.441+4370G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873092 | ||||||
| chr12:102873225
|
T | A | 10 | a0001c0001t0011g0132a0001c0006t0001g0213a0001c0006t0016g0163others(7): Show | 10 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+4237A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873225 | ||||||
| chr12:102873419
|
G | C | 94 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(91): Show | 96 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.441+4043C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873419 | ||||||
| chr12:102873579
|
C | T | 11 | a0001c0004t0001g0103a0001c0004t0001g0140a0001c0004t0001g0141others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+3883G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873579 | ||||||
| chr12:102873687
|
A | G | 29 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(26): Show | 29 | HG00099.hp2 HG00558.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.441+3775T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873687 | ||||||
| chr12:102873706
|
C | T | 2 | a0001c0008t0023g0242a0001c0008t0024g0241 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.441+3756G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873706 | ||||||
| chr12:102873765
|
A | G | 9 | a0001c0001t0011g0132a0001c0006t0001g0213a0001c0008t0018g0215others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+3697T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873765 | ||||||
| chr12:102873765
|
A | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 5 | HG01074.hp2 HG01099.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+3697T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873765 | ||||||
| chr12:102873834
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.441+3628G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873834 | ||||||
| chr12:102873931
|
A | G | 6 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+3531T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873931 | ||||||
| chr12:102873938
|
C | T | 2 | a0001c0003t0005g0260a0001c0014t0003g0261 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.441+3524G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873938 | ||||||
| chr12:102873992
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(62): Show | 67 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.441+3470C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102873992 | ||||||
| chr12:102874216
|
A | C | 1 | a0001c0002t0001g0181 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.441+3246T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102874216 | ||||||
| chr12:102874225
|
G | A | 2 | a0001c0008t0023g0242a0001c0008t0024g0241 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.441+3237C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102874225 | ||||||
| chr12:102874594
|
A | C | 1 | a0001c0012t0002g0214 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.441+2868T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102874594 | ||||||
| chr12:102874698
|
G | A | 2 | a0001c0008t0001g0133a0001c0008t0001g0134 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.441+2764C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102874698 | ||||||
| chr12:102874908
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(61): Show | 66 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.441+2554G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102874908 | ||||||
| chr12:102874943
|
C | T | 9 | a0001c0001t0011g0132a0001c0006t0001g0213a0001c0008t0018g0215others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+2519G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102874943 | ||||||
| chr12:102874970
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.441+2492G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102874970 | ||||||
| chr12:102875049
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.441+2413G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875049 | ||||||
| chr12:102875371
|
G | A | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.441+2091C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875371 | ||||||
| chr12:102875375
|
C | T | 1 | a0001c0001t0002g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.441+2087G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875375 | ||||||
| chr12:102875380
|
G | A | 1 | a0001c0003t0003g0245 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.441+2082C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875380 | ||||||
| chr12:102875434
|
C | T | 1 | a0001c0002t0001g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.441+2028G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875434 | ||||||
| chr12:102875565
|
G | A | 2 | a0001c0001t0012g0146a0001c0001t0012g0190 | 2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.441+1897C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875565 | ||||||
| chr12:102875610
|
G | A | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.441+1852C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875610 | ||||||
| chr12:102875621
|
T | A | 16 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(13): Show | 16 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.441+1841A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875621 | ||||||
| chr12:102875630
|
T | C | 15 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(12): Show | 15 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.441+1832A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875630 | ||||||
| chr12:102875638
|
A | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(62): Show | 67 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.441+1824T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875638 | ||||||
| chr12:102875649
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.441+1813C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875649 | ||||||
| chr12:102875684
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.441+1778C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875684 | ||||||
| chr12:102875708
|
A | G | 1 | a0001c0001t0009g0305 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.441+1754T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875708 | ||||||
| chr12:102875840
|
C | T | 9 | a0001c0001t0011g0132a0001c0006t0001g0213a0001c0008t0018g0215others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+1622G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875840 | ||||||
| chr12:102875855
|
G | A | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+1607C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875855 | ||||||
| chr12:102875885
|
CACAA | C | 16 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(13): Show | 16 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.441+1573_441+1576d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875885 | ||||||
| chr12:102875926
|
C | CAT | 71 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(68): Show | 72 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.441+1534_441+1535d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875926 | ||||||
| chr12:102875954
|
C | CAGAG | 234 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(231): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.441+1504_441+1507d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102875954 | ||||||
| chr12:102876040
|
AT | A | 72 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(69): Show | 73 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.441+1421delA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102876040 | ||||||
| chr12:102876258
|
A | G | 62 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(59): Show | 63 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.441+1204T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102876258 | ||||||
| chr12:102876395
|
G | A | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.441+1067C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102876395 | ||||||
| chr12:102876620
|
G | A | 11 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0013others(8): Show | 12 | HG00741.hp1 HG01081.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+842C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102876620 | ||||||
| chr12:102876676
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.441+786C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102876676 | ||||||
| chr12:102876679
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(74): Show | 79 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.441+783C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102876679 | ||||||
| chr12:102876743
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 74 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.441+719G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102876743 | ||||||
| chr12:102877016
|
G | A | 1 | a0001c0003t0003g0257 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.441+446C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102877016 | ||||||
| chr12:102877068
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 74 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.441+394C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102877068 | ||||||
| chr12:102877248
|
A | T | 5 | a0001c0001t0004g0295a0001c0001t0004g0296a0001c0006t0004g0292others(2): Show | 5 | HG02258.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+214T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102877248 | ||||||
| chr12:102877415
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(70): Show | 75 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.441+47C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102877415 | ||||||
| chr12:102877436
|
T | C | 15 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(12): Show | 15 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.441+26A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102877436 | ||||||
| chr12:102877442
|
C | T | 2 | a0001c0008t0001g0133a0001c0008t0001g0134 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.441+20G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 4/12 | chr12 | 102877442 | ||||||
| chr12:102877572
|
G | A | 76 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(73): Show | 78 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.353-22C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102877572 | ||||||
| chr12:102877639
|
A | G | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.353-89T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102877639 | ||||||
| chr12:102877688
|
C | T | 12 | a0001c0001t0012g0146a0001c0004t0001g0103a0001c0004t0001g0140others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.353-138G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102877688 | ||||||
| chr12:102877694
|
A | G | 1 | a0001c0003t0003g0265 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.353-144T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102877694 | ||||||
| chr12:102877722
|
C | T | 6 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.353-172G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102877722 | ||||||
| chr12:102877759
|
T | G | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.353-209A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102877759 | ||||||
| chr12:102877897
|
C | T | 1 | a0001c0001t0011g0132 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.353-347G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102877897 | ||||||
| chr12:102877969
|
G | A | 68 | a0001c0001t0002g0157a0001c0002t0001g0003a0001c0002t0001g0021others(65): Show | 70 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.353-419C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102877969 | ||||||
| chr12:102877982
|
T | C | 7 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(4): Show | 7 | HG01175.hp2 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.353-432A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102877982 | ||||||
| chr12:102877990
|
C | T | 70 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286others(67): Show | 72 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.353-440G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102877990 | ||||||
| chr12:102878296
|
T | A | 1 | a0001c0001t0002g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.353-746A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102878296 | ||||||
| chr12:102878302
|
C | T | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.353-752G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102878302 | ||||||
| chr12:102878404
|
T | G | 15 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0009others(12): Show | 16 | HG00741.hp1 HG01081.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.353-854A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102878404 | ||||||
| chr12:102878418
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.353-868G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102878418 | ||||||
| chr12:102878544
|
C | G | 70 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286others(67): Show | 72 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.353-994G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102878544 | ||||||
| chr12:102878604
|
G | A | 2 | a0001c0001t0001g0120a0001c0002t0001g0074 | 2 | NA19012.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.353-1054C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102878604 | ||||||
| chr12:102878682
|
CAAGAT | C | 5 | a0001c0001t0011g0132a0001c0004t0008g0300a0001c0004t0008g0301others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.353-1137_353-1133d others(7): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102878682 | ||||||
| chr12:102878866
|
C | T | 1 | a0001c0002t0001g0095 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.353-1316G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102878866 | ||||||
| chr12:102878908
|
G | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(250): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.353-1358C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102878908 | ||||||
| chr12:102879011
|
C | G | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.353-1461G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102879011 | ||||||
| chr12:102879032
|
G | T | 1 | a0001c0001t0002g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.353-1482C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102879032 | ||||||
| chr12:102879107
|
G | A | 1 | a0001c0003t0001g0204 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.353-1557C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102879107 | ||||||
| chr12:102879255
|
T | C | 1 | a0001c0002t0001g0055 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.353-1705A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102879255 | ||||||
| chr12:102879416
|
C | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(107): Show | 112 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.353-1866G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102879416 | ||||||
| chr12:102879532
|
A | G | 62 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(59): Show | 63 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.353-1982T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102879532 | ||||||
| chr12:102879604
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.353-2054C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102879604 | ||||||
| chr12:102879605
|
T | TG | 55 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(52): Show | 55 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.353-2056dupC | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102879605 | ||||||
| chr12:102879605
|
TG | T | 80 | a0001c0001t0001g0046a0001c0001t0001g0156a0001c0001t0001g0162others(77): Show | 82 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.353-2056delC | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102879605 | ||||||
| chr12:102879607
|
G | T | 3 | a0001c0001t0001g0018a0001c0001t0007g0016a0001c0001t0007g0017 | 3 | HG02922.hp1 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.353-2057C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102879607 | ||||||
| chr12:102879642
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.353-2092G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102879642 | ||||||
