Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 763 |
|---|---|
| ensemblid | ENSG00000174990.8 |
| hgncid | 1377 |
| symbol | CA5A |
| name | carbonic anhydrase 5A |
| refseq_nuc | NM_001739.2 |
| refseq_prot | NP_001730.1 |
| ensembl_nuc | ENST00000649794.3 |
| ensembl_prot | ENSP00000498065.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 87888013 |
| end | 87936529 |
| strand | - |
| ver | v1.2 |
| region | chr16:87888013-87936529 |
| region5000 | chr16:87883013-87941529 |
| regionname0 | CA5A_chr16_87888013_87936529 |
| regionname5000 | CA5A_chr16_87883013_87941529 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 305 | 373 | 72 | 76 | 158 | 15 | 50 | 116 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0002 | 0/0 | 305 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0003 | 0/0 | 305 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0004 | 0/0 | 305 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0005 | 0/0 | 305 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0006 | 0/0 | 305 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 918 | 291 | 61 | 67 | 119 | 11 | 31 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0002 | 0/0 | 918 | 48 | 4 | 2 | 24 | 2 | 16 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0003 | 0/0 | 918 | 18 | 6 | 4 | 4 | 1 | 3 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0004 | 0/0 | 918 | 13 | 0 | 2 | 11 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0005 | 0/0 | 918 | 11 | 11 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0006 | 0/0 | 918 | 8 | 7 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0007 | 0/0 | 918 | 2 | 0 | 0 | 2 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0008 | 0/0 | 918 | 2 | 2 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0009 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0010 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0011 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0012 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0013 | 0/0 | 918 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0014 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| c0015 | 0/0 | 918 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 196 | 326 | 76 | 71 | 132 | 13 | 32 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| t0002 | 0/0 | 196 | 68 | 12 | 7 | 28 | 3 | 18 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| t0003 | 0/0 | 196 | 6 | 6 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| 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 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0212 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0298 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0391 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0397 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| g0398 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 918 | 291 | 61 | 67 | 119 | 11 | 31 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0002 | 0/0 | 918 | 48 | 4 | 2 | 24 | 2 | 16 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0003 | 0/0 | 918 | 18 | 6 | 4 | 4 | 1 | 3 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0004 | 0/0 | 918 | 13 | 0 | 2 | 11 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0012 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0013 | 0/0 | 918 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0014 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0002c0005 | 0/0 | 918 | 11 | 11 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0002c0010 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0002c0011 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0003c0006 | 0/0 | 918 | 8 | 7 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0003c0009 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0004c0007 | 0/0 | 918 | 2 | 0 | 0 | 2 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0005c0008 | 0/0 | 918 | 2 | 2 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0006c0015 | 0/0 | 918 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1113 | 286 | 56 | 67 | 119 | 11 | 31 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0001t0003 | 0/0 | 1113 | 5 | 5 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0002t0001 | 0/0 | 1113 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0002t0002 | 0/0 | 1113 | 47 | 4 | 2 | 24 | 2 | 15 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0003t0002 | 0/0 | 1113 | 18 | 6 | 4 | 4 | 1 | 3 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0004t0001 | 0/0 | 1113 | 13 | 0 | 2 | 11 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0012t0001 | 0/0 | 1113 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0013t0001 | 0/0 | 1113 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0001c0014t0001 | 0/0 | 1113 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0002c0005t0001 | 0/0 | 1113 | 10 | 10 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0002c0005t0003 | 0/0 | 1113 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0002c0010t0002 | 0/0 | 1113 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0002c0011t0002 | 0/0 | 1113 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0003c0006t0001 | 0/0 | 1113 | 8 | 7 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0003c0009t0002 | 0/0 | 1113 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0004c0007t0001 | 0/0 | 1113 | 2 | 0 | 0 | 2 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0005c0008t0001 | 0/0 | 1113 | 2 | 2 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| a0006c0015t0001 | 0/0 | 1113 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | copy fasta | chr16 | 87883013 | 87941529 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0212 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0298 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0001g0397 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0001t0003g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0391 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0002t0002g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0003t0002g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0004t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0004t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0004t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0004t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0004t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0004t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0012t0001g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0013t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0001c0014t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0002c0005t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0002c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0002c0005t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0002c0005t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0002c0005t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0002c0005t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0002c0005t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0002c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0002c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0002c0005t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0002c0005t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0002c0010t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0002c0011t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0003c0006t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0003c0006t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0003c0006t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0003c0006t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0003c0006t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0003c0006t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0003c0006t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0003c0006t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0003c0009t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0004c0007t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0004c0007t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0005c0008t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0005c0008t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| a0006c0015t0001g0398 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | GBR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0363 | EUR | FIN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00280 | hp2 | a0006 | c0015 | t0001 | g0398 | EUR | FIN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | FIN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0074 | EUR | FIN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0373 | EAS | CHS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | CHS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | CHS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00639 | hp2 | a0002 | c0011 | t0002 | g0019 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0324 | EAS | CHS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01069 | hp2 | a0001 | c0003 | t0002 | g0115 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0075 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0368 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01168 | hp1 | a0001 | c0003 | t0002 | g0185 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0374 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0397 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01192 | hp2 | a0001 | c0004 | t0001 | g0367 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01243 | hp1 | a0003 | c0006 | t0001 | g0004 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0033 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0366 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01358 | hp2 | a0001 | c0003 | t0002 | g0332 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0350 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01433 | hp2 | a0001 | c0014 | t0001 | g0102 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01515 | hp1 | a0001 | c0013 | t0001 | g0321 | EUR | IBS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0032 | EUR | IBS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0219 | EUR | IBS | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01891 | hp2 | a0001 | c0003 | t0002 | g0041 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01952 | hp1 | a0001 | c0004 | t0001 | g0369 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0393 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0259 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0382 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0331 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02083 | hp2 | a0001 | c0004 | t0001 | g0151 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02132 | hp1 | a0001 | c0004 | t0001 | g0338 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0343 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02145 | hp1 | a0003 | c0006 | t0001 | g0011 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CDX | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | CDX | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | CDX | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02258 | hp1 | a0002 | c0005 | t0001 | g0012 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02258 | hp2 | a0003 | c0006 | t0001 | g0009 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0378 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0375 | AMR | PEL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02523 | hp2 | a0001 | c0004 | t0001 | g0323 | EAS | KHV | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0248 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02615 | hp2 | a0002 | c0005 | t0001 | g0023 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0087 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0380 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0386 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02630 | hp2 | a0002 | c0005 | t0001 | g0021 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02647 | hp1 | a0003 | c0006 | t0001 | g0003 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0253 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0285 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02717 | hp2 | a0002 | c0005 | t0001 | g0024 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0286 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02738 | hp2 | a0001 | c0003 | t0002 | g0090 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0232 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02886 | hp2 | a0002 | c0005 | t0001 | g0022 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02896 | hp1 | a0003 | c0006 | t0001 | g0010 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02896 | hp2 | a0003 | c0006 | t0001 | g0005 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02897 | hp1 | a0003 | c0006 | t0001 | g0006 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02965 | hp2 | a0001 | c0003 | t0002 | g0067 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02970 | hp2 | a0003 | c0006 | t0001 | g0007 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0384 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0181 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03098 | hp2 | a0002 | c0005 | t0003 | g0020 | AFR | MSL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03139 | hp2 | a0003 | c0009 | t0002 | g0008 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03195 | hp2 | a0002 | c0005 | t0001 | g0017 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03209 | hp1 | a0005 | c0008 | t0001 | g0050 | AFR | MSL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0270 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03453 | hp1 | a0002 | c0005 | t0001 | g0013 | AFR | MSL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03453 | hp2 | a0002 | c0010 | t0002 | g0018 | AFR | MSL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0076 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03491 | hp2 | a0001 | c0003 | t0002 | g0355 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0073 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0377 | AFR | ESN | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | GWD | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0381 | AFR | MSL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03579 | hp2 | a0005 | c0008 | t0001 | g0052 | AFR | MSL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0296 | SAS | STU | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0308 | SAS | STU | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0187 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0113 | SAS | PJL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0391 | SAS | BEB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | BEB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0333 | SAS | BEB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0387 | SAS | STU | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0261 | SAS | STU | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0354 | SAS | BEB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0177 | SAS | STU | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0249 | SAS | STU | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0376 | SAS | STU | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0383 | AFR | YRI | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | CHB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | YRI | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0385 | AFR | YRI | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0156 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0392 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18964 | hp2 | a0001 | c0004 | t0001 | g0133 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0390 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18967 | hp2 | a0001 | c0004 | t0001 | g0274 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18981 | hp2 | a0001 | c0003 | t0002 | g0183 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18983 | hp2 | a0001 | c0003 | t0002 | g0257 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18986 | hp2 | a0004 | c0007 | t0001 | g0170 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0394 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0396 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19011 | hp2 | a0001 | c0004 | t0001 | g0279 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19012 | hp1 | a0001 | c0004 | t0001 | g0255 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | LWK | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0379 | AFR | LWK | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19043 | hp1 | a0002 | c0005 | t0001 | g0015 | AFR | LWK | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0054 | AFR | LWK | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0395 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0034 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0337 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19076 | hp2 | a0001 | c0004 | t0001 | g0357 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19077 | hp2 | a0001 | c0004 | t0001 | g0131 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19080 | hp2 | a0001 | c0003 | t0002 | g0086 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19085 | hp2 | a0004 | c0007 | t0001 | g0107 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ASW | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ASW | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | TSI | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | GIH | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | GIH | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02486 | hp1 | a0002 | c0005 | t0001 | g0014 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG03471 | hp2 | a0001 | c0012 | t0001 | g0388 | AFR | MSL | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | USA | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | USA | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | USA | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA21309 | hp1 | a0002 | c0005 | t0001 | g0016 | AFR | LWK | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0298 | REF | REF | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0212 | REF | REF | CA5A_chr16_87883013_87941529 | CA5A | chr16 | 87883013 | 87941529 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:87891918
|
T | C | 1 | a0005 | 2 | HG03209.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.655A>G | p.Thr219Ala | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/7 | 734/1113 | 655/918 | 219/305 | chr16 | 87891918 | ||
| chr16:87902436
|
C | T | 1 | a0004 | 2 | NA18986.hp2 NA19085.hp2 |
missense_variant | MODERATE | c.544G>A | p.Val182Met | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 4/7 | 623/1113 | 544/918 | 182/305 | chr16 | 87902436 | ||
| chr16:87936313
|
G | T | 1 | a0002 | 13 | HG00639.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
missense_variant | MODERATE | c.138C>A | p.Asn46Lys | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/7 | 217/1113 | 138/918 | 46/305 | chr16 | 87936313 | ||
| chr16:87936316
|
A | T | 1 | a0003 | 9 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
missense_variant | MODERATE | c.135T>A | p.Asn45Lys | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/7 | 214/1113 | 135/918 | 45/305 | chr16 | 87936316 | ||
| chr16:87936371
|
G | C | 1 | a0006 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.80C>G | p.Ser27Trp | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/7 | 159/1113 | 80/918 | 27/305 | chr16 | 87936371 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:87888165
|
C | T | 1 | a0005c0008 | 2 | HG03209.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.882G>A | p.Ala294Ala | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 7/7 | 961/1113 | 882/918 | 294/305 | chr16 | 87888165 | ||
| chr16:87888240
|
T | A | 5 | a0001c0002a0001c0003a0002c0010others(2): Show | 69 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(66): Show |
synonymous_variant | LOW | c.807A>T | p.Ala269Ala | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 7/7 | 886/1113 | 807/918 | 269/305 | chr16 | 87888240 | ||
| chr16:87891928
|
G | A | 2 | a0001c0013a0001c0014 | 2 | HG01433.hp2 HG01515.hp1 |
synonymous_variant | LOW | c.645C>T | p.Phe215Phe | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/7 | 724/1113 | 645/918 | 215/305 | chr16 | 87891928 | ||
| chr16:87901927
|
C | T | 1 | a0001c0012 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.603G>A | p.Pro201Pro | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/7 | 682/1113 | 603/918 | 201/305 | chr16 | 87901927 | ||
| chr16:87904792
|
G | A | 5 | a0001c0002a0001c0004a0001c0014others(2): Show | 64 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(61): Show |
synonymous_variant | LOW | c.453C>T | p.Pro151Pro | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/7 | 532/1113 | 453/918 | 151/305 | chr16 | 87904792 | ||
| chr16:87926874
|
T | G | 1 | a0001c0014 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.214A>C | p.Arg72Arg | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/7 | 293/1113 | 214/918 | 72/305 | chr16 | 87926874 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:87888048
|
G | A | 5 | a0001c0002t0002a0001c0003t0002a0002c0010t0002others(2): Show | 68 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*81C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 7/7 | 81 | chr16 | 87888048 | |||||
| chr16:87888079
|
C | T | 2 | a0001c0001t0003a0002c0005t0003 | 6 | HG01884.hp2 HG02280.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*50G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 7/7 | 50 | chr16 | 87888079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:87888311
|
G | A | 6 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-39C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888311 | ||||||
| chr16:87888328
|
C | T | 5 | a0001c0001t0001g0167a0001c0001t0001g0283a0001c0001t0001g0314others(2): Show | 5 | HG02027.hp2 HG02071.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-56G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888328 | ||||||
| chr16:87888329
|
T | C | 69 | a0001c0002t0001g0249a0001c0002t0002g0032a0001c0002t0002g0033others(66): Show | 69 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.775-57A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888329 | ||||||
| chr16:87888417
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.775-145A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888417 | ||||||
| chr16:87888425
|
G | C | 2 | a0001c0002t0002g0308a0001c0002t0002g0387 | 2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.775-153C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888425 | ||||||
| chr16:87888430
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0040others(124): Show | 128 | HG00323.hp2 HG00438.hp2 HG00621.hp2 others(125): Show |
intron_variant | MODIFIER | c.775-158T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888430 | ||||||
| chr16:87888454
|
G | A | 69 | a0001c0002t0001g0249a0001c0002t0002g0032a0001c0002t0002g0033others(66): Show | 69 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.775-182C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888454 | ||||||
| chr16:87888468
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0315a0001c0001t0001g0373 | 3 | HG00438.hp1 HG02040.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.775-196C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888468 | ||||||
| chr16:87888515
|
C | G | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.775-243G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888515 | ||||||
| chr16:87888557
|
C | T | 68 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0073others(65): Show | 68 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.775-285G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888557 | ||||||
| chr16:87888565
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.775-293C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888565 | ||||||
| chr16:87888674
|
C | T | 1 | a0001c0002t0002g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.775-402G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888674 | ||||||
| chr16:87888690
|
G | A | 19 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(16): Show | 19 | HG02145.hp2 HG02572.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.775-418C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888690 | ||||||
| chr16:87888757
|
T | A | 12 | a0001c0001t0001g0048a0001c0001t0001g0096a0001c0001t0001g0189others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.775-485A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888757 | ||||||
| chr16:87888827
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.775-555C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888827 | ||||||
| chr16:87888850
|
T | G | 5 | a0001c0003t0002g0041a0001c0003t0002g0054a0001c0003t0002g0379others(2): Show | 5 | HG01891.hp2 HG03579.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-578A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888850 | ||||||
| chr16:87888869
|
C | T | 2 | a0001c0013t0001g0321a0001c0014t0001g0102 | 2 | HG01433.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.775-597G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888869 | ||||||
| chr16:87888878
|
G | A | 13 | a0001c0001t0001g0048a0001c0001t0001g0096a0001c0001t0001g0189others(10): Show | 13 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.775-606C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888878 | ||||||
| chr16:87888919
|
A | AT | 76 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0077others(73): Show | 76 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.775-648dupA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888919 | ||||||
| chr16:87888965
|
A | C | 69 | a0001c0002t0001g0249a0001c0002t0002g0032a0001c0002t0002g0033others(66): Show | 69 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.775-693T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888965 | ||||||
| chr16:87888997
|
G | A | 30 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0059others(27): Show | 30 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.775-725C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87888997 | ||||||
| chr16:87889005
|
T | C | 88 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(85): Show | 88 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.775-733A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889005 | ||||||
| chr16:87889110
|
G | C | 1 | a0001c0004t0001g0323 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.775-838C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889110 | ||||||
| chr16:87889198
|
C | T | 1 | a0001c0003t0002g0086 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.775-926G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889198 | ||||||
| chr16:87889218
|
C | A | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.775-946G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889218 | ||||||
| chr16:87889256
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.775-984A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889256 | ||||||
| chr16:87889349
|
C | T | 2 | a0005c0008t0001g0050a0005c0008t0001g0052 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.775-1077G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889349 | ||||||
| chr16:87889353
|
T | C | 146 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0038others(143): Show | 146 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(143): Show |
intron_variant | MODIFIER | c.775-1081A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889353 | ||||||
| chr16:87889361
|
T | C | 7 | a0001c0001t0001g0060a0001c0001t0001g0359a0002c0005t0001g0022others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-1089A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889361 | ||||||
| chr16:87889472
|
A | T | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.775-1200T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889472 | ||||||
| chr16:87889544
|
T | C | 1 | a0003c0006t0001g0004 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.775-1272A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889544 | ||||||
| chr16:87889553
|
C | T | 69 | a0001c0002t0001g0249a0001c0002t0002g0032a0001c0002t0002g0033others(66): Show | 69 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.775-1281G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889553 | ||||||
| chr16:87889591
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.775-1319A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889591 | ||||||
| chr16:87889736
|
A | G | 69 | a0001c0002t0001g0249a0001c0002t0002g0032a0001c0002t0002g0033others(66): Show | 69 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.775-1464T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889736 | ||||||
| chr16:87889749
|
C | G | 8 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.775-1477G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889749 | ||||||
| chr16:87889752
|
G | C | 124 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(121): Show | 124 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.775-1480C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889752 | ||||||
| chr16:87889846
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.775-1574A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889846 | ||||||
| chr16:87889854
|
G | A | 64 | a0001c0002t0001g0249a0001c0002t0002g0032a0001c0002t0002g0033others(61): Show | 64 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.775-1582C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889854 | ||||||
| chr16:87889879
|
C | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.775-1607G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889879 | ||||||
| chr16:87889914
|
C | G | 3 | a0001c0001t0001g0359a0002c0005t0001g0022a0003c0006t0001g0009 | 3 | HG01109.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.775-1642G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889914 | ||||||
| chr16:87889949
|
C | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.775-1677G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889949 | ||||||