| chr12:102879758
|
G | A | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.353-2208C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102879758 | ||||||
| chr12:102879972
|
C | G | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.353-2422G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102879972 | ||||||
| chr12:102880040
|
T | C | 5 | a0001c0001t0011g0132a0001c0004t0008g0300a0001c0004t0008g0301others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.353-2490A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880040 | ||||||
| chr12:102880113
|
T | G | 6 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.353-2563A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880113 | ||||||
| chr12:102880149
|
T | C | 6 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.353-2599A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880149 | ||||||
| chr12:102880173
|
G | A | 6 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.353-2623C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880173 | ||||||
| chr12:102880182
|
C | T | 15 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0009others(12): Show | 16 | HG00741.hp1 HG01081.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.353-2632G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880182 | ||||||
| chr12:102880204
|
C | T | 2 | a0001c0003t0001g0204a0001c0006t0016g0163 | 2 | HG04228.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.353-2654G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880204 | ||||||
| chr12:102880220
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.353-2670A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880220 | ||||||
| chr12:102880241
|
T | C | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.353-2691A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880241 | ||||||
| chr12:102880305
|
G | C | 38 | a0001c0001t0001g0203a0001c0001t0002g0008a0001c0001t0002g0130others(35): Show | 38 | HG00642.hp2 HG01109.hp1 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.353-2755C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880305 | ||||||
| chr12:102880448
|
A | C | 3 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131 | 3 | HG01884.hp1 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.353-2898T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880448 | ||||||
| chr12:102880864
|
C | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(64): Show | 69 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.353-3314G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880864 | ||||||
| chr12:102880891
|
G | A | 6 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.353-3341C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880891 | ||||||
| chr12:102880948
|
T | G | 12 | a0001c0001t0012g0146a0001c0004t0001g0103a0001c0004t0001g0140others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.353-3398A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880948 | ||||||
| chr12:102880968
|
T | A | 254 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(251): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.353-3418A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102880968 | ||||||
| chr12:102881008
|
T | C | 58 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(55): Show | 59 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.353-3458A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881008 | ||||||
| chr12:102881100
|
G | A | 1 | a0001c0003t0003g0258 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.353-3550C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881100 | ||||||
| chr12:102881101
|
C | A | 2 | a0001c0001t0009g0298a0001c0001t0009g0299 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.353-3551G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881101 | ||||||
| chr12:102881107
|
G | A | 6 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.353-3557C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881107 | ||||||
| chr12:102881174
|
C | T | 63 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(60): Show | 64 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.353-3624G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881174 | ||||||
| chr12:102881233
|
C | G | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.353-3683G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881233 | ||||||
| chr12:102881360
|
T | C | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.353-3810A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881360 | ||||||
| chr12:102881361
|
A | G | 6 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.353-3811T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881361 | ||||||
| chr12:102881435
|
T | C | 6 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.353-3885A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881435 | ||||||
| chr12:102881457
|
C | T | 2 | a0001c0001t0001g0020a0001c0002t0011g0030 | 2 | HG00738.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.353-3907G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881457 | ||||||
| chr12:102881458
|
G | A | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.353-3908C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881458 | ||||||
| chr12:102881468
|
T | A | 1 | a0001c0001t0002g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.353-3918A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881468 | ||||||
| chr12:102881469
|
G | C | 2 | a0001c0001t0002g0216a0001c0012t0002g0214 | 2 | HG00323.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.353-3919C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881469 | ||||||
| chr12:102881680
|
T | C | 2 | a0001c0003t0005g0260a0001c0014t0003g0261 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.353-4130A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881680 | ||||||
| chr12:102881820
|
G | A | 2 | a0001c0001t0009g0298a0001c0001t0009g0299 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.353-4270C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102881820 | ||||||
| chr12:102882094
|
T | C | 187 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(184): Show | 190 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.353-4544A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882094 | ||||||
| chr12:102882104
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(79): Show | 84 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.353-4554C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882104 | ||||||
| chr12:102882123
|
C | T | 187 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(184): Show | 190 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.353-4573G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882123 | ||||||
| chr12:102882124
|
C | A | 1 | a0001c0003t0003g0288 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.353-4574G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882124 | ||||||
| chr12:102882138
|
A | G | 4 | a0001c0002t0001g0061a0001c0002t0001g0064a0001c0002t0001g0065others(1): Show | 4 | NA18985.hp2 NA18999.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.353-4588T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882138 | ||||||
| chr12:102882147
|
A | G | 5 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0296others(2): Show | 5 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.353-4597T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882147 | ||||||
| chr12:102882265
|
G | A | 2 | a0001c0003t0001g0204a0001c0006t0016g0163 | 2 | HG04228.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.353-4715C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882265 | ||||||
| chr12:102882437
|
G | A | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.353-4887C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882437 | ||||||
| chr12:102882576
|
GTA | G | 53 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(50): Show | 54 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.353-5028_353-5027d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882576 | ||||||
| chr12:102882642
|
C | CTA | 22 | a0001c0001t0001g0023a0001c0001t0001g0068a0001c0001t0001g0072others(19): Show | 23 | HG00099.hp2 HG00558.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.353-5094_353-5093d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882642 | ||||||
| chr12:102882642
|
C | CTATA | 21 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0052others(18): Show | 21 | HG00558.hp2 HG00735.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.353-5096_353-5093d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882642 | ||||||
| chr12:102882642
|
C | CTATATA | 10 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0159others(7): Show | 10 | HG00642.hp1 HG01106.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.353-5098_353-5093d others(8): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882642 | ||||||
| chr12:102882642
|
C | CTATATAT others(1): Show |
9 | a0001c0001t0001g0118a0001c0003t0003g0259a0002c0005t0003g0247others(6): Show | 9 | HG00735.hp2 NA18939.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.353-5100_353-5093d others(10): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882642 | ||||||
| chr12:102882642
|
C | CTATATAT others(3): Show |
1 | a0001c0003t0003g0280 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.353-5102_353-5093d others(12): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882642 | ||||||
| chr12:102882642
|
CTA | C | 5 | a0001c0003t0003g0267a0001c0003t0003g0268a0001c0003t0003g0272others(2): Show | 5 | HG00099.hp1 HG00609.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.353-5094_353-5093d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882642 | ||||||
| chr12:102882642
|
CTATA | C | 5 | a0001c0003t0003g0266a0001c0003t0003g0274a0001c0003t0003g0287others(2): Show | 5 | HG00408.hp2 HG00673.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.353-5096_353-5093d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882642 | ||||||
| chr12:102882642
|
CTATATAT others(7): Show |
C | 1 | a0001c0003t0003g0291 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.353-5106_353-5093d others(16): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882642 | ||||||
| chr12:102882659
|
TATATATA others(11): Show |
T | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.353-5127_353-5110d others(20): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882659 | ||||||
| chr12:102882661
|
TATATATA others(9): Show |
T | 78 | a0001c0001t0001g0096a0001c0001t0012g0146a0001c0002t0001g0003others(75): Show | 79 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.353-5127_353-5112d others(18): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882661 | ||||||
| chr12:102882663
|
TATATATA others(7): Show |
T | 55 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(52): Show | 56 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.353-5127_353-5114d others(16): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882663 | ||||||
| chr12:102882665
|
TATATATA others(5): Show |
T | 6 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0004g0232others(3): Show | 7 | HG00741.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.353-5127_353-5116d others(14): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882665 | ||||||
| chr12:102882667
|
TATATATA others(3): Show |
T | 12 | a0001c0001t0001g0156a0001c0001t0001g0221a0001c0001t0001g0222others(9): Show | 12 | HG01884.hp1 HG02572.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.353-5127_353-5118d others(12): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882667 | ||||||
| chr12:102882669
|
TATATATA others(1): Show |
T | 8 | a0001c0001t0002g0155a0001c0001t0002g0168a0001c0001t0002g0170others(5): Show | 8 | HG00639.hp2 HG01069.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.353-5127_353-5120d others(10): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882669 | ||||||
| chr12:102882671
|
TATATAA | T | 12 | a0001c0001t0001g0047a0001c0001t0002g0009a0001c0001t0002g0014others(9): Show | 12 | HG01167.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.353-5127_353-5122d others(8): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882671 | ||||||
| chr12:102882673
|
TATAA | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0041others(11): Show | 16 | HG00738.hp1 HG00741.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.353-5127_353-5124d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882673 | ||||||
| chr12:102882675
|
TAA | T | 18 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0071others(15): Show | 18 | HG01081.hp1 HG01099.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.353-5127_353-5126d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882675 | ||||||
| chr12:102882677
|
A | T | 49 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(46): Show | 49 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.353-5127T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882677 | ||||||
| chr12:102882775
|
T | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(78): Show | 83 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.353-5225A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882775 | ||||||
| chr12:102882834
|
A | T | 7 | a0001c0001t0003g0233a0001c0001t0009g0298a0001c0001t0009g0299others(4): Show | 7 | HG00642.hp2 HG01175.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.353-5284T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882834 | ||||||
| chr12:102882975
|
G | A | 2 | a0001c0008t0001g0133a0001c0008t0001g0134 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.353-5425C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102882975 | ||||||
| chr12:102883000
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.353-5450C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102883000 | ||||||
| chr12:102883113
|
G | A | 1 | a0001c0003t0003g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.353-5563C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102883113 | ||||||
| chr12:102883172
|
G | A | 45 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(42): Show | 45 | HG00642.hp2 HG01109.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.353-5622C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102883172 | ||||||
| chr12:102883387
|
C | T | 65 | a0001c0002t0001g0003a0001c0002t0001g0021a0001c0002t0001g0027others(62): Show | 67 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.353-5837G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102883387 | ||||||
| chr12:102883388
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.353-5838C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102883388 | ||||||
| chr12:102883444
|
C | T | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.353-5894G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102883444 | ||||||
| chr12:102883464
|
C | T | 47 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(44): Show | 47 | HG00642.hp2 HG01109.hp1 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.353-5914G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102883464 | ||||||
| chr12:102883650
|
G | A | 24 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(21): Show | 24 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.353-6100C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102883650 | ||||||
| chr12:102884060
|
G | A | 5 | a0001c0002t0001g0075a0001c0002t0001g0084a0001c0002t0001g0092others(2): Show | 5 | HG01496.hp2 HG01928.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.353-6510C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102884060 | ||||||
| chr12:102884061
|
C | T | 6 | a0001c0002t0001g0075a0001c0002t0001g0084a0001c0002t0001g0092others(3): Show | 6 | HG01496.hp2 HG01928.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.353-6511G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102884061 | ||||||
| chr12:102884233
|
C | A | 58 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(55): Show | 59 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.353-6683G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102884233 | ||||||
| chr12:102884247
|
C | T | 1 | a0001c0009t0005g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.353-6697G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102884247 | ||||||
| chr12:102884275
|