| chr16:87889959
|
A | G | 13 | a0001c0001t0001g0048a0001c0001t0001g0096a0001c0001t0001g0189others(10): Show | 13 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.775-1687T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889959 | ||||||
| chr16:87889966
|
C | T | 1 | a0001c0003t0002g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.775-1694G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87889966 | ||||||
| chr16:87890036
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.774+1763A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890036 | ||||||
| chr16:87890077
|
C | T | 1 | a0001c0003t0002g0355 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.774+1722G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890077 | ||||||
| chr16:87890176
|
C | A | 2 | a0001c0002t0002g0308a0001c0002t0002g0387 | 2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.774+1623G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890176 | ||||||
| chr16:87890197
|
A | G | 1 | a0001c0001t0001g0360 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.774+1602T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890197 | ||||||
| chr16:87890267
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.774+1532G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890267 | ||||||
| chr16:87890302
|
AC | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+1496delG | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890302 | ||||||
| chr16:87890320
|
T | C | 8 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+1479A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890320 | ||||||
| chr16:87890474
|
C | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0268 | 2 | NA18942.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.774+1325G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890474 | ||||||
| chr16:87890504
|
C | CG | 6 | a0001c0001t0001g0078a0001c0001t0001g0203a0001c0001t0001g0236others(3): Show | 6 | HG00438.hp2 HG01978.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.774+1294dupC | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890504 | ||||||
| chr16:87890637
|
G | A | 69 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0073others(66): Show | 69 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.774+1162C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890637 | ||||||
| chr16:87890676
|
T | C | 12 | a0001c0001t0001g0048a0001c0001t0001g0096a0001c0001t0001g0189others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.774+1123A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890676 | ||||||
| chr16:87890762
|
A | C | 385 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(382): Show | 387 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(384): Show |
intron_variant | MODIFIER | c.774+1037T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890762 | ||||||
| chr16:87890764
|
C | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0182a0001c0001t0001g0231others(1): Show | 4 | HG01081.hp1 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+1035G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890764 | ||||||
| chr16:87890779
|
C | G | 1 | a0001c0001t0001g0366 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.774+1020G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890779 | ||||||
| chr16:87890888
|
G | A | 7 | a0001c0001t0001g0069a0001c0001t0001g0114a0001c0001t0001g0117others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.774+911C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890888 | ||||||
| chr16:87890891
|
T | C | 15 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.774+908A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890891 | ||||||
| chr16:87890983
|
G | C | 70 | a0001c0002t0001g0249a0001c0002t0002g0032a0001c0002t0002g0033others(67): Show | 70 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.774+816C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890983 | ||||||
| chr16:87890985
|
G | A | 5 | a0001c0004t0001g0034a0001c0004t0001g0131a0001c0004t0001g0274others(2): Show | 5 | NA18967.hp2 NA19011.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+814C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87890985 | ||||||
| chr16:87891014
|
G | C | 1 | a0001c0001t0001g0307 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.774+785C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891014 | ||||||
| chr16:87891021
|
T | C | 11 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(8): Show | 11 | HG02630.hp2 HG02723.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.774+778A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891021 | ||||||
| chr16:87891038
|
G | C | 86 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(83): Show | 86 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.774+761C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891038 | ||||||
| chr16:87891118
|
A | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0066a0001c0001t0001g0068others(5): Show | 8 | HG01167.hp1 HG01243.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+681T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891118 | ||||||
| chr16:87891134
|
T | C | 70 | a0001c0002t0001g0249a0001c0002t0002g0032a0001c0002t0002g0033others(67): Show | 70 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.774+665A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891134 | ||||||
| chr16:87891137
|
A | C | 1 | a0001c0004t0001g0255 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.774+662T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891137 | ||||||
| chr16:87891143
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.774+656C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891143 | ||||||
| chr16:87891143
|
GA | G | 100 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(97): Show | 100 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.774+655delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891143 | ||||||
| chr16:87891143
|
GAA | G | 7 | a0001c0001t0001g0077a0001c0001t0003g0049a0001c0001t0003g0065others(4): Show | 7 | HG01884.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.774+654_774+655del others(2): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891143 | ||||||
| chr16:87891220
|
C | T | 1 | a0001c0002t0002g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.774+579G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891220 | ||||||
| chr16:87891221
|
G | A | 1 | a0001c0003t0002g0183 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.774+578C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891221 | ||||||
| chr16:87891261
|
A | C | 1 | a0001c0001t0001g0207 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.774+538T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891261 | ||||||
| chr16:87891323
|
C | G | 4 | a0001c0003t0002g0041a0001c0003t0002g0054a0001c0003t0002g0379others(1): Show | 4 | HG01891.hp2 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+476G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891323 | ||||||
| chr16:87891332
|
G | C | 15 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.774+467C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891332 | ||||||
| chr16:87891342
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.774+457G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891342 | ||||||
| chr16:87891383
|
G | A | 1 | a0002c0005t0001g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.774+416C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891383 | ||||||
| chr16:87891416
|
C | T | 3 | a0001c0002t0002g0157a0001c0002t0002g0295a0001c0003t0002g0257 | 3 | NA18979.hp2 NA18983.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.774+383G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891416 | ||||||
| chr16:87891417
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.774+382C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891417 | ||||||
| chr16:87891422
|
C | T | 2 | a0001c0001t0001g0063a0001c0012t0001g0388 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.774+377G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891422 | ||||||
| chr16:87891423
|
G | A | 4 | a0001c0001t0001g0053a0001c0001t0001g0227a0001c0001t0001g0265others(1): Show | 4 | NA18943.hp2 NA18956.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+376C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891423 | ||||||
| chr16:87891467
|
C | CA | 71 | a0001c0002t0001g0249a0001c0002t0002g0032a0001c0002t0002g0033others(68): Show | 71 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.774+331dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891467 | ||||||
| chr16:87891514
|
T | C | 4 | a0001c0001t0001g0047a0001c0001t0001g0182a0001c0001t0001g0231others(1): Show | 4 | HG01081.hp1 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+285A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891514 | ||||||
| chr16:87891649
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.774+150A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891649 | ||||||
| chr16:87891654
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.774+145A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891654 | ||||||
| chr16:87891654
|
T | C | 127 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(124): Show | 127 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(124): Show |
intron_variant | MODIFIER | c.774+145A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891654 | ||||||
| chr16:87891673
|
T | G | 73 | a0001c0001t0001g0069a0001c0001t0001g0127a0001c0001t0001g0335others(70): Show | 73 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.774+126A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891673 | ||||||
| chr16:87891764
|
G | A | 5 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0003g0230others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+35C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 6/6 | chr16 | 87891764 | ||||||
| chr16:87892149
|
G | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.619-195C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892149 | ||||||
| chr16:87892206
|
A | G | 72 | a0001c0001t0001g0069a0001c0001t0001g0127a0001c0001t0001g0335others(69): Show | 72 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.619-252T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892206 | ||||||
| chr16:87892281
|
G | A | 2 | a0005c0008t0001g0050a0005c0008t0001g0052 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.619-327C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892281 | ||||||
| chr16:87892355
|
C | G | 30 | a0001c0001t0001g0047a0001c0001t0001g0059a0001c0001t0001g0061others(27): Show | 30 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.619-401G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892355 | ||||||
| chr16:87892400
|
C | G | 13 | a0001c0001t0001g0048a0001c0001t0001g0096a0001c0001t0001g0189others(10): Show | 13 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.619-446G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892400 | ||||||
| chr16:87892433
|
C | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0071 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.619-479G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892433 | ||||||
| chr16:87892510
|
A | AAAT | 25 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0080others(22): Show | 26 | HG00438.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.619-559_619-557dup others(3): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892510 | ||||||
| chr16:87892510
|
A | AAATAAT | 9 | a0001c0001t0001g0093a0001c0001t0001g0147a0001c0001t0001g0210others(6): Show | 9 | HG00280.hp2 HG00408.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.619-562_619-557dup others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892510 | ||||||
| chr16:87892510
|
A | AAATAATA others(2): Show |
3 | a0001c0001t0001g0214a0001c0001t0001g0292a0001c0004t0001g0255 | 3 | NA18961.hp1 NA18978.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.619-565_619-557dup others(9): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892510 | ||||||
| chr16:87892510
|
AAAT | A | 56 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0066others(53): Show | 56 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.619-559_619-557del others(3): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892510 | ||||||
| chr16:87892510
|
AAATAAT | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0055others(24): Show | 28 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.619-562_619-557del others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892510 | ||||||
| chr16:87892510
|
AAATAATA others(2): Show |
A | 14 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0068others(11): Show | 14 | HG00741.hp1 HG01346.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.619-565_619-557del others(9): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892510 | ||||||
| chr16:87892510
|
AAATAATA others(5): Show |
A | 9 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0042others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.619-568_619-557del others(12): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892510 | ||||||
| chr16:87892510
|
AAATAATA others(8): Show |
A | 12 | a0001c0001t0001g0048a0001c0001t0001g0096a0001c0001t0001g0189others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.619-571_619-557del others(15): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892510 | ||||||
| chr16:87892510
|
AAATAATA others(11): Show |
A | 10 | a0001c0001t0001g0059a0001c0001t0001g0077a0001c0001t0001g0116others(7): Show | 10 | HG00639.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-574_619-557del others(18): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892510 | ||||||
| chr16:87892510
|
AAATAATA others(14): Show |
A | 36 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(33): Show | 36 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.619-577_619-557del others(21): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892510 | ||||||
| chr16:87892544
|
AATAATAA others(9): Show |
A | 1 | a0001c0003t0002g0219 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.619-606_619-591del others(16): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892544 | ||||||
| chr16:87892547
|
AATAATAA others(6): Show |
A | 1 | a0002c0010t0002g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.619-606_619-594del others(13): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892547 | ||||||
| chr16:87892550
|
AATAATAA others(3): Show |
A | 1 | a0001c0002t0002g0241 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.619-606_619-597del others(10): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892550 | ||||||
| chr16:87892553
|
AATAAATT | A | 9 | a0001c0001t0001g0275a0001c0002t0002g0232a0001c0002t0002g0247others(6): Show | 9 | HG02683.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.619-606_619-600del others(7): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892553 | ||||||
| chr16:87892555
|
TA | T | 16 | a0001c0002t0001g0249a0001c0002t0002g0073a0001c0002t0002g0076others(13): Show | 16 | HG00438.hp2 HG00673.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.619-602delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892555 | ||||||
| chr16:87892556
|
A | AAT | 10 | a0001c0002t0002g0148a0001c0002t0002g0204a0001c0002t0002g0218others(7): Show | 10 | HG02056.hp1 HG02083.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-603_619-602ins others(2): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892556 | ||||||
| chr16:87892556
|
A | AATAAT | 3 | a0001c0002t0002g0157a0001c0002t0002g0213a0001c0003t0002g0257 | 3 | HG02165.hp1 NA18983.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.619-603_619-602ins others(5): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892556 | ||||||
| chr16:87892556
|
A | T | 2 | a0005c0008t0001g0050a0005c0008t0001g0052 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.619-602T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892556 | ||||||
| chr16:87892556
|
AAATT | A | 30 | a0001c0001t0001g0202a0001c0002t0002g0032a0001c0002t0002g0033others(27): Show | 30 | HG00323.hp2 HG00639.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.619-606_619-603del others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892556 | ||||||
| chr16:87892560
|
T | A | 29 | a0001c0002t0001g0249a0001c0002t0002g0073a0001c0002t0002g0076others(26): Show | 29 | HG00438.hp2 HG00673.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.619-606A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892560 | ||||||
| chr16:87892673
|
C | CT | 7 | a0001c0001t0001g0029a0001c0001t0001g0084a0001c0001t0001g0200others(4): Show | 7 | HG02293.hp2 HG03209.hp1 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.619-720dupA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892673 | ||||||
| chr16:87892673
|
CT | C | 113 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0051others(110): Show | 113 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.619-720delA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892673 | ||||||
| chr16:87892673
|
CTT | C | 9 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(6): Show | 9 | HG01070.hp1 HG02145.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.619-721_619-720del others(2): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892673 | ||||||
| chr16:87892691
|
G | A | 1 | a0001c0001t0001g0366 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.619-737C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892691 | ||||||
| chr16:87892692
|
A | T | 1 | a0001c0001t0001g0366 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.619-738T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892692 | ||||||
| chr16:87892695
|
T | A | 15 | a0001c0001t0001g0059a0001c0001t0001g0069a0001c0001t0001g0077others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.619-741A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892695 | ||||||
| chr16:87892889
|
C | T | 1 | a0001c0004t0001g0357 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.619-935G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892889 | ||||||
| chr16:87892901
|
C | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0359a0002c0005t0001g0022others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-947G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892901 | ||||||
| chr16:87892949
|
T | C | 13 | a0001c0001t0001g0048a0001c0001t0001g0096a0001c0001t0001g0189others(10): Show | 13 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.619-995A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892949 | ||||||
| chr16:87892952
|
G | A | 96 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0064others(93): Show | 96 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.619-998C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892952 | ||||||
| chr16:87892992
|
G | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.619-1038C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87892992 | ||||||
| chr16:87893020
|
C | A | 1 | a0001c0001t0001g0202 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.619-1066G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893020 | ||||||
| chr16:87893083
|
G | T | 1 | a0001c0003t0002g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.619-1129C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893083 | ||||||
| chr16:87893090
|
G | C | 101 | a0001c0001t0001g0047a0001c0001t0001g0059a0001c0001t0001g0061others(98): Show | 101 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.619-1136C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893090 | ||||||
| chr16:87893125
|
C | CCTTT | 15 | a0001c0001t0001g0048a0001c0001t0001g0096a0001c0001t0001g0189others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.619-1175_619-1172d others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893125 | ||||||
| chr16:87893125
|
C | CCTTTCTT others(5): Show |
1 | a0001c0001t0001g0060 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.619-1183_619-1172d others(14): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893125 | ||||||
| chr16:87893125
|
CCTTT | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0231a0001c0001t0001g0291 | 3 | HG01081.hp1 HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.619-1175_619-1172d others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893125 | ||||||
| chr16:87893132
|
T | G | 8 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.619-1178A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893132 | ||||||
| chr16:87893146
|
C | T | 85 | a0001c0001t0001g0059a0001c0001t0001g0069a0001c0001t0001g0077others(82): Show | 85 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.619-1192G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893146 | ||||||
| chr16:87893230
|
C | T | 10 | a0001c0001t0001g0069a0001c0001t0001g0114a0001c0001t0001g0117others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.619-1276G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893230 | ||||||
| chr16:87893250
|
C | G | 8 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0073others(5): Show | 8 | HG00323.hp2 HG01257.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.619-1296G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893250 | ||||||
| chr16:87893276
|
C | A | 1 | a0001c0002t0002g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.619-1322G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893276 | ||||||
| chr16:87893359
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.619-1405G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893359 | ||||||
| chr16:87893360
|
C | T | 1 | a0001c0001t0001g0375 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.619-1406G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893360 | ||||||
| chr16:87893388
|
A | C | 3 | a0001c0001t0001g0121a0001c0001t0001g0361a0002c0005t0001g0013 | 3 | HG02647.hp2 HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.619-1434T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893388 | ||||||
| chr16:87893411
|
G | A | 12 | a0001c0001t0001g0048a0001c0001t0001g0096a0001c0001t0001g0189others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.619-1457C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893411 | ||||||
| chr16:87893417
|
A | G | 12 | a0001c0001t0001g0048a0001c0001t0001g0096a0001c0001t0001g0189others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.619-1463T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893417 | ||||||
| chr16:87893554
|
C | T | 2 | a0001c0013t0001g0321a0001c0014t0001g0102 | 2 | HG01433.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.619-1600G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893554 | ||||||
| chr16:87893616
|
T | C | 90 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(87): Show | 90 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.619-1662A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893616 | ||||||
| chr16:87893651
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.619-1697G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893651 | ||||||
| chr16:87893684
|
C | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0165 | 2 | NA18977.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.619-1730G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893684 | ||||||
| chr16:87893685
|
G | A | 12 | a0001c0001t0001g0059a0001c0001t0001g0077a0001c0001t0001g0114others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.619-1731C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893685 | ||||||
| chr16:87893761
|
T | C | 1 | a0003c0006t0001g0011 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.619-1807A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893761 | ||||||
| chr16:87893855
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0003g0288 | 2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.619-1901G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893855 | ||||||
| chr16:87893912
|
C | G | 8 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.619-1958G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87893912 | ||||||
| chr16:87894090
|
G | A | 4 | a0001c0001t0001g0062a0001c0001t0001g0109a0001c0001t0001g0111others(1): Show | 4 | HG00099.hp1 HG00323.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-2136C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894090 | ||||||
| chr16:87894198
|
A | G | 89 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(86): Show | 89 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.619-2244T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894198 | ||||||
| chr16:87894310
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.619-2356T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894310 | ||||||
| chr16:87894479
|
G | C | 15 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0064others(12): Show | 15 | HG01081.hp1 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.619-2525C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894479 | ||||||
| chr16:87894551
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.619-2597G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894551 | ||||||
| chr16:87894573
|
T | TA | 20 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0064others(17): Show | 20 | HG01109.hp2 HG01346.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.619-2620dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894573 | ||||||
| chr16:87894573
|
TA | T | 84 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(81): Show | 84 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.619-2620delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894573 | ||||||
| chr16:87894594
|
A | G | 2 | a0005c0008t0001g0050a0005c0008t0001g0052 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.619-2640T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894594 | ||||||
| chr16:87894633
|
T | C | 79 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(76): Show | 79 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.619-2679A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894633 | ||||||
| chr16:87894665
|
A | T | 11 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(8): Show | 11 | HG02630.hp2 HG02723.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.619-2711T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894665 | ||||||
| chr16:87894700
|
G | C | 2 | a0001c0002t0002g0157a0001c0003t0002g0257 | 2 | NA18983.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.619-2746C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894700 | ||||||
| chr16:87894750
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.619-2796C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894750 | ||||||
| chr16:87894860
|
C | G | 1 | a0001c0001t0001g0167 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.619-2906G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894860 | ||||||
| chr16:87894860
|
CAG | C | 46 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0059others(43): Show | 46 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.619-2908_619-2907d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894860 | ||||||
| chr16:87894978
|
A | G | 90 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(87): Show | 90 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.619-3024T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87894978 | ||||||
| chr16:87895122
|
C | T | 12 | a0001c0001t0001g0048a0001c0001t0001g0189a0001c0001t0001g0190others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.619-3168G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895122 | ||||||
| chr16:87895145
|
G | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0359a0002c0005t0001g0022others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-3191C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895145 | ||||||
| chr16:87895267
|
T | C | 76 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(73): Show | 76 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.619-3313A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895267 | ||||||
| chr16:87895302
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.619-3348A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895302 | ||||||
| chr16:87895311
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.619-3357G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895311 | ||||||
| chr16:87895357
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.619-3403G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895357 | ||||||
| chr16:87895374
|
T | C | 88 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(85): Show | 88 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.619-3420A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895374 | ||||||
| chr16:87895551
|
GAAAACAA | G | 13 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(10): Show | 13 | HG02630.hp2 HG02723.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.619-3604_619-3598d others(9): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895551 | ||||||
| chr16:87895594
|
G | A | 8 | a0001c0001t0001g0059a0001c0001t0001g0077a0001c0001t0003g0049others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.619-3640C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895594 | ||||||
| chr16:87895607
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.619-3653A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895607 | ||||||
| chr16:87895622
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0001g0378 | 2 | HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.619-3668A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895622 | ||||||
| chr16:87895660
|
T | C | 2 | a0001c0002t0001g0249a0001c0004t0001g0323 | 2 | HG02523.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.619-3706A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895660 | ||||||
| chr16:87895712
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.619-3758G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895712 | ||||||
| chr16:87895762
|
G | A | 65 | a0001c0001t0001g0060a0001c0001t0001g0202a0001c0001t0001g0311others(62): Show | 65 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.619-3808C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895762 | ||||||
| chr16:87895767
|
A | C | 1 | a0001c0001t0001g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.619-3813T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895767 | ||||||