G | C | 58 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(55): Show | 59 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.353-6725C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102884275 | ||||||
| chr12:102884498
|
C | A | 1 | a0002c0005t0003g0247 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.353-6948G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102884498 | ||||||
| chr12:102884536
|
G | A | 61 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(58): Show | 62 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.353-6986C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102884536 | ||||||
| chr12:102884606
|
A | G | 38 | a0001c0001t0001g0162a0001c0001t0002g0008a0001c0001t0002g0130others(35): Show | 38 | HG00642.hp2 HG01109.hp1 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.353-7056T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102884606 | ||||||
| chr12:102884733
|
T | C | 3 | a0001c0001t0002g0210a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.353-7183A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102884733 | ||||||
| chr12:102884831
|
G | A | 1 | a0001c0002t0001g0095 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.353-7281C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102884831 | ||||||
| chr12:102884856
|
T | C | 6 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0296others(3): Show | 6 | HG02258.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.353-7306A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102884856 | ||||||
| chr12:102884967
|
C | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(84): Show | 89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.353-7417G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102884967 | ||||||
| chr12:102885033
|
T | G | 4 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0002t0001g0090others(1): Show | 4 | HG01257.hp1 HG01952.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.353-7483A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102885033 | ||||||
| chr12:102885372
|
A | C | 1 | a0001c0001t0001g0067 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.353-7822T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102885372 | ||||||
| chr12:102885456
|
G | A | 55 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(52): Show | 56 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.353-7906C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102885456 | ||||||
| chr12:102885475
|
G | A | 2 | a0001c0003t0001g0204a0001c0006t0016g0163 | 2 | HG04228.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.353-7925C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102885475 | ||||||
| chr12:102885479
|
G | A | 45 | a0001c0001t0002g0180a0001c0001t0003g0271a0001c0003t0001g0121others(42): Show | 46 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.353-7929C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102885479 | ||||||
| chr12:102885616
|
C | T | 1 | a0001c0004t0001g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.353-8066G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102885616 | ||||||
| chr12:102885864
|
A | C | 1 | a0001c0002t0001g0158 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.353-8314T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102885864 | ||||||
| chr12:102885930
|
A | T | 80 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(77): Show | 81 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(78): Show |
intron_variant | MODIFIER | c.353-8380T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102885930 | ||||||
| chr12:102885985
|
T | C | 11 | a0001c0001t0002g0216a0001c0001t0003g0233a0001c0001t0009g0298others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.353-8435A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102885985 | ||||||
| chr12:102886051
|
T | G | 2 | a0001c0002t0001g0097a0001c0002t0001g0154 | 2 | HG01993.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.353-8501A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102886051 | ||||||
| chr12:102886148
|
T | A | 6 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0296others(3): Show | 6 | HG02258.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.352+8587A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102886148 | ||||||
| chr12:102886204
|
G | A | 22 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(19): Show | 22 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.352+8531C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102886204 | ||||||
| chr12:102886212
|
T | G | 1 | a0001c0001t0002g0155 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.352+8523A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102886212 | ||||||
| chr12:102886338
|
G | T | 46 | a0001c0001t0003g0271a0001c0003t0001g0121a0001c0003t0003g0006others(43): Show | 47 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.352+8397C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102886338 | ||||||
| chr12:102886500
|
C | T | 1 | a0001c0007t0002g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.352+8235G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102886500 | ||||||
| chr12:102886757
|
T | C | 3 | a0001c0007t0010g0031a0001c0007t0010g0032a0001c0007t0010g0033 | 3 | HG02280.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.352+7978A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102886757 | ||||||
| chr12:102886948
|
C | T | 23 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(20): Show | 23 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.352+7787G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102886948 | ||||||
| chr12:102886978
|
G | C | 60 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(57): Show | 61 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.352+7757C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102886978 | ||||||
| chr12:102887055
|
A | G | 11 | a0001c0001t0002g0216a0001c0001t0003g0233a0001c0001t0009g0298others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.352+7680T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887055 | ||||||
| chr12:102887101
|
C | T | 11 | a0001c0001t0002g0216a0001c0001t0003g0233a0001c0001t0009g0298others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.352+7634G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887101 | ||||||
| chr12:102887107
|
G | A | 6 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0296others(3): Show | 6 | HG02258.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.352+7628C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887107 | ||||||
| chr12:102887392
|
C | T | 11 | a0001c0001t0002g0216a0001c0001t0003g0233a0001c0001t0009g0298others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.352+7343G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887392 | ||||||
| chr12:102887526
|
G | T | 2 | a0001c0001t0002g0173a0001c0001t0002g0174 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.352+7209C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887526 | ||||||
| chr12:102887528
|
C | A | 2 | a0001c0001t0002g0173a0001c0001t0002g0174 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.352+7207G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887528 | ||||||
| chr12:102887533
|
G | A | 2 | a0001c0002t0001g0051a0001c0002t0001g0059 | 2 | NA19065.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.352+7202C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887533 | ||||||
| chr12:102887589
|
G | A | 1 | a0001c0007t0002g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.352+7146C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887589 | ||||||
| chr12:102887644
|
A | G | 2 | a0001c0001t0004g0285a0001c0001t0004g0286 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.352+7091T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887644 | ||||||
| chr12:102887724
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.352+7011G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887724 | ||||||
| chr12:102887758
|
G | T | 11 | a0001c0001t0002g0216a0001c0001t0003g0233a0001c0001t0009g0298others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.352+6977C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887758 | ||||||
| chr12:102887836
|
T | C | 1 | a0001c0002t0001g0175 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.352+6899A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887836 | ||||||
| chr12:102887838
|
G | T | 6 | a0001c0001t0004g0285a0001c0001t0004g0286a0001c0004t0008g0300others(3): Show | 6 | HG02451.hp1 HG02486.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.352+6897C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887838 | ||||||
| chr12:102887861
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.352+6874G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887861 | ||||||
| chr12:102887900
|
A | T | 1 | a0001c0001t0002g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.352+6835T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887900 | ||||||
| chr12:102887935
|
G | A | 1 | a0001c0012t0002g0214 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.352+6800C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102887935 | ||||||
| chr12:102888363
|
A | C | 1 | a0001c0002t0003g0231 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.352+6372T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102888363 | ||||||
| chr12:102888369
|
A | T | 2 | a0001c0003t0001g0204a0001c0006t0016g0163 | 2 | HG04228.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.352+6366T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102888369 | ||||||
| chr12:102888427
|
C | T | 1 | a0001c0002t0001g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.352+6308G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102888427 | ||||||
| chr12:102888743
|
G | A | 6 | a0001c0001t0003g0233a0001c0001t0009g0298a0001c0001t0009g0299others(3): Show | 6 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.352+5992C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102888743 | ||||||
| chr12:102888748
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.352+5987C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102888748 | ||||||
| chr12:102888853
|
T | A | 1 | a0001c0001t0002g0155 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.352+5882A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102888853 | ||||||
| chr12:102889144
|
T | C | 13 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0009others(10): Show | 14 | HG00741.hp1 HG01167.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.352+5591A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889144 | ||||||
| chr12:102889153
|
T | A | 84 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(81): Show | 85 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.352+5582A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889153 | ||||||
| chr12:102889164
|
C | T | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+5571G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889164 | ||||||
| chr12:102889174
|
T | C | 95 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(92): Show | 96 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.352+5561A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889174 | ||||||
| chr12:102889205
|
G | T | 7 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(4): Show | 7 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+5530C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889205 | ||||||
| chr12:102889266
|
T | A | 2 | a0001c0001t0012g0146a0001c0004t0001g0143 | 2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.352+5469A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889266 | ||||||
| chr12:102889286
|
A | C | 4 | a0001c0009t0005g0235a0001c0009t0005g0236a0001c0009t0005g0238others(1): Show | 4 | HG02257.hp1 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+5449T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889286 | ||||||
| chr12:102889288
|
C | G | 2 | a0001c0008t0001g0133a0001c0008t0001g0134 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.352+5447G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889288 | ||||||
| chr12:102889402
|
C | CATAG | 21 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0067others(18): Show | 22 | HG00408.hp1 HG00558.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.352+5329_352+5332d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889402 | ||||||
| chr12:102889402
|
CATAG | C | 125 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0054others(122): Show | 125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.352+5329_352+5332d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889402 | ||||||
| chr12:102889402
|
CATAGATA others(1): Show |
C | 21 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0047others(18): Show | 22 | HG00639.hp2 HG00738.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.352+5325_352+5332d others(10): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889402 | ||||||
| chr12:102889402
|
CATAGATA others(5): Show |
C | 13 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0013others(10): Show | 14 | HG00741.hp1 HG01175.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.352+5321_352+5332d others(14): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889402 | ||||||
| chr12:102889470
|
CAGAT | C | 15 | a0001c0001t0002g0216a0001c0001t0003g0233a0001c0001t0009g0298others(12): Show | 15 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.352+5261_352+5264d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889470 | ||||||
| chr12:102889490
|
TGATA | T | 4 | a0001c0001t0002g0168a0001c0001t0002g0170a0001c0001t0002g0171others(1): Show | 4 | HG00639.hp2 HG01069.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+5241_352+5244d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889490 | ||||||
| chr12:102889533
|
C | A | 13 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0009others(10): Show | 14 | HG00741.hp1 HG01167.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.352+5202G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889533 | ||||||
| chr12:102889534
|
G | GGACA | 15 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0203others(12): Show | 15 | HG01109.hp1 HG01358.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.352+5200_352+5201i others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889534 | ||||||
| chr12:102889534
|
G | GGACAGAT others(1): Show |
61 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(58): Show | 62 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.352+5200_352+5201i others(10): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889534 | ||||||
| chr12:102889534
|
G | GGACAGAT others(5): Show |
15 | a0001c0001t0002g0131a0001c0001t0002g0165a0001c0001t0002g0168others(12): Show | 15 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.352+5200_352+5201i others(14): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889534 | ||||||
| chr12:102889534
|
G | GGACAGAT others(9): Show |
3 | a0001c0001t0001g0208a0001c0001t0002g0188a0001c0004t0001g0140 | 3 | HG02698.hp2 HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.352+5200_352+5201i others(18): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889534 | ||||||
| chr12:102889534
|
G | GGATA | 5 | a0001c0001t0002g0216a0001c0001t0003g0233a0001c0003t0001g0204others(2): Show | 5 | HG00323.hp2 HG00642.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+5197_352+5200d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889534 | ||||||
| chr12:102889534
|
G | GGATAGAT others(1): Show |
8 | a0001c0001t0009g0298a0001c0001t0009g0299a0001c0001t0009g0305others(5): Show | 8 | HG00639.hp1 HG00741.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.352+5193_352+5200d others(10): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889534 | ||||||
| chr12:102889534
|
G | GGATAGAT others(5): Show |
1 | a0001c0009t0005g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.352+5189_352+5200d others(14): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889534 | ||||||
| chr12:102889534
|
GGATAGAT others(5): Show |
G | 42 | a0001c0001t0003g0271a0001c0003t0001g0121a0001c0003t0003g0006others(39): Show | 43 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.352+5189_352+5200d others(14): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889534 | ||||||
| chr12:102889534
|
GGATAGAT others(13): Show |