| chr16:87895966
|
C | T | 68 | a0001c0001t0001g0202a0001c0002t0001g0249a0001c0002t0002g0032others(65): Show | 68 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.619-4012G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895966 | ||||||
| chr16:87895990
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.619-4036C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895990 | ||||||
| chr16:87895994
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.619-4040C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87895994 | ||||||
| chr16:87896228
|
C | T | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | NA19080.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.619-4274G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896228 | ||||||
| chr16:87896280
|
A | T | 8 | a0001c0001t0001g0088a0001c0001t0001g0122a0001c0001t0001g0154others(5): Show | 8 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.619-4326T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896280 | ||||||
| chr16:87896289
|
C | A | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.619-4335G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896289 | ||||||
| chr16:87896289
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.619-4335G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896289 | ||||||
| chr16:87896359
|
G | C | 1 | a0001c0001t0001g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.619-4405C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896359 | ||||||
| chr16:87896397
|
G | C | 1 | a0001c0001t0001g0202 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.619-4443C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896397 | ||||||
| chr16:87896424
|
A | G | 11 | a0001c0001t0001g0047a0001c0001t0001g0059a0001c0001t0001g0182others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.619-4470T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896424 | ||||||
| chr16:87896509
|
C | G | 12 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(9): Show | 12 | HG02630.hp2 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.619-4555G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896509 | ||||||
| chr16:87896530
|
C | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-4576G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896530 | ||||||
| chr16:87896545
|
T | C | 2 | a0005c0008t0001g0050a0005c0008t0001g0052 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.619-4591A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896545 | ||||||
| chr16:87896591
|
C | A | 2 | a0001c0001t0001g0200a0003c0006t0001g0004 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.619-4637G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896591 | ||||||
| chr16:87896649
|
A | AT | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-4696dupA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896649 | ||||||
| chr16:87896652
|
G | T | 123 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(120): Show | 123 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.619-4698C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896652 | ||||||
| chr16:87896690
|
G | C | 4 | a0001c0001t0001g0060a0001c0001t0001g0359a0002c0005t0001g0022others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-4736C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896690 | ||||||
| chr16:87896757
|
T | C | 5 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0003g0230others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.619-4803A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896757 | ||||||
| chr16:87896854
|
C | T | 9 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(6): Show | 9 | HG02630.hp2 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.619-4900G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896854 | ||||||
| chr16:87896874
|
A | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0236 | 2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.619-4920T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896874 | ||||||
| chr16:87896920
|
G | T | 5 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0003g0230others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.619-4966C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896920 | ||||||
| chr16:87896981
|
G | A | 106 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(103): Show | 106 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.618+4931C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896981 | ||||||
| chr16:87896993
|
C | T | 2 | a0005c0008t0001g0050a0005c0008t0001g0052 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.618+4919G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87896993 | ||||||
| chr16:87897017
|
C | G | 2 | a0005c0008t0001g0050a0005c0008t0001g0052 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.618+4895G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897017 | ||||||
| chr16:87897072
|
G | A | 1 | a0001c0004t0001g0367 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.618+4840C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897072 | ||||||
| chr16:87897073
|
G | C | 5 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0003g0230others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+4839C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897073 | ||||||
| chr16:87897089
|
A | C | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.618+4823T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897089 | ||||||
| chr16:87897101
|
G | A | 11 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(8): Show | 11 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.618+4811C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897101 | ||||||
| chr16:87897116
|
A | G | 22 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.618+4796T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897116 | ||||||
| chr16:87897154
|
C | T | 14 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0064others(11): Show | 14 | HG01109.hp2 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.618+4758G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897154 | ||||||
| chr16:87897164
|
G | A | 4 | a0001c0001t0001g0047a0001c0001t0001g0182a0001c0001t0001g0231others(1): Show | 4 | HG01081.hp1 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+4748C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897164 | ||||||
| chr16:87897173
|
C | T | 8 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.618+4739G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897173 | ||||||
| chr16:87897211
|
C | A | 21 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(18): Show | 21 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.618+4701G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897211 | ||||||
| chr16:87897211
|
C | G | 70 | a0001c0001t0001g0077a0001c0001t0001g0202a0001c0002t0001g0249others(67): Show | 70 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.618+4701G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897211 | ||||||
| chr16:87897238
|
A | G | 12 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(9): Show | 12 | HG02630.hp2 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.618+4674T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897238 | ||||||
| chr16:87897248
|
G | C | 5 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0003g0230others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+4664C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897248 | ||||||
| chr16:87897272
|
G | C | 17 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(14): Show | 17 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.618+4640C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897272 | ||||||
| chr16:87897273
|
A | G | 28 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(25): Show | 28 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.618+4639T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897273 | ||||||
| chr16:87897310
|
A | T | 108 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(105): Show | 108 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.618+4602T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897310 | ||||||
| chr16:87897317
|
G | A | 108 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(105): Show | 108 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.618+4595C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897317 | ||||||
| chr16:87897368
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0071 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.618+4544C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897368 | ||||||
| chr16:87897399
|
C | A | 1 | a0002c0005t0001g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.618+4513G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897399 | ||||||
| chr16:87897448
|
C | T | 7 | a0001c0001t0001g0069a0001c0001t0001g0114a0001c0001t0001g0117others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.618+4464G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897448 | ||||||
| chr16:87897449
|
G | A | 29 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(26): Show | 29 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.618+4463C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897449 | ||||||
| chr16:87897509
|
T | C | 5 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0003g0230others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+4403A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897509 | ||||||
| chr16:87897535
|
C | T | 1 | a0001c0002t0002g0228 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.618+4377G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897535 | ||||||
| chr16:87897536
|
A | G | 105 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(102): Show | 105 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.618+4376T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897536 | ||||||
| chr16:87897675
|
A | G | 123 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(120): Show | 123 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.618+4237T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897675 | ||||||
| chr16:87897875
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | HG00673.hp2 HG02015.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.618+4037C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897875 | ||||||
| chr16:87897897
|
G | A | 80 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(77): Show | 80 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.618+4015C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87897897 | ||||||
| chr16:87898180
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0077a0001c0001t0003g0288 | 3 | HG02451.hp1 HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.618+3732A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898180 | ||||||
| chr16:87898195
|
G | T | 11 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(8): Show | 11 | HG02630.hp2 HG02723.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.618+3717C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898195 | ||||||
| chr16:87898200
|
T | G | 4 | a0001c0001t0001g0060a0001c0001t0001g0359a0002c0005t0001g0022others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+3712A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898200 | ||||||
| chr16:87898374
|
T | C | 20 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(17): Show | 20 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.618+3538A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898374 | ||||||
| chr16:87898518
|
G | C | 2 | a0001c0002t0002g0308a0001c0002t0002g0387 | 2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.618+3394C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898518 | ||||||
| chr16:87898577
|
T | A | 11 | a0001c0001t0001g0048a0001c0001t0001g0189a0001c0001t0001g0190others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.618+3335A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898577 | ||||||
| chr16:87898708
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.618+3204C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898708 | ||||||
| chr16:87898729
|
A | AT | 64 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0043others(61): Show | 64 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.618+3182dupA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898729 | ||||||
| chr16:87898729
|
A | ATT | 10 | a0001c0001t0001g0069a0001c0001t0001g0114a0001c0001t0001g0117others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.618+3181_618+3182d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898729 | ||||||
| chr16:87898729
|
AT | A | 7 | a0001c0001t0001g0059a0001c0001t0001g0077a0001c0001t0001g0361others(4): Show | 7 | HG01192.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.618+3182delA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898729 | ||||||
| chr16:87898750
|
T | C | 1 | a0001c0002t0002g0297 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.618+3162A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898750 | ||||||
| chr16:87898786
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.618+3126C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898786 | ||||||
| chr16:87898830
|
G | A | 4 | a0001c0001t0001g0119a0001c0001t0001g0146a0001c0001t0001g0317others(1): Show | 4 | HG01099.hp2 HG01361.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+3082C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898830 | ||||||
| chr16:87898838
|
GATTCTCC others(561): Show |
G | 3 | a0001c0002t0002g0148a0001c0002t0002g0172a0001c0002t0002g0211 | 3 | HG00438.hp2 NA18955.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.618+2506_618+3073d others(2): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898838 | ||||||
| chr16:87898868
|
G | A | 11 | a0001c0001t0001g0048a0001c0001t0001g0189a0001c0001t0001g0190others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.618+3044C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898868 | ||||||
| chr16:87898872
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.618+3040A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898872 | ||||||
| chr16:87898900
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0077a0001c0001t0003g0288 | 3 | HG02451.hp1 HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.618+3012T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898900 | ||||||
| chr16:87898923
|
C | T | 2 | a0005c0008t0001g0050a0005c0008t0001g0052 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.618+2989G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898923 | ||||||
| chr16:87898991
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.618+2921A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898991 | ||||||
| chr16:87898998
|
G | A | 66 | a0001c0001t0001g0197a0001c0002t0001g0249a0001c0002t0002g0032others(63): Show | 66 | HG00323.hp2 HG00639.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.618+2914C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87898998 | ||||||
| chr16:87899069
|
G | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.618+2843C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899069 | ||||||
| chr16:87899132
|
G | A | 9 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0042others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.618+2780C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899132 | ||||||
| chr16:87899176
|
T | G | 6 | a0001c0001t0001g0142a0001c0001t0001g0168a0001c0001t0001g0194others(3): Show | 6 | HG01261.hp1 HG01361.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.618+2736A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899176 | ||||||
| chr16:87899191
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.618+2721C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899191 | ||||||
| chr16:87899264
|
T | C | 393 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(390): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.618+2648A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899264 | ||||||
| chr16:87899295
|
C | CT | 32 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0078others(29): Show | 32 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.618+2616dupA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899295 | ||||||
| chr16:87899295
|
CT | C | 34 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0080others(31): Show | 34 | HG00609.hp1 HG01069.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.618+2616delA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899295 | ||||||
| chr16:87899295
|
CTT | C | 70 | a0001c0001t0001g0059a0001c0001t0001g0069a0001c0001t0001g0077others(67): Show | 70 | HG00639.hp2 HG00673.hp1 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.618+2615_618+2616d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899295 | ||||||
| chr16:87899295
|
CTTT | C | 28 | a0001c0001t0001g0048a0001c0001t0001g0061a0001c0001t0001g0064others(25): Show | 28 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.618+2614_618+2616d others(5): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899295 | ||||||
| chr16:87899295
|
CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0003g0230others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+2605_618+2616d others(14): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899295 | ||||||
| chr16:87899447
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0077a0001c0001t0003g0288 | 3 | HG02451.hp1 HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.618+2465G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899447 | ||||||
| chr16:87899451
|
C | T | 60 | a0001c0001t0001g0055a0001c0001t0001g0179a0001c0001t0001g0197others(57): Show | 60 | HG00323.hp2 HG00639.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.618+2461G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899451 | ||||||
| chr16:87899456
|
C | T | 1 | a0001c0001t0001g0345 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.618+2456G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899456 | ||||||
| chr16:87899508
|
G | A | 1 | a0001c0002t0002g0216 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.618+2404C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899508 | ||||||
| chr16:87899520
|
T | C | 1 | a0003c0006t0001g0011 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.618+2392A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899520 | ||||||
| chr16:87899537
|
A | G | 1 | a0001c0002t0002g0295 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.618+2375T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899537 | ||||||
| chr16:87899592
|
C | T | 1 | a0001c0001t0001g0328 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.618+2320G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899592 | ||||||
| chr16:87899593
|
G | A | 8 | a0001c0001t0001g0088a0001c0001t0001g0122a0001c0001t0001g0154others(5): Show | 8 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.618+2319C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899593 | ||||||
| chr16:87899594
|
C | T | 1 | a0001c0002t0002g0259 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.618+2318G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899594 | ||||||
| chr16:87899720
|
C | G | 159 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0040others(156): Show | 159 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.618+2192G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899720 | ||||||
| chr16:87899919
|
C | CA | 41 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0035others(38): Show | 41 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.618+1992dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899919
|
C | CAA | 7 | a0001c0001t0001g0205a0001c0001t0001g0246a0001c0001t0001g0278others(4): Show | 7 | HG00438.hp1 HG00741.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.618+1991_618+1992d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899919
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0377 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.618+1979_618+1992d others(16): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899919
|
CA | C | 74 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0044others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.618+1992delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899919
|
CAA | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0051others(22): Show | 26 | HG00609.hp2 HG01081.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.618+1991_618+1992d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899919
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0003g0230others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.618+1985_618+1992d others(10): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899919
|
CAAAAAAA others(2): Show |
C | 23 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0069others(20): Show | 23 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.618+1984_618+1992d others(11): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899919
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0289a0001c0001t0001g0359a0002c0005t0001g0022others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+1983_618+1992d others(12): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899919
|
CAAAAAAA others(4): Show |
C | 11 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(8): Show | 11 | HG02145.hp1 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.618+1982_618+1992d others(13): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899919
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0207 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.618+1981_618+1992d others(14): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899919
|
CAAAAAAA others(7): Show |
C | 4 | a0001c0002t0002g0259a0001c0002t0002g0392a0001c0004t0001g0367others(1): Show | 4 | HG01192.hp2 HG01952.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+1979_618+1992d others(16): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899919
|
CAAAAAAA others(8): Show |
C | 62 | a0001c0001t0001g0179a0001c0002t0001g0249a0001c0002t0002g0032others(59): Show | 62 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.618+1978_618+1992d others(17): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899919
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0351 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.618+1977_618+1992d others(18): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899919
|
CAAAAAAA others(12): Show |
C | 1 | a0003c0006t0001g0004 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.618+1974_618+1992d others(21): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899919 | ||||||
| chr16:87899976
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.618+1936A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87899976 | ||||||
| chr16:87900009
|
C | A | 7 | a0001c0002t0002g0087a0001c0003t0002g0041a0001c0003t0002g0054others(4): Show | 7 | HG01891.hp2 HG02622.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.618+1903G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87900009 | ||||||
| chr16:87900022
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0325 | 2 | HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.618+1890C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87900022 | ||||||
| chr16:87900039
|
C | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0268 | 2 | NA18942.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.618+1873G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87900039 | ||||||
| chr16:87900063
|
C | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0277 | 2 | NA19082.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.618+1849G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87900063 | ||||||
| chr16:87900143
|
T | C | 4 | a0001c0003t0002g0075a0001c0003t0002g0090a0001c0003t0002g0185others(1): Show | 4 | HG01070.hp1 HG01168.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+1769A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87900143 | ||||||
| chr16:87900164
|
T | C | 124 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(121): Show | 124 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.618+1748A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87900164 | ||||||
| chr16:87900227
|
G | A | 8 | a0001c0002t0002g0033a0001c0002t0002g0073a0001c0002t0002g0074others(5): Show | 8 | HG00323.hp2 HG01257.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.618+1685C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87900227 | ||||||
| chr16:87900242
|
C | G | 1 | a0001c0002t0002g0087 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.618+1670G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87900242 | ||||||
| chr16:87900378
|
A | G | 25 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0047others(22): Show | 25 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.618+1534T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87900378 | ||||||
| chr16:87900408
|
C | T | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+1504G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87900408 | ||||||
| chr16:87900516
|
T | C | 1 | a0001c0001t0001g0396 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.618+1396A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87900516 | ||||||
| chr16:87900528
|
G | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+1384C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87900528 | ||||||
| chr16:87900562
|
C | A | 6 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0073others(3): Show | 6 | HG01257.hp1 HG01515.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.618+1350G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87900562 | ||||||
| chr16:87901162
|
G | A | 3 | a0001c0001t0001g0047a0001c0001t0001g0231a0001c0001t0001g0291 | 3 | HG01081.hp1 HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.618+750C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87901162 | ||||||
| chr16:87901176
|
G | A | 5 | a0001c0002t0002g0232a0001c0002t0002g0285a0001c0002t0002g0286others(2): Show | 5 | HG00639.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+736C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87901176 | ||||||
| chr16:87901409
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.618+503C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87901409 | ||||||
| chr16:87901409
|
G | T | 4 | a0001c0003t0002g0041a0001c0003t0002g0054a0001c0003t0002g0379others(1): Show | 4 | HG01891.hp2 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+503C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87901409 | ||||||
| chr16:87901475
|
G | A | 1 | a0001c0002t0002g0247 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.618+437C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87901475 | ||||||
| chr16:87901578
|
C | CTTTCT | 88 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(85): Show | 88 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.618+329_618+333dup others(5): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87901578 | ||||||
| chr16:87901592
|
C | CTTTTCT | 14 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0069others(11): Show | 14 | HG01175.hp2 HG02630.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.618+319_618+320ins others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87901592 | ||||||
| chr16:87901778
|
G | C | 10 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0003g0230others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.618+134C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87901778 | ||||||
| chr16:87901807
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.618+105C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87901807 | ||||||
| chr16:87901868
|
T | C | 2 | a0001c0001t0001g0356a0001c0001t0001g0397 | 2 | HG01192.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.618+44A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | 87901868 | ||||||
| chr16:87902003
|
T | C | 1 | a0001c0003t0002g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.556-29A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 4/6 | chr16 | 87902003 | ||||||
| chr16:87902022
|
G | A | 4 | a0001c0001t0001g0093a0001c0001t0001g0140a0001c0001t0001g0256others(1): Show | 4 | HG00609.hp1 NA18612.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-48C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 4/6 | chr16 | 87902022 | ||||||
| chr16:87902022
|
G | C | 39 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(36): Show | 39 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.556-48C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 4/6 | chr16 | 87902022 | ||||||
| chr16:87902026
|
G | A | 2 | a0001c0013t0001g0321a0001c0014t0001g0102 | 2 | HG01433.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.556-52C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 4/6 | chr16 | 87902026 | ||||||
| chr16:87902290
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.555+135C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 4/6 | chr16 | 87902290 | ||||||
| chr16:87902308
|
T | G | 3 | a0001c0001t0001g0359a0002c0005t0001g0022a0003c0006t0001g0009 | 3 | HG01109.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.555+117A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 4/6 | chr16 | 87902308 | ||||||
| chr16:87902352
|
C | CA | 75 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(72): Show | 75 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.555+72dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 4/6 | chr16 | 87902352 | ||||||
| chr16:87902352
|
CA | C | 7 | a0001c0001t0001g0069a0001c0001t0001g0114a0001c0001t0001g0117others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+72delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 4/6 | chr16 | 87902352 | ||||||
| chr16:87902393
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.555+32A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 4/6 | chr16 | 87902393 | ||||||
| chr16:87902554
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-34G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902554 | ||||||
| chr16:87902555
|
A | G | 39 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(36): Show | 39 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.460-35T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902555 | ||||||
| chr16:87902581
|