G | 2 | a0001c0003t0003g0266a0001c0003t0003g0274 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.352+5181_352+5200d others(22): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889534 | ||||||
| chr12:102889537
|
T | C | 2 | a0001c0001t0004g0285a0001c0001t0004g0286 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.352+5198A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889537 | ||||||
| chr12:102889549
|
C | T | 111 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(108): Show | 112 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.352+5186G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889549 | ||||||
| chr12:102889553
|
T | G | 2 | a0001c0001t0002g0210a0001c0006t0002g0211 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.352+5182A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889553 | ||||||
| chr12:102889557
|
T | C | 2 | a0001c0003t0003g0266a0001c0003t0003g0274 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.352+5178A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889557 | ||||||
| chr12:102889721
|
A | G | 14 | a0001c0001t0002g0005a0001c0001t0002g0161a0001c0001t0002g0180others(11): Show | 15 | HG00323.hp1 HG01099.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.352+5014T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889721 | ||||||
| chr12:102889787
|
C | T | 7 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(4): Show | 7 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+4948G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889787 | ||||||
| chr12:102889801
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.352+4934G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889801 | ||||||
| chr12:102889808
|
C | T | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+4927G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102889808 | ||||||
| chr12:102890051
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.352+4684C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890051 | ||||||
| chr12:102890154
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.352+4581T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890154 | ||||||
| chr12:102890194
|
A | G | 289 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(286): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.352+4541T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890194 | ||||||
| chr12:102890214
|
A | C | 1 | a0001c0003t0003g0275 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.352+4521T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890214 | ||||||
| chr12:102890253
|
G | A | 4 | a0001c0009t0005g0235a0001c0009t0005g0236a0001c0009t0005g0238others(1): Show | 4 | HG02257.hp1 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+4482C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890253 | ||||||
| chr12:102890443
|
G | A | 25 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.352+4292C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890443 | ||||||
| chr12:102890492
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.352+4243C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890492 | ||||||
| chr12:102890533
|
G | A | 1 | a0001c0002t0001g0058 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.352+4202C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890533 | ||||||
| chr12:102890637
|
C | A | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.352+4098G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890637 | ||||||
| chr12:102890675
|
C | A | 1 | a0001c0001t0002g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.352+4060G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890675 | ||||||
| chr12:102890686
|
T | A | 1 | a0001c0001t0001g0207 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.352+4049A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890686 | ||||||
| chr12:102890733
|
T | C | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.352+4002A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890733 | ||||||
| chr12:102890777
|
C | G | 6 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0296others(3): Show | 6 | HG02258.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.352+3958G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890777 | ||||||
| chr12:102890929
|
A | G | 1 | a0001c0002t0001g0036 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.352+3806T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890929 | ||||||
| chr12:102890950
|
T | G | 177 | a0001c0001t0001g0018a0001c0001t0001g0156a0001c0001t0001g0162others(174): Show | 180 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.352+3785A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102890950 | ||||||
| chr12:102891265
|
A | T | 145 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(142): Show | 147 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.352+3470T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102891265 | ||||||
| chr12:102891297
|
C | A | 1 | a0001c0002t0001g0154 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.352+3438G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102891297 | ||||||
| chr12:102891328
|
T | A | 11 | a0001c0001t0002g0216a0001c0001t0003g0233a0001c0001t0009g0298others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.352+3407A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102891328 | ||||||
| chr12:102891494
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.352+3241G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102891494 | ||||||
| chr12:102891505
|
T | G | 11 | a0001c0001t0002g0216a0001c0001t0003g0233a0001c0001t0009g0298others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.352+3230A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102891505 | ||||||
| chr12:102891526
|
T | C | 1 | a0001c0012t0002g0214 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.352+3209A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102891526 | ||||||
| chr12:102891570
|
C | G | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+3165G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102891570 | ||||||
| chr12:102891577
|
G | A | 8 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.352+3158C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102891577 | ||||||
| chr12:102891730
|
C | T | 5 | a0001c0001t0002g0216a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.352+3005G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102891730 | ||||||
| chr12:102891875
|
C | A | 5 | a0001c0001t0006g0226a0001c0001t0006g0227a0001c0001t0006g0229others(2): Show | 5 | HG02630.hp1 HG02647.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.352+2860G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102891875 | ||||||
| chr12:102892034
|
A | G | 2 | a0001c0008t0001g0133a0001c0008t0001g0134 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.352+2701T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102892034 | ||||||
| chr12:102892384
|
G | GA | 181 | a0001c0001t0001g0018a0001c0001t0001g0156a0001c0001t0001g0162others(178): Show | 184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.352+2350dupT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102892384 | ||||||
| chr12:102892422
|
T | C | 153 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(150): Show | 155 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.352+2313A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102892422 | ||||||
| chr12:102892470
|
C | T | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.352+2265G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102892470 | ||||||
| chr12:102892577
|
A | G | 1 | a0001c0001t0002g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.352+2158T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102892577 | ||||||
| chr12:102892883
|
A | C | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+1852T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102892883 | ||||||
| chr12:102893027
|
C | T | 11 | a0001c0001t0002g0216a0001c0001t0003g0233a0001c0001t0009g0298others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.352+1708G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102893027 | ||||||
| chr12:102893028
|
T | A | 1 | a0001c0001t0004g0232 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.352+1707A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102893028 | ||||||
| chr12:102893177
|
T | A | 178 | a0001c0001t0001g0018a0001c0001t0001g0156a0001c0001t0001g0162others(175): Show | 181 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.352+1558A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102893177 | ||||||
| chr12:102893289
|
A | G | 61 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(58): Show | 62 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.352+1446T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102893289 | ||||||
| chr12:102893355
|
G | A | 2 | a0001c0001t0012g0146a0001c0004t0001g0143 | 2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.352+1380C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102893355 | ||||||
| chr12:102893401
|
A | AAAAAAT | 7 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0296others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.352+1328_352+1333d others(8): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102893401 | ||||||
| chr12:102893417
|
A | G | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+1318T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102893417 | ||||||
| chr12:102893420
|
A | AAAAATT | 46 | a0001c0001t0003g0271a0001c0003t0001g0121a0001c0003t0003g0006others(43): Show | 47 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.352+1314_352+1315i others(8): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102893420 | ||||||
| chr12:102893427
|
A | G | 1 | a0001c0002t0001g0074 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.352+1308T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102893427 | ||||||
| chr12:102893502
|
G | A | 8 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.352+1233C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102893502 | ||||||
| chr12:102893738
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.352+997A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102893738 | ||||||
| chr12:102893773
|
C | T | 2 | a0001c0008t0001g0133a0001c0008t0001g0134 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.352+962G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102893773 | ||||||
| chr12:102894169
|
C | T | 6 | a0001c0001t0003g0233a0001c0001t0009g0298a0001c0001t0009g0299others(3): Show | 6 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.352+566G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102894169 | ||||||
| chr12:102894192
|
T | G | 1 | a0001c0001t0001g0053 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.352+543A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102894192 | ||||||
| chr12:102894397
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.352+338A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102894397 | ||||||
| chr12:102894409
|
A | C | 1 | a0001c0001t0002g0212 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.352+326T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102894409 | ||||||
| chr12:102894429
|
T | TA | 178 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.352+305dupT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102894429 | ||||||
| chr12:102894478
|
T | C | 2 | a0001c0002t0001g0098a0001c0002t0001g0099 | 2 | HG00673.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.352+257A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102894478 | ||||||
| chr12:102894571
|
A | T | 62 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(59): Show | 62 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.352+164T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 3/12 | chr12 | 102894571 | ||||||
| chr12:102895076
|
G | C | 1 | a0001c0010t0001g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.169-158C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895076 | ||||||
| chr12:102895278
|
C | A | 61 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(58): Show | 62 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.169-360G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895278 | ||||||
| chr12:102895573
|
G | A | 25 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.169-655C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895573 | ||||||
| chr12:102895612
|
C | T | 6 | a0001c0001t0003g0233a0001c0001t0009g0298a0001c0001t0009g0299others(3): Show | 6 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-694G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895612 | ||||||
| chr12:102895635
|
T | C | 25 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.169-717A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895635 | ||||||
| chr12:102895735
|
A | G | 11 | a0001c0001t0002g0216a0001c0001t0003g0233a0001c0001t0009g0298others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-817T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895735 | ||||||
| chr12:102895820
|
A | G | 1 | a0001c0002t0001g0124 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.169-902T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895820 | ||||||
| chr12:102895833
|
C | T | 59 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(56): Show | 60 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.169-915G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895833 | ||||||
| chr12:102895854
|
CA | C | 13 | a0001c0001t0001g0054a0001c0001t0001g0091a0001c0001t0001g0135others(10): Show | 13 | HG01074.hp1 HG01255.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.169-937delT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895854 | ||||||
| chr12:102895854
|
CAA | C | 39 | a0001c0001t0001g0162a0001c0001t0002g0155a0001c0001t0003g0271others(36): Show | 39 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.169-938_169-937del others(2): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895854 | ||||||
| chr12:102895865
|
A | T | 4 | a0001c0001t0002g0170a0001c0001t0002g0172a0001c0001t0002g0193others(1): Show | 4 | HG00639.hp2 HG01069.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-947T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895865 | ||||||
| chr12:102895867
|
A | T | 48 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0187others(45): Show | 49 | HG00639.hp2 HG01069.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.169-949T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895867 | ||||||
| chr12:102895869
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0004g0286 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.169-952_169-951ins others(22): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895869 | ||||||
| chr12:102895869
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0004g0285 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.169-952_169-951ins others(21): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895869 | ||||||
| chr12:102895869
|
A | AAATAT | 8 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(5): Show | 8 | HG00639.hp1 HG01192.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-952_169-951ins others(5): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895869 | ||||||
| chr12:102895869
|
A | AAATATAT others(14): Show |
2 | a0001c0004t0008g0301a0001c0004t0008g0303 | 2 | HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.169-952_169-951ins others(21): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895869 | ||||||
| chr12:102895869
|
A | AAATATAT others(18): Show |
1 | a0001c0004t0008g0300 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.169-952_169-951ins others(25): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895869 | ||||||
| chr12:102895869
|
A | AAT | 12 | a0001c0001t0001g0068a0001c0001t0001g0128a0001c0001t0009g0298others(9): Show | 12 | HG00099.hp2 HG01099.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-953_169-952dup others(2): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895869 | ||||||
| chr12:102895869
|
A | AATATATA others(13): Show |
1 | a0001c0004t0008g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.169-971_169-952dup others(20): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895869 | ||||||
| chr12:102895869
|
A | AT | 4 | a0001c0001t0002g0004a0001c0001t0002g0151a0001c0001t0002g0152others(1): Show | 5 | HG00741.hp1 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-952_169-951ins others(1): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895869 | ||||||
| chr12:102895869
|
A | T | 83 | a0001c0001t0001g0104a0001c0001t0001g0156a0001c0001t0001g0179others(80): Show | 85 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.169-951T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895869 | ||||||
| chr12:102895869
|
AAT | A | 12 | a0001c0001t0001g0072a0001c0001t0002g0008a0001c0001t0002g0130others(9): Show | 12 | HG00735.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-953_169-952del others(2): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895869 | ||||||
| chr12:102895870
|
ATAT | A | 7 | a0001c0004t0007g0145a0001c0008t0001g0134a0001c0009t0005g0235others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-955_169-953del others(3): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895870 | ||||||
| chr12:102895871
|
T | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0118others(1): Show | 4 | HG02129.hp2 HG06807.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-953A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895871 | ||||||
| chr12:102895936
|
C | T | 2 | a0001c0008t0023g0242a0001c0008t0024g0241 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.169-1018G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895936 | ||||||
| chr12:102895975
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.169-1057C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102895975 | ||||||
| chr12:102896144
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.169-1226C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102896144 | ||||||
| chr12:102896219
|
C | T | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.169-1301G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102896219 | ||||||
| chr12:102896531
|
A | T | 92 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(89): Show | 93 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.169-1613T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102896531 | ||||||
| chr12:102896561
|
G | A | 47 | a0001c0001t0003g0271a0001c0003t0001g0121a0001c0003t0003g0006others(44): Show | 48 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.169-1643C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102896561 | ||||||
| chr12:102896904
|
T | C | 8 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-1986A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102896904 | ||||||
| chr12:102896923
|
C | T | 9 | a0001c0001t0001g0028a0001c0001t0001g0054a0001c0001t0001g0071others(6): Show | 9 | HG02280.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-2005G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102896923 | ||||||
| chr12:102896977
|
T | G | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.169-2059A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102896977 | ||||||
| chr12:102897129
|
C | T | 5 | a0001c0001t0002g0216a0001c0001t0009g0305a0001c0001t0009g0306others(2): Show | 5 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-2211G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897129 | ||||||
| chr12:102897291
|
A | AG | 47 | a0001c0001t0003g0271a0001c0003t0001g0121a0001c0003t0003g0006others(44): Show | 48 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.169-2374_169-2373i others(3): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897291 | ||||||
| chr12:102897292
|
A | AT | 16 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(13): Show | 16 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.169-2375dupA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897292 | ||||||
| chr12:102897292
|
A | T | 47 | a0001c0001t0003g0271a0001c0003t0001g0121a0001c0003t0003g0006others(44): Show | 48 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.169-2374T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897292 | ||||||
| chr12:102897451
|
ATG | A | 47 | a0001c0001t0001g0179a0001c0001t0001g0187a0001c0001t0001g0189others(44): Show | 48 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.169-2535_169-2534d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897451 | ||||||
| chr12:102897461
|
G | A | 5 | a0001c0009t0005g0235a0001c0009t0005g0236a0001c0009t0005g0238others(2): Show | 5 | HG02109.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-2543C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897461 | ||||||
| chr12:102897461
|
GTGTGTAT others(3): Show |
G | 47 | a0001c0001t0003g0271a0001c0003t0001g0121a0001c0003t0003g0006others(44): Show | 48 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.169-2553_169-2544d others(12): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897461 | ||||||
| chr12:102897463
|
G | A | 25 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.169-2545C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897463 | ||||||
| chr12:102897463
|
GTGTA | G | 4 | a0001c0001t0001g0203a0001c0001t0002g0168a0001c0001t0002g0171others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-2549_169-2546d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897463 | ||||||
| chr12:102897465
|
G | A | 42 | a0001c0001t0001g0162a0001c0001t0001g0184a0001c0001t0001g0186others(39): Show | 42 | HG01109.hp1 HG01243.hp1 HG01358.hp1 others(39): Show |
intron_variant | MODIFIER | c.169-2547C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897465 | ||||||
| chr12:102897465
|
G | GTA | 23 | a0001c0001t0001g0020a0001c0001t0001g0047a0001c0001t0001g0086others(20): Show | 23 | HG00609.hp2 HG00738.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.169-2549_169-2548d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897465 | ||||||
| chr12:102897465
|
G | GTATA | 4 | a0001c0002t0001g0064a0001c0002t0001g0065a0001c0002t0001g0066others(1): Show | 4 | NA18939.hp1 NA18985.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-2551_169-2548d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897465 | ||||||
| chr12:102897465
|
G | GTATATAT others(13): Show |
1 | a0001c0010t0001g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.169-2567_169-2548d others(22): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897465 | ||||||
| chr12:102897465
|
G | GTGTA | 6 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0038others(3): Show | 6 | HG04228.hp1 NA18944.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-2548_169-2547i others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897465 | ||||||
| chr12:102897465
|
GTA | G | 19 | a0001c0001t0001g0018a0001c0001t0001g0053a0001c0001t0001g0068others(16): Show | 20 | HG00099.hp2 HG00741.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.169-2549_169-2548d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897465 | ||||||
| chr12:102897465
|
GTATA | G | 4 | a0001c0001t0002g0216a0001c0001t0009g0305a0001c0001t0009g0306others(1): Show | 4 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-2551_169-2548d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897465 | ||||||
| chr12:102897465
|
GTATATA | G | 6 | a0001c0001t0003g0233a0001c0001t0009g0298a0001c0001t0009g0299others(3): Show | 6 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-2553_169-2548d others(8): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897465 | ||||||
| chr12:102897465
|
GTATATAT others(3): Show |
G | 7 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-2557_169-2548d others(12): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897465 | ||||||
| chr12:102897467
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.169-2549T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897467 | ||||||
| chr12:102897492
|
T | A | 54 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(51): Show | 55 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.169-2574A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897492 | ||||||
| chr12:102897492
|
T | TATACATA others(5): Show |
5 | a0001c0001t0002g0130a0001c0001t0011g0132a0001c0008t0001g0134others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-2575_169-2574i others(14): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897492 | ||||||
| chr12:102897492
|
T | TATATACA others(7): Show |
3 | a0001c0001t0002g0008a0001c0001t0002g0131a0001c0008t0001g0133 | 3 | HG01884.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.169-2575_169-2574i others(16): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897492 | ||||||
| chr12:102897492
|
T | TATATATA others(9): Show |
1 | a0001c0009t0005g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.169-2575_169-2574i others(18): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897492 | ||||||
| chr12:102897492
|
T | TATATATA others(3): Show |
1 | a0001c0004t0001g0149 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.169-2575_169-2574i others(12): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897492 | ||||||
| chr12:102897492
|
T | TATATATA others(11): Show |
2 | a0001c0009t0013g0240a0003c0013t0005g0237 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.169-2575_169-2574i others(20): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897492 | ||||||
| chr12:102897492
|
T | TATATATA others(5): Show |
2 | a0001c0004t0007g0145a0001c0015t0002g0148 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.169-2575_169-2574i others(14): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897492 | ||||||
| chr12:102897492
|
T | TATATATA others(13): Show |
1 | a0001c0009t0013g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.169-2575_169-2574i others(22): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897492 | ||||||
| chr12:102897492
|
T | TATATATA others(7): Show |
9 | a0001c0001t0004g0285a0001c0001t0004g0294a0001c0004t0001g0141others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-2575_169-2574i others(16): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897492 | ||||||
| chr12:102897492
|
T | TATATATA others(15): Show |
1 | a0001c0001t0002g0155 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.169-2575_169-2574i others(24): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897492 | ||||||
| chr12:102897492
|
T | TATATATA others(9): Show |
6 | a0001c0001t0004g0286a0001c0001t0004g0295a0001c0001t0004g0296others(3): Show | 6 | HG02258.hp1 HG02897.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-2575_169-2574i others(18): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897492 | ||||||
| chr12:102897492
|
T | TATATATA others(11): Show |
4 | a0001c0001t0012g0146a0001c0004t0001g0103a0001c0004t0001g0144others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-2575_169-2574i others(20): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897492 | ||||||
| chr12:102897492
|
T | TATATATA others(13): Show |
2 | a0001c0001t0004g0232a0001c0006t0004g0297 | 2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.169-2575_169-2574i others(22): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897492 | ||||||
| chr12:102897578
|
C | T | 4 | a0001c0001t0002g0216a0001c0001t0009g0305a0001c0001t0009g0306others(1): Show | 4 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-2660G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897578 | ||||||
| chr12:102897632
|
A | C | 67 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(64): Show | 68 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.169-2714T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897632 | ||||||
| chr12:102897696
|
G | C | 1 | a0001c0001t0002g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.169-2778C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897696 | ||||||
| chr12:102897711
|
C | T | 13 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0009others(10): Show | 14 | HG00741.hp1 HG01167.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-2793G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897711 | ||||||
| chr12:102897831
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.169-2913T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102897831 | ||||||
| chr12:102898029
|
T | C | 61 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(58): Show | 62 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.169-3111A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102898029 | ||||||
| chr12:102898105
|
C | T | 47 | a0001c0001t0003g0271a0001c0003t0001g0121a0001c0003t0003g0006others(44): Show | 48 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.169-3187G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102898105 | ||||||
| chr12:102898245
|
G | GT | 165 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(162): Show | 167 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.169-3328_169-3327i others(3): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102898245 | ||||||
| chr12:102898514
|
T | A | 13 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0009others(10): Show | 14 | HG00741.hp1 HG01167.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-3596A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102898514 | ||||||
| chr12:102898521
|
A | G | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-3603T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102898521 | ||||||
| chr12:102898593
|
C | T | 106 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(103): Show | 108 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.169-3675G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102898593 | ||||||
| chr12:102898617
|
T | G | 1 | a0001c0002t0001g0090 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.169-3699A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102898617 | ||||||
| chr12:102898760
|
T | C | 2 | a0001c0008t0023g0242a0001c0008t0024g0241 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.169-3842A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102898760 | ||||||
| chr12:102898994
|
A | C | 104 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0218others(101): Show | 104 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.169-4076T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102898994 | ||||||
| chr12:102899052
|
C | T | 1 | a0001c0001t0002g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.169-4134G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899052 | ||||||
| chr12:102899351
|
C | A | 1 | a0001c0001t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-4433G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899351 | ||||||
| chr12:102899445
|
C | T | 59 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(56): Show | 60 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.169-4527G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899445 | ||||||
| chr12:102899519
|
A | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0067a0001c0001t0001g0159 | 3 | HG00642.hp1 HG01106.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.169-4601T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899519 | ||||||
| chr12:102899582
|
G | A | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-4664C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899582 | ||||||
| chr12:102899679
|
G | A | 1 | a0001c0006t0004g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.169-4761C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899679 | ||||||
| chr12:102899729
|
G | A | 2 | a0001c0001t0004g0285a0001c0001t0004g0286 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.169-4811C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899729 | ||||||
| chr12:102899775
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.169-4857G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899775 | ||||||
| chr12:102899858
|
C | CA | 66 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(63): Show | 67 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.169-4941dupT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAA | 47 | a0001c0001t0001g0091a0001c0001t0003g0271a0001c0001t0012g0190others(44): Show | 49 | HG00099.hp1 HG00609.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.169-4942_169-4941d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAA | 30 | a0001c0001t0001g0096a0001c0001t0002g0177a0001c0002t0001g0039others(27): Show | 30 | HG00408.hp2 HG00597.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.169-4943_169-4941d others(5): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(1): Show |