C | A | 10 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0003g0230others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-61G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902581 | ||||||
| chr16:87902661
|
C | T | 11 | a0001c0001t0001g0048a0001c0001t0001g0189a0001c0001t0001g0190others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.460-141G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902661 | ||||||
| chr16:87902750
|
CA | C | 114 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(111): Show | 114 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.460-231delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902750 | ||||||
| chr16:87902773
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0003g0288 | 2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.460-253C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902773 | ||||||
| chr16:87902817
|
C | A | 1 | a0001c0001t0001g0322 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.460-297G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902817 | ||||||
| chr16:87902895
|
G | C | 3 | a0001c0001t0001g0182a0005c0008t0001g0050a0005c0008t0001g0052 | 3 | HG03041.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.460-375C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902895 | ||||||
| chr16:87902907
|
A | G | 10 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0003g0230others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-387T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902907 | ||||||
| chr16:87902908
|
T | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0325 | 2 | HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.460-388A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902908 | ||||||
| chr16:87902913
|
CA | C | 44 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(41): Show | 44 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.460-394delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902913 | ||||||
| chr16:87902940
|
T | G | 1 | a0001c0001t0003g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.460-420A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902940 | ||||||
| chr16:87902982
|
G | C | 1 | a0001c0001t0001g0344 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.460-462C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902982 | ||||||
| chr16:87902992
|
G | A | 12 | a0001c0001t0001g0025a0001c0001t0001g0097a0001c0001t0001g0098others(9): Show | 12 | HG00621.hp2 HG01981.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.460-472C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87902992 | ||||||
| chr16:87903037
|
G | GC | 7 | a0001c0001t0001g0069a0001c0001t0001g0114a0001c0001t0001g0117others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.460-518_460-517ins others(1): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903037 | ||||||
| chr16:87903037
|
G | T | 1 | a0001c0004t0001g0367 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.460-517C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903037 | ||||||
| chr16:87903039
|
G | A | 1 | a0001c0003t0002g0219 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.460-519C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903039 | ||||||
| chr16:87903039
|
G | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0347a0001c0002t0002g0172 | 3 | NA18955.hp2 NA18961.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.460-519C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903039 | ||||||
| chr16:87903150
|
C | T | 2 | a0001c0001t0001g0063a0001c0012t0001g0388 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.460-630G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903150 | ||||||
| chr16:87903347
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0058others(1): Show | 4 | NA18943.hp1 NA18975.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-827G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903347 | ||||||
| chr16:87903378
|
C | T | 24 | a0001c0001t0001g0048a0001c0001t0001g0182a0001c0001t0001g0189others(21): Show | 24 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.460-858G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903378 | ||||||
| chr16:87903386
|
G | A | 1 | a0001c0003t0002g0183 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.460-866C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903386 | ||||||
| chr16:87903387
|
T | C | 42 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(39): Show | 42 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.460-867A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903387 | ||||||
| chr16:87903467
|
T | G | 1 | a0002c0005t0001g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.460-947A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903467 | ||||||
| chr16:87903549
|
ATTG | A | 59 | a0001c0002t0001g0249a0001c0002t0002g0032a0001c0002t0002g0033others(56): Show | 59 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.460-1032_460-1030d others(5): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903549 | ||||||
| chr16:87903576
|
T | C | 4 | a0001c0003t0002g0041a0001c0003t0002g0054a0001c0003t0002g0379others(1): Show | 4 | HG01891.hp2 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1056A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903576 | ||||||
| chr16:87903781
|
T | G | 5 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0003g0230others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+1005A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903781 | ||||||
| chr16:87903958
|
A | C | 7 | a0001c0001t0001g0070a0001c0001t0001g0119a0001c0001t0001g0146others(4): Show | 7 | HG01099.hp2 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.459+828T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903958 | ||||||
| chr16:87903967
|
A | G | 11 | a0001c0001t0001g0048a0001c0001t0001g0189a0001c0001t0001g0190others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.459+819T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87903967 | ||||||
| chr16:87904043
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.459+743A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904043 | ||||||
| chr16:87904056
|
T | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0176 | 2 | NA18986.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.459+730A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904056 | ||||||
| chr16:87904060
|
A | G | 55 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(52): Show | 55 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.459+726T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904060 | ||||||
| chr16:87904073
|
G | A | 1 | a0001c0003t0002g0383 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.459+713C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904073 | ||||||
| chr16:87904079
|
C | T | 57 | a0001c0002t0001g0249a0001c0002t0002g0032a0001c0002t0002g0033others(54): Show | 57 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.459+707G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904079 | ||||||
| chr16:87904140
|
G | C | 1 | a0001c0004t0001g0279 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.459+646C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904140 | ||||||
| chr16:87904234
|
C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0318 | 2 | HG03017.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.459+552G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904234 | ||||||
| chr16:87904320
|
T | A | 1 | a0002c0005t0001g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.459+466A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904320 | ||||||
| chr16:87904333
|
C | G | 58 | a0001c0002t0001g0249a0001c0002t0002g0032a0001c0002t0002g0033others(55): Show | 58 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.459+453G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904333 | ||||||
| chr16:87904340
|
C | CA | 19 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(16): Show | 19 | HG01099.hp2 HG01515.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.459+445dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904340 | ||||||
| chr16:87904340
|
C | CAA | 45 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(42): Show | 45 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.459+444_459+445dup others(2): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904340 | ||||||
| chr16:87904364
|
AAAAC | A | 11 | a0001c0001t0001g0048a0001c0001t0001g0189a0001c0001t0001g0190others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.459+418_459+421del others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904364 | ||||||
| chr16:87904627
|
C | G | 1 | a0001c0001t0001g0208 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.459+159G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904627 | ||||||
| chr16:87904702
|
C | T | 8 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0073others(5): Show | 8 | HG00323.hp2 HG01257.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+84G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904702 | ||||||
| chr16:87904735
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.459+51G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904735 | ||||||
| chr16:87904761
|
G | A | 1 | a0006c0015t0001g0398 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.459+25C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 3/6 | chr16 | 87904761 | ||||||
| chr16:87904995
|
T | C | 1 | a0001c0003t0002g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.341-91A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87904995 | ||||||
| chr16:87905039
|
C | A | 1 | a0001c0001t0001g0106 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.341-135G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905039 | ||||||
| chr16:87905089
|
C | G | 22 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0142others(19): Show | 22 | HG01261.hp1 HG01361.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.341-185G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905089 | ||||||
| chr16:87905093
|
C | A | 56 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0039others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.341-189G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905093 | ||||||
| chr16:87905093
|
C | G | 1 | a0001c0001t0001g0240 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.341-189G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905093 | ||||||
| chr16:87905093
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.341-189G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905093 | ||||||
| chr16:87905094
|
C | G | 123 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(120): Show | 123 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.341-190G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905094 | ||||||
| chr16:87905104
|
C | T | 18 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.341-200G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905104 | ||||||
| chr16:87905177
|
G | A | 61 | a0001c0002t0001g0249a0001c0002t0002g0032a0001c0002t0002g0033others(58): Show | 61 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.341-273C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905177 | ||||||
| chr16:87905251
|
C | T | 46 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(43): Show | 46 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.341-347G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905251 | ||||||
| chr16:87905258
|
TA | T | 12 | a0001c0001t0001g0048a0001c0001t0001g0189a0001c0001t0001g0190others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.341-355delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905258 | ||||||
| chr16:87905272
|
T | A | 3 | a0001c0001t0001g0359a0002c0005t0001g0022a0003c0006t0001g0009 | 3 | HG01109.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.341-368A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905272 | ||||||
| chr16:87905408
|
G | A | 35 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0036others(32): Show | 35 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.341-504C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905408 | ||||||
| chr16:87905505
|
T | C | 58 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(55): Show | 58 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.341-601A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905505 | ||||||
| chr16:87905557
|
C | G | 46 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(43): Show | 46 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.341-653G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905557 | ||||||
| chr16:87905560
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.341-656A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905560 | ||||||
| chr16:87905564
|
A | G | 46 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(43): Show | 46 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.341-660T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905564 | ||||||
| chr16:87905568
|
A | G | 46 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(43): Show | 46 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.341-664T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905568 | ||||||
| chr16:87905589
|
T | C | 46 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(43): Show | 46 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.341-685A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905589 | ||||||
| chr16:87905623
|
C | T | 43 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(40): Show | 43 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.341-719G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905623 | ||||||
| chr16:87905649
|
G | A | 1 | a0001c0003t0002g0379 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.341-745C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905649 | ||||||
| chr16:87905683
|
C | T | 1 | a0001c0001t0001g0376 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.341-779G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905683 | ||||||
| chr16:87905718
|
T | A | 2 | a0001c0004t0001g0131a0001c0004t0001g0337 | 2 | NA19070.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.341-814A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905718 | ||||||
| chr16:87905764
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.341-860T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905764 | ||||||
| chr16:87905817
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0116 | 2 | HG00639.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.341-913T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905817 | ||||||
| chr16:87905837
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.341-933G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905837 | ||||||
| chr16:87905864
|
A | G | 123 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(120): Show | 123 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.341-960T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905864 | ||||||
| chr16:87905916
|
G | A | 11 | a0001c0001t0001g0048a0001c0001t0001g0189a0001c0001t0001g0190others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.341-1012C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905916 | ||||||