10 | a0001c0001t0002g0174a0001c0001t0002g0180a0001c0001t0002g0183others(7): Show | 10 | HG01099.hp1 HG01346.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-4948_169-4941d others(10): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(2): Show |
13 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0161others(10): Show | 14 | HG01261.hp2 HG02004.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-4949_169-4941d others(11): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0002g0151a0001c0001t0004g0262a0001c0004t0001g0147others(2): Show | 5 | HG00323.hp1 HG01243.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-4950_169-4941d others(12): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(4): Show |
7 | a0001c0001t0001g0199a0001c0001t0002g0004a0001c0001t0002g0009others(4): Show | 8 | HG00741.hp1 HG01167.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-4951_169-4941d others(13): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0002g0169a0001c0001t0007g0015 | 2 | HG01433.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.169-4952_169-4941d others(14): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0018a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG02622.hp1 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-4953_169-4941d others(15): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0002g0155a0001c0001t0006g0226a0001c0001t0007g0017others(1): Show | 4 | HG02630.hp1 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-4954_169-4941d others(16): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0002g0010a0001c0001t0002g0166a0001c0001t0006g0227 | 3 | HG01993.hp2 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.169-4955_169-4941d others(17): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0002g0167a0001c0001t0002g0210 | 2 | HG01952.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.169-4956_169-4941d others(18): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(10): Show |
5 | a0001c0001t0001g0156a0001c0001t0002g0011a0001c0001t0004g0232others(2): Show | 5 | HG02559.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-4957_169-4941d others(19): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0162a0001c0001t0006g0230 | 2 | HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.169-4958_169-4941d others(20): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0002g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.169-4960_169-4941d others(22): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0002g0170 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.169-4963_169-4941d others(25): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(17): Show |
6 | a0001c0001t0001g0186a0001c0001t0001g0202a0001c0001t0002g0164others(3): Show | 6 | HG00639.hp2 HG01358.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-4964_169-4941d others(26): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(18): Show |
3 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0003t0001g0204 | 3 | HG04204.hp1 NA18963.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.169-4965_169-4941d others(27): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(22): Show |
2 | a0001c0001t0001g0184a0001c0002t0001g0209 | 2 | NA18942.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.169-4969_169-4941d others(31): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(23): Show |
2 | a0001c0001t0002g0205a0001c0001t0002g0225 | 2 | HG01106.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.169-4941_169-4940i others(32): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(24): Show |
2 | a0001c0001t0001g0179a0001c0001t0001g0187 | 2 | NA18992.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.169-4941_169-4940i others(33): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(25): Show |
2 | a0001c0001t0001g0206a0001c0002t0001g0185 | 2 | NA18957.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.169-4941_169-4940i others(34): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(26): Show |
1 | a0001c0002t0001g0175 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.169-4941_169-4940i others(35): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
C | CAAAAAAA others(29): Show |
1 | a0001c0001t0001g0207 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.169-4941_169-4940i others(38): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
CA | C | 6 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0009g0298others(3): Show | 6 | HG01175.hp2 HG01891.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-4941delT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899858
|
CAA | C | 6 | a0001c0001t0001g0218a0001c0001t0001g0223a0001c0001t0002g0216others(3): Show | 6 | HG00642.hp2 HG00741.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-4942_169-4941d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899858 | ||||||
| chr12:102899886
|
A | AAAAAAAA others(24): Show |
1 | a0001c0001t0002g0224 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.169-4969_169-4968i others(33): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899886 | ||||||
| chr12:102899921
|
A | G | 49 | a0001c0001t0003g0271a0001c0001t0004g0285a0001c0001t0004g0286others(46): Show | 50 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.169-5003T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899921 | ||||||
| chr12:102899959
|
G | A | 47 | a0001c0001t0003g0271a0001c0003t0001g0121a0001c0003t0003g0006others(44): Show | 48 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.169-5041C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102899959 | ||||||
| chr12:102900009
|
T | C | 86 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(83): Show | 87 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(84): Show |
intron_variant | MODIFIER | c.169-5091A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102900009 | ||||||
| chr12:102900049
|
C | CT | 21 | a0001c0001t0001g0041a0001c0001t0001g0186a0001c0001t0001g0187others(18): Show | 22 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.169-5132dupA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102900049 | ||||||
| chr12:102900049
|
CT | C | 73 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0009others(70): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.169-5132delA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102900049 | ||||||
| chr12:102900139
|
T | C | 47 | a0001c0001t0003g0271a0001c0003t0001g0121a0001c0003t0003g0006others(44): Show | 48 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.169-5221A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102900139 | ||||||
| chr12:102900200
|
T | C | 128 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(125): Show | 130 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.169-5282A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102900200 | ||||||
| chr12:102900317
|
G | A | 12 | a0001c0001t0012g0146a0001c0004t0001g0103a0001c0004t0001g0140others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-5399C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102900317 | ||||||
| chr12:102900318
|
G | T | 25 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.169-5400C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102900318 | ||||||
| chr12:102900329
|
G | C | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.169-5411C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102900329 | ||||||
| chr12:102900421
|
T | G | 63 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.169-5503A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102900421 | ||||||
| chr12:102900477
|
G | A | 67 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(64): Show | 68 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.169-5559C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102900477 | ||||||
| chr12:102900482
|
G | A | 67 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(64): Show | 68 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.169-5564C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102900482 | ||||||
| chr12:102900520
|
T | G | 61 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(58): Show | 62 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.169-5602A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102900520 | ||||||
| chr12:102901018
|
C | G | 1 | a0001c0001t0002g0212 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.169-6100G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901018 | ||||||
| chr12:102901100
|
A | G | 3 | a0001c0007t0010g0031a0001c0007t0010g0032a0001c0007t0010g0033 | 3 | HG02280.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.169-6182T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901100 | ||||||
| chr12:102901200
|
G | A | 287 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(284): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.169-6282C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901200 | ||||||
| chr12:102901233
|
C | T | 177 | a0001c0001t0001g0018a0001c0001t0001g0156a0001c0001t0001g0162others(174): Show | 180 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.169-6315G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901233 | ||||||
| chr12:102901255
|
T | C | 1 | a0001c0002t0001g0101 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.169-6337A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901255 | ||||||
| chr12:102901276
|
G | A | 67 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(64): Show | 68 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.169-6358C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901276 | ||||||
| chr12:102901620
|
C | T | 25 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.169-6702G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901620 | ||||||
| chr12:102901673
|
G | A | 1 | a0001c0004t0001g0149 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.169-6755C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901673 | ||||||
| chr12:102901674
|
G | A | 61 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(58): Show | 62 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.169-6756C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901674 | ||||||
| chr12:102901704
|
A | G | 86 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(83): Show | 87 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(84): Show |
intron_variant | MODIFIER | c.169-6786T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901704 | ||||||
| chr12:102901738
|
G | C | 1 | a0001c0002t0001g0102 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.169-6820C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901738 | ||||||
| chr12:102901858
|
G | A | 63 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 64 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.169-6940C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901858 | ||||||
| chr12:102901903
|
C | G | 41 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0001g0186others(38): Show | 42 | HG00323.hp1 HG01099.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.169-6985G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901903 | ||||||
| chr12:102901905
|
G | GA | 7 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-6988dupT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102901905 | ||||||
| chr12:102902101
|
A | C | 1 | a0001c0001t0002g0151 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.169-7183T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102902101 | ||||||
| chr12:102902189
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.169-7271A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102902189 | ||||||
| chr12:102902227
|
A | G | 306 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(303): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.169-7309T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102902227 | ||||||
| chr12:102902230
|
G | T | 148 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(145): Show | 150 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.169-7312C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102902230 | ||||||
| chr12:102902259
|
C | T | 1 | a0001c0007t0002g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.169-7341G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102902259 | ||||||
| chr12:102902264
|
G | C | 1 | a0001c0006t0001g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.169-7346C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102902264 | ||||||
| chr12:102902429
|
C | A | 2 | a0001c0008t0001g0133a0001c0008t0001g0134 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.169-7511G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102902429 | ||||||
| chr12:102902535
|
G | T | 49 | a0001c0001t0003g0271a0001c0001t0004g0285a0001c0001t0004g0286others(46): Show | 50 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.169-7617C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102902535 | ||||||
| chr12:102902608
|
T | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0002g0105others(2): Show | 5 | HG02615.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-7690A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102902608 | ||||||
| chr12:102902668
|
A | G | 6 | a0001c0002t0001g0034a0001c0002t0001g0036a0001c0002t0001g0037others(3): Show | 6 | HG00597.hp1 NA18944.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-7750T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102902668 | ||||||
| chr12:102902688
|
A | G | 8 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-7770T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102902688 | ||||||
| chr12:102902860
|
T | G | 49 | a0001c0001t0003g0271a0001c0001t0004g0285a0001c0001t0004g0286others(46): Show | 50 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.169-7942A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102902860 | ||||||
| chr12:102902927
|
T | A | 37 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(34): Show | 37 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.169-8009A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102902927 | ||||||
| chr12:102903066
|
A | G | 1 | a0001c0001t0002g0216 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.169-8148T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903066 | ||||||
| chr12:102903158
|
C | T | 13 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0009others(10): Show | 14 | HG00741.hp1 HG01167.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-8240G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903158 | ||||||
| chr12:102903189
|
C | T | 4 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167others(1): Show | 4 | HG01928.hp1 HG01952.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-8271G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903189 | ||||||
| chr12:102903315
|
C | T | 1 | a0001c0008t0018g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.169-8397G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903315 | ||||||
| chr12:102903352
|
T | G | 1 | a0001c0001t0001g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.169-8434A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903352 | ||||||
| chr12:102903360
|
C | CA | 83 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(80): Show | 84 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.169-8443dupT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903360 | ||||||
| chr12:102903360
|
C | CAA | 31 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0009others(28): Show | 32 | HG00323.hp2 HG00642.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.169-8444_169-8443d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903360 | ||||||
| chr12:102903360
|
C | CAAA | 6 | a0001c0009t0005g0235a0001c0009t0005g0236a0001c0009t0005g0238others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-8445_169-8443d others(5): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903360 | ||||||
| chr12:102903371
|
A | AC | 42 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(39): Show | 43 | HG00323.hp1 HG01099.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.169-8454_169-8453i others(3): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903371 | ||||||
| chr12:102903373
|
C | A | 1 | a0001c0003t0001g0107 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.169-8455G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903373 | ||||||
| chr12:102903385
|
C | A | 1 | a0001c0002t0001g0108 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.169-8467G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903385 | ||||||
| chr12:102903385
|
C | CACAA | 8 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG00639.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-8468_169-8467i others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903385 | ||||||
| chr12:102903387
|
A | C | 43 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(40): Show | 44 | HG00323.hp1 HG01099.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.169-8469T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903387 | ||||||
| chr12:102903388
|
A | AAC | 122 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0008others(119): Show | 124 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.169-8471_169-8470i others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903388 | ||||||
| chr12:102903388
|
A | C | 8 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG00639.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-8470T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903388 | ||||||
| chr12:102903400
|
A | C | 12 | a0001c0001t0001g0162a0001c0001t0002g0216a0001c0001t0003g0233others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-8482T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903400 | ||||||
| chr12:102903411
|
TTATG | T | 173 | a0001c0001t0001g0018a0001c0001t0001g0156a0001c0001t0001g0162others(170): Show | 176 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.169-8497_169-8494d others(6): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903411 | ||||||
| chr12:102903420
|
G | A | 6 | a0001c0009t0005g0235a0001c0009t0005g0236a0001c0009t0005g0238others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-8502C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903420 | ||||||
| chr12:102903563
|
G | C | 49 | a0001c0001t0003g0271a0001c0001t0004g0285a0001c0001t0004g0286others(46): Show | 50 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.169-8645C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903563 | ||||||
| chr12:102903788
|
C | T | 8 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-8870G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903788 | ||||||
| chr12:102903797
|
T | C | 1 | a0001c0002t0001g0109 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.169-8879A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903797 | ||||||
| chr12:102903805
|
G | A | 2 | a0001c0001t0004g0285a0001c0001t0004g0286 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.169-8887C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903805 | ||||||
| chr12:102903902
|
C | T | 19 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(16): Show | 19 | HG00639.hp2 HG01069.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.168+8889G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903902 | ||||||
| chr12:102903968
|
A | G | 180 | a0001c0001t0001g0018a0001c0001t0001g0156a0001c0001t0001g0162others(177): Show | 183 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.168+8823T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102903968 | ||||||
| chr12:102904045
|
T | C | 2 | a0001c0008t0001g0133a0001c0008t0001g0134 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.168+8746A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102904045 | ||||||
| chr12:102904140
|
C | G | 1 | a0001c0002t0011g0030 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.168+8651G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102904140 | ||||||
| chr12:102904269
|
A | G | 1 | a0001c0002t0001g0029 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.168+8522T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102904269 | ||||||
| chr12:102904279
|
C | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+8512G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102904279 | ||||||
| chr12:102904297
|
C | A | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.168+8494G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102904297 | ||||||
| chr12:102904504
|
T | C | 1 | a0001c0002t0001g0117 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.168+8287A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102904504 | ||||||
| chr12:102904593
|
T | A | 19 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(16): Show | 19 | HG00639.hp2 HG01069.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.168+8198A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102904593 | ||||||
| chr12:102904636
|
A | G | 2 | a0001c0003t0003g0287a0001c0003t0003g0288 | 2 | HG00408.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.168+8155T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102904636 | ||||||
| chr12:102904739
|
A | G | 170 | a0001c0001t0001g0018a0001c0001t0001g0156a0001c0001t0001g0162others(167): Show | 173 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.168+8052T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102904739 | ||||||
| chr12:102904809
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG00140.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.168+7982C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102904809 | ||||||
| chr12:102904834
|
C | G | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.168+7957G>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102904834 | ||||||
| chr12:102904837
|
T | C | 1 | a0001c0007t0002g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.168+7954A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102904837 | ||||||
| chr12:102905026
|
C | T | 43 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(40): Show | 44 | HG00323.hp1 HG01099.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.168+7765G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102905026 | ||||||
| chr12:102905065
|
G | A | 43 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(40): Show | 44 | HG00323.hp1 HG01099.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.168+7726C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102905065 | ||||||
| chr12:102905147
|
C | T | 43 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(40): Show | 44 | HG00323.hp1 HG01099.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.168+7644G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102905147 | ||||||
| chr12:102905161
|
T | C | 11 | a0001c0001t0002g0216a0001c0001t0003g0233a0001c0001t0009g0298others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+7630A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102905161 | ||||||
| chr12:102905553
|
G | GT | 4 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(1): Show | 4 | HG01167.hp2 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+7237dupA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102905553 | ||||||
| chr12:102905557
|
T | C | 18 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(15): Show | 18 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+7234A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102905557 | ||||||
| chr12:102905825
|
TA | T | 25 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0184others(22): Show | 25 | HG01099.hp1 HG01109.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.168+6965delT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102905825 | ||||||
| chr12:102905851
|
T | C | 173 | a0001c0001t0001g0018a0001c0001t0001g0156a0001c0001t0001g0162others(170): Show | 176 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.168+6940A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102905851 | ||||||
| chr12:102906004
|
T | C | 57 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(54): Show | 58 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.168+6787A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102906004 | ||||||
| chr12:102906023
|
G | A | 11 | a0001c0001t0012g0146a0001c0004t0001g0140a0001c0004t0001g0141others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+6768C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102906023 | ||||||
| chr12:102906160
|
A | C | 8 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+6631T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102906160 | ||||||
| chr12:102906544
|
T | C | 8 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+6247A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102906544 | ||||||
| chr12:102906629
|
C | T | 12 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0296others(9): Show | 12 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+6162G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102906629 | ||||||
| chr12:102906706
|
G | A | 1 | a0001c0002t0001g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.168+6085C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102906706 | ||||||
| chr12:102907170
|
G | T | 2 | a0001c0006t0004g0292a0001c0006t0004g0293 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.168+5621C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102907170 | ||||||
| chr12:102907184
|
T | C | 57 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(54): Show | 58 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.168+5607A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102907184 | ||||||
| chr12:102907364
|
C | T | 1 | a0001c0002t0001g0119 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.168+5427G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102907364 | ||||||
| chr12:102907398
|
A | C | 49 | a0001c0001t0003g0271a0001c0001t0004g0285a0001c0001t0004g0286others(46): Show | 50 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.168+5393T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102907398 | ||||||
| chr12:102907582
|
G | T | 49 | a0001c0001t0003g0271a0001c0001t0004g0285a0001c0001t0004g0286others(46): Show | 50 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.168+5209C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102907582 | ||||||
| chr12:102907733
|
C | T | 49 | a0001c0001t0003g0271a0001c0001t0004g0285a0001c0001t0004g0286others(46): Show | 50 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.168+5058G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102907733 | ||||||
| chr12:102908022
|
GA | G | 19 | a0001c0001t0012g0146a0001c0004t0001g0140a0001c0004t0001g0141others(16): Show | 19 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.168+4768delT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908022 | ||||||
| chr12:102908050
|
A | T | 1 | a0001c0002t0001g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.168+4741T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908050 | ||||||
| chr12:102908133
|
A | G | 1 | a0001c0009t0013g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.168+4658T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908133 | ||||||
| chr12:102908190
|
C | T | 19 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(16): Show | 19 | HG00639.hp2 HG01069.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.168+4601G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908190 | ||||||
| chr12:102908205
|
C | T | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.168+4586G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908205 | ||||||
| chr12:102908220
|
C | T | 9 | a0001c0001t0003g0233a0001c0001t0009g0298a0001c0001t0009g0299others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+4571G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908220 | ||||||
| chr12:102908221
|
G | GAC | 25 | a0001c0001t0001g0018a0001c0001t0002g0009a0001c0001t0002g0010others(22): Show | 25 | HG00741.hp1 HG01167.hp2 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.168+4568_168+4569d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908221 | ||||||
| chr12:102908221
|
G | GACACAC | 5 | a0001c0009t0005g0235a0001c0009t0005g0238a0001c0009t0013g0239others(2): Show | 5 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+4564_168+4569d others(8): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908221 | ||||||
| chr12:102908221
|
GAC | G | 82 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(79): Show | 83 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.168+4568_168+4569d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908221 | ||||||
| chr12:102908353
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.168+4438T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908353 | ||||||
| chr12:102908516
|
C | T | 47 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(44): Show | 48 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.168+4275G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908516 | ||||||
| chr12:102908655
|
TTATGAAC others(1): Show |
T | 175 | a0001c0001t0001g0018a0001c0001t0001g0156a0001c0001t0001g0162others(172): Show | 178 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.168+4128_168+4135d others(10): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908655 | ||||||
| chr12:102908837
|
C | CT | 45 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(42): Show | 46 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.168+3953dupA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908837 | ||||||
| chr12:102908837
|
C | CTT | 18 | a0001c0001t0001g0179a0001c0001t0002g0164a0001c0001t0002g0165others(15): Show | 18 | HG01069.hp2 HG01169.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+3952_168+3953d others(4): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908837 | ||||||
| chr12:102908837
|
CT | C | 16 | a0001c0001t0001g0156a0001c0001t0001g0219a0001c0001t0001g0220others(13): Show | 16 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+3953delA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908837 | ||||||
| chr12:102908866
|
A | G | 50 | a0001c0001t0003g0271a0001c0001t0004g0262a0001c0001t0004g0285others(47): Show | 51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.168+3925T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102908866 | ||||||
| chr12:102909018
|
G | A | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | NA18954.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.168+3773C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909018 | ||||||
| chr12:102909081
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.168+3710C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909081 | ||||||
| chr12:102909084
|
T | C | 50 | a0001c0001t0003g0271a0001c0001t0004g0262a0001c0001t0004g0285others(47): Show | 51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.168+3707A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909084 | ||||||
| chr12:102909118
|
G | A | 46 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(43): Show | 47 | HG00323.hp2 HG00558.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.168+3673C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909118 | ||||||
| chr12:102909171
|
G | A | 46 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(43): Show | 47 | HG00323.hp2 HG00558.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.168+3620C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909171 | ||||||
| chr12:102909396
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.168+3395T>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909396 | ||||||
| chr12:102909526
|
C | T | 6 | a0001c0001t0003g0233a0001c0001t0009g0298a0001c0001t0009g0299others(3): Show | 6 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+3265G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909526 | ||||||
| chr12:102909629
|
T | C | 100 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(97): Show | 102 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.168+3162A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909629 | ||||||
| chr12:102909681
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG00558.hp1 NA18966.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+3110G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909681 | ||||||
| chr12:102909711
|
C | T | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0007t0002g0178 | 3 | HG02451.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.168+3080G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909711 | ||||||
| chr12:102909713
|
C | A | 6 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0296others(3): Show | 6 | HG02258.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+3078G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909713 | ||||||
| chr12:102909716
|
T | C | 22 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0009others(19): Show | 23 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.168+3075A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909716 | ||||||
| chr12:102909770
|
G | A | 2 | a0001c0001t0002g0210a0001c0006t0002g0211 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.168+3021C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909770 | ||||||
| chr12:102909873
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.168+2918G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909873 | ||||||
| chr12:102909891
|
G | A | 1 | a0001c0003t0003g0291 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.168+2900C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909891 | ||||||
| chr12:102909923
|
C | T | 20 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(17): Show | 20 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.168+2868G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102909923 | ||||||
| chr12:102910365
|
G | A | 53 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(50): Show | 54 | HG00323.hp2 HG00558.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.168+2426C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102910365 | ||||||
| chr12:102910372
|
C | CT | 12 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(9): Show | 12 | HG00735.hp1 HG00735.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+2418dupA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102910372 | ||||||
| chr12:102910386
|
T | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0223a0001c0001t0002g0212others(4): Show | 7 | HG00323.hp2 HG01192.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+2405A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102910386 | ||||||
| chr12:102910387
|
T | G | 68 | a0001c0001t0001g0018a0001c0001t0001g0118a0001c0001t0001g0120others(65): Show | 70 | HG00323.hp2 HG00558.hp2 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.168+2404A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102910387 | ||||||
| chr12:102910387
|
TG | T | 18 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167others(15): Show | 18 | HG00639.hp2 HG01069.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+2403delC | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102910387 | ||||||
| chr12:102910388
|
G | T | 91 | a0001c0001t0002g0008a0001c0001t0002g0130a0001c0001t0002g0131others(88): Show | 92 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.168+2403C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102910388 | ||||||
| chr12:102910393
|
G | T | 157 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(154): Show | 159 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.168+2398C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102910393 | ||||||
| chr12:102910499
|
T | C | 1 | a0001c0001t0002g0217 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.168+2292A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102910499 | ||||||
| chr12:102910643
|
T | TCAACTC | 6 | a0001c0009t0005g0235a0001c0009t0005g0236a0001c0009t0005g0238others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+2147_168+2148i others(8): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102910643 | ||||||
| chr12:102910811
|
T | TCAACGTG others(8): Show |
13 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0009others(10): Show | 14 | HG00741.hp1 HG01167.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+1979_168+1980i others(17): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102910811 | ||||||
| chr12:102911137
|
C | A | 6 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(3): Show | 6 | HG00408.hp1 HG02129.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+1654G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102911137 | ||||||
| chr12:102911267
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 4 | HG01074.hp2 HG01099.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+1524A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102911267 | ||||||
| chr12:102911312
|
G | A | 6 | a0001c0009t0005g0235a0001c0009t0005g0236a0001c0009t0005g0238others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+1479C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102911312 | ||||||
| chr12:102911443
|
C | A | 138 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(135): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.168+1348G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102911443 | ||||||
| chr12:102911631
|
G | A | 156 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(153): Show | 158 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.168+1160C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102911631 | ||||||
| chr12:102911718
|
A | C | 1 | a0001c0002t0001g0021 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.168+1073T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102911718 | ||||||
| chr12:102912061
|
T | G | 7 | a0001c0001t0001g0156a0001c0001t0001g0218a0001c0001t0001g0219others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+730A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102912061 | ||||||
| chr12:102912269
|
C | T | 1 | a0001c0006t0016g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.168+522G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102912269 | ||||||
| chr12:102912281
|
T | C | 54 | a0001c0001t0003g0255a0001c0001t0003g0271a0001c0001t0004g0262others(51): Show | 55 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.168+510A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102912281 | ||||||
| chr12:102912524
|
T | A | 3 | a0001c0001t0009g0305a0001c0001t0009g0306a0001c0004t0026g0304 | 3 | HG00639.hp1 HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.168+267A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102912524 | ||||||
| chr12:102912772
|
A | G | 72 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(69): Show | 73 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.168+19T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 2/12 | chr12 | 102912772 | ||||||
| chr12:102913046
|
T | C | 1 | a0001c0001t0004g0232 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.61-148A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102913046 | ||||||
| chr12:102913158
|
C | T | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-260G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102913158 | ||||||
| chr12:102913243
|
A | G | 85 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(82): Show | 86 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.61-345T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102913243 | ||||||
| chr12:102913333
|
T | C | 1 | a0001c0001t0025g0234 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.61-435A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102913333 | ||||||
| chr12:102913408
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.61-510G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102913408 | ||||||
| chr12:102913545
|
A | C | 1 | a0001c0001t0001g0020 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.61-647T>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102913545 | ||||||
| chr12:102913583
|
G | A | 179 | a0001c0001t0001g0018a0001c0001t0001g0156a0001c0001t0001g0162others(176): Show | 182 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.61-685C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102913583 | ||||||
| chr12:102913623
|
A | G | 1 | a0001c0004t0026g0304 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.61-725T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102913623 | ||||||
| chr12:102913720
|
A | G | 1 | a0001c0010t0001g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.61-822T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102913720 | ||||||
| chr12:102913805
|
A | G | 50 | a0001c0001t0003g0255a0001c0001t0003g0271a0001c0001t0004g0262others(47): Show | 51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.61-907T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102913805 | ||||||
| chr12:102913918
|
C | T | 1 | a0001c0001t0025g0234 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.61-1020G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102913918 | ||||||
| chr12:102914057
|
A | G | 72 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(69): Show | 73 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.61-1159T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102914057 | ||||||
| chr12:102914260
|
TA | T | 3 | a0001c0003t0003g0243a0001c0003t0003g0244a0001c0003t0003g0245 | 3 | HG00597.hp2 HG02040.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.61-1363delT | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102914260 | ||||||
| chr12:102914271
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.61-1373T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102914271 | ||||||
| chr12:102914384
|
T | C | 1 | a0001c0004t0002g0150 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.61-1486A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102914384 | ||||||
| chr12:102914474
|
T | A | 54 | a0001c0001t0003g0255a0001c0001t0003g0271a0001c0001t0004g0262others(51): Show | 55 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.61-1576A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102914474 | ||||||
| chr12:102914604
|
GTCT | G | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG01074.hp1 HG01255.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-1709_61-1707del others(3): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102914604 | ||||||
| chr12:102914676
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.61-1778G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102914676 | ||||||
| chr12:102914865
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.61-1967G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102914865 | ||||||
| chr12:102914868
|
A | G | 145 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(142): Show | 147 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.61-1970T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102914868 | ||||||
| chr12:102915236
|
C | T | 12 | a0001c0001t0003g0233a0001c0001t0009g0298a0001c0001t0009g0299others(9): Show | 12 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.60+1835G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102915236 | ||||||
| chr12:102915312
|
T | C | 6 | a0001c0001t0004g0294a0001c0001t0004g0295a0001c0001t0004g0296others(3): Show | 6 | HG02258.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+1759A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102915312 | ||||||
| chr12:102915420
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.60+1651C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102915420 | ||||||
| chr12:102915420
|
G | T | 13 | a0001c0001t0001g0018a0001c0001t0002g0004a0001c0001t0002g0009others(10): Show | 14 | HG00741.hp1 HG01167.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.60+1651C>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102915420 | ||||||
| chr12:102915545
|
T | A | 11 | a0001c0001t0012g0146a0001c0004t0001g0140a0001c0004t0001g0141others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+1526A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102915545 | ||||||
| chr12:102915618
|
G | A | 145 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(142): Show | 147 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.60+1453C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102915618 | ||||||
| chr12:102915820
|
A | AT | 137 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(134): Show | 139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.60+1250dupA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102915820 | ||||||
| chr12:102915849
|
G | A | 4 | a0001c0004t0008g0300a0001c0004t0008g0301a0001c0004t0008g0302others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+1222C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102915849 | ||||||
| chr12:102915954
|
C | T | 66 | a0001c0001t0003g0233a0001c0001t0003g0255a0001c0001t0003g0271others(63): Show | 67 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.60+1117G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102915954 | ||||||
| chr12:102916012
|
C | T | 6 | a0001c0001t0009g0298a0001c0001t0009g0299a0001c0004t0008g0300others(3): Show | 6 | HG02451.hp1 HG02486.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+1059G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916012 | ||||||
| chr12:102916144
|
AT | A | 10 | a0001c0001t0002g0004a0001c0001t0002g0151a0001c0001t0002g0152others(7): Show | 11 | HG00741.hp1 HG01256.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.60+926delA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916144 | ||||||
| chr12:102916144
|
ATT | A | 138 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(135): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.60+925_60+926delAA | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916144 | ||||||
| chr12:102916167
|
T | A | 139 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0179others(136): Show | 141 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.60+904A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916167 | ||||||
| chr12:102916276
|
C | A | 1 | a0001c0001t0002g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.60+795G>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916276 | ||||||
| chr12:102916395
|
G | C | 66 | a0001c0001t0003g0233a0001c0001t0003g0255a0001c0001t0003g0271others(63): Show | 67 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.60+676C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916395 | ||||||
| chr12:102916442
|
G | A | 1 | a0001c0002t0001g0158 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.60+629C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916442 | ||||||
| chr12:102916560
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.60+511A>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916560 | ||||||
| chr12:102916663
|
G | A | 1 | a0001c0002t0001g0160 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.60+408C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916663 | ||||||
| chr12:102916739
|
A | G | 1 | a0001c0001t0002g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.60+332T>C | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916739 | ||||||
| chr12:102916753
|
T | A | 138 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(135): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.60+318A>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916753 | ||||||
| chr12:102916772
|
G | C | 3 | a0001c0001t0009g0305a0001c0001t0009g0306a0001c0004t0026g0304 | 3 | HG00639.hp1 HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.60+299C>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916772 | ||||||
| chr12:102916873
|
C | T | 1 | a0001c0002t0003g0231 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.60+198G>A | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916873 | ||||||
| chr12:102916895
|
T | TAGAAACA others(315): Show |
1 | a0001c0001t0006g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.60+175_60+176insTT others(320): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916895 | ||||||
| chr12:102916895
|
T | TAGAAACA others(316): Show |
2 | a0001c0001t0006g0227a0001c0008t0001g0228 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.60+175_60+176insTT others(321): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916895 | ||||||
| chr12:102916895
|
T | TAGAAACA others(319): Show |
2 | a0001c0001t0006g0229a0001c0001t0006g0230 | 2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.60+175_60+176insTT others(324): Show |
PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916895 | ||||||
| chr12:102916937
|
T | C | 138 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(135): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.60+134A>G | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102916937 | ||||||
| chr12:102917009
|
G | A | 147 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0184others(144): Show | 149 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.60+62C>T | PAH | ENSG00000171759.10 | transcript | ENST00000553106.6 | protein_coding | 1/12 | chr12 | 102917009 |