| chr16:87905937
|
T | C | 118 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(115): Show | 118 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.341-1033A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87905937 | ||||||
| chr16:87906039
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.341-1135C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906039 | ||||||
| chr16:87906046
|
T | C | 28 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0001g0077others(25): Show | 28 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.341-1142A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906046 | ||||||
| chr16:87906096
|
C | A | 5 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0003g0230others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-1192G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906096 | ||||||
| chr16:87906129
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.341-1225C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906129 | ||||||
| chr16:87906231
|
C | CCTCGTGT others(11): Show |
119 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(116): Show | 119 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.341-1328_341-1327i others(20): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906231 | ||||||
| chr16:87906231
|
C | CCTCGTTT others(11): Show |
3 | a0001c0001t0001g0059a0001c0001t0001g0077a0001c0001t0003g0288 | 3 | HG02451.hp1 HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.341-1328_341-1327i others(20): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906231 | ||||||
| chr16:87906329
|
G | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-1425C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906329 | ||||||
| chr16:87906491
|
G | C | 15 | a0001c0001t0001g0048a0001c0001t0001g0182a0001c0001t0001g0189others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.341-1587C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906491 | ||||||
| chr16:87906536
|
A | G | 77 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(74): Show | 77 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.341-1632T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906536 | ||||||
| chr16:87906578
|
G | C | 1 | a0001c0001t0001g0246 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.341-1674C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906578 | ||||||
| chr16:87906603
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.341-1699C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906603 | ||||||
| chr16:87906877
|
T | G | 1 | a0001c0002t0002g0087 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.341-1973A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906877 | ||||||
| chr16:87906883
|
A | G | 5 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-1979T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906883 | ||||||
| chr16:87906948
|
G | A | 1 | a0003c0006t0001g0011 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.341-2044C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906948 | ||||||
| chr16:87906955
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.341-2051C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87906955 | ||||||
| chr16:87907039
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.341-2135T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87907039 | ||||||
| chr16:87907175
|
G | A | 10 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(7): Show | 10 | HG02630.hp2 HG02723.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.341-2271C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87907175 | ||||||
| chr16:87907190
|
C | T | 3 | a0001c0001t0001g0359a0002c0005t0001g0022a0003c0006t0001g0009 | 3 | HG01109.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.341-2286G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87907190 | ||||||
| chr16:87907217
|
CA | C | 11 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(8): Show | 11 | HG02630.hp2 HG02723.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.341-2314delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87907217 | ||||||
| chr16:87907251
|
G | C | 2 | a0001c0001t0001g0096a0003c0006t0001g0011 | 2 | HG02145.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.341-2347C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87907251 | ||||||
| chr16:87907286
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.341-2382G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87907286 | ||||||
| chr16:87907414
|
C | A | 9 | a0001c0001t0001g0047a0001c0001t0001g0069a0001c0001t0001g0114others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.341-2510G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87907414 | ||||||
| chr16:87907417
|
C | G | 24 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0064others(21): Show | 24 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.341-2513G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87907417 | ||||||
| chr16:87907420
|
A | AG | 11 | a0001c0001t0001g0048a0001c0001t0001g0189a0001c0001t0001g0190others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.341-2517dupC | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87907420 | ||||||
| chr16:87907574
|
G | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-2670C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87907574 | ||||||
| chr16:87907953
|
G | A | 39 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0061others(36): Show | 39 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.341-3049C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87907953 | ||||||
| chr16:87907957
|
T | C | 39 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0061others(36): Show | 39 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.341-3053A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87907957 | ||||||
| chr16:87907995
|
A | T | 12 | a0001c0001t0001g0048a0001c0001t0001g0189a0001c0001t0001g0190others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.341-3091T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87907995 | ||||||
| chr16:87908057
|
C | T | 2 | a0001c0001t0001g0038a0001c0002t0002g0228 | 2 | HG02451.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.341-3153G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908057 | ||||||
| chr16:87908084
|
TATTC | T | 9 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.341-3184_341-3181d others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908084 | ||||||
| chr16:87908163
|
C | T | 12 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(9): Show | 12 | HG02630.hp2 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.341-3259G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908163 | ||||||
| chr16:87908164
|
G | A | 1 | a0001c0002t0002g0177 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.341-3260C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908164 | ||||||
| chr16:87908175
|
C | G | 2 | a0001c0002t0002g0087a0001c0012t0001g0388 | 2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.341-3271G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908175 | ||||||
| chr16:87908385
|
T | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0071 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.341-3481A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908385 | ||||||
| chr16:87908389
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.341-3485C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908389 | ||||||
| chr16:87908391
|
A | G | 1 | a0001c0001t0001g0320 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.341-3487T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908391 | ||||||
| chr16:87908397
|
C | T | 1 | a0001c0002t0002g0331 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.341-3493G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908397 | ||||||
| chr16:87908398
|
A | C | 1 | a0001c0002t0002g0331 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.341-3494T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908398 | ||||||
| chr16:87908400
|
C | G | 1 | a0001c0002t0002g0331 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.341-3496G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908400 | ||||||
| chr16:87908403
|
T | A | 1 | a0001c0002t0002g0331 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.341-3499A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908403 | ||||||
| chr16:87908413
|
C | T | 2 | a0001c0003t0002g0248a0001c0003t0002g0355 | 2 | HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.341-3509G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908413 | ||||||
| chr16:87908466
|
C | A | 1 | a0001c0001t0001g0376 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.341-3562G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908466 | ||||||
| chr16:87908547
|
G | A | 1 | a0001c0002t0002g0087 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.341-3643C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908547 | ||||||
| chr16:87908594
|
G | C | 77 | a0001c0001t0001g0043a0001c0001t0001g0077a0001c0001t0001g0199others(74): Show | 77 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.341-3690C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908594 | ||||||
| chr16:87908662
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.341-3758C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908662 | ||||||
| chr16:87908751
|
C | A | 16 | a0001c0001t0001g0048a0001c0001t0001g0066a0001c0001t0001g0189others(13): Show | 16 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.341-3847G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908751 | ||||||
| chr16:87908818
|
G | T | 119 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0045others(116): Show | 119 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.341-3914C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908818 | ||||||
| chr16:87908825
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.341-3921G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908825 | ||||||
| chr16:87908850
|
CT | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0231a0001c0001t0001g0291 | 3 | HG01081.hp1 HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.341-3947delA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908850 | ||||||
| chr16:87908914
|
C | T | 1 | a0001c0001t0003g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.341-4010G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908914 | ||||||
| chr16:87908973
|
A | G | 2 | a0001c0001t0001g0200a0003c0006t0001g0004 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.341-4069T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908973 | ||||||
| chr16:87908989
|
A | AT | 32 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0088others(29): Show | 32 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.341-4086dupA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908989 | ||||||
| chr16:87908989
|
A | ATTTT | 15 | a0001c0001t0001g0048a0001c0001t0001g0066a0001c0001t0001g0189others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.341-4089_341-4086d others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908989 | ||||||
| chr16:87908989
|
A | ATTTTT | 12 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0072others(9): Show | 12 | HG02486.hp2 HG02630.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.341-4090_341-4086d others(7): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908989 | ||||||
| chr16:87908989
|
AT | A | 98 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0063others(95): Show | 98 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.341-4086delA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87908989 | ||||||
| chr16:87909042
|
A | G | 6 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0073others(3): Show | 6 | HG01257.hp1 HG01515.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-4138T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909042 | ||||||
| chr16:87909124
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.341-4220G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909124 | ||||||
| chr16:87909132
|
C | G | 29 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0066others(26): Show | 29 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.341-4228G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909132 | ||||||
| chr16:87909176
|
C | G | 1 | a0001c0013t0001g0321 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.341-4272G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909176 | ||||||
| chr16:87909205
|
C | T | 5 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-4301G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909205 | ||||||
| chr16:87909206
|
A | G | 5 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(2): Show | 5 | NA18978.hp1 NA18983.hp1 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-4302T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909206 | ||||||
| chr16:87909263
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.341-4359C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909263 | ||||||
| chr16:87909365
|
G | A | 22 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0048others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.341-4461C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909365 | ||||||
| chr16:87909403
|
A | G | 12 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0096others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.341-4499T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909403 | ||||||
| chr16:87909433
|
G | C | 1 | a0001c0001t0001g0275 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.341-4529C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909433 | ||||||
| chr16:87909471
|
G | A | 20 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0061others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.341-4567C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909471 | ||||||
| chr16:87909537
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.341-4633G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909537 | ||||||
| chr16:87909553
|
G | C | 1 | a0001c0002t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.341-4649C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909553 | ||||||
| chr16:87909558
|
A | G | 1 | a0001c0001t0001g0378 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.341-4654T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909558 | ||||||
| chr16:87909568
|
A | G | 397 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(394): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.341-4664T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909568 | ||||||
| chr16:87909631
|
G | A | 4 | a0001c0001t0001g0100a0001c0001t0001g0188a0001c0001t0001g0201others(1): Show | 4 | HG00738.hp2 HG01952.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-4727C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909631 | ||||||
| chr16:87909635
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0256a0001c0001t0001g0273 | 3 | HG00609.hp1 NA18979.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.341-4731A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909635 | ||||||
| chr16:87909674
|
G | A | 1 | a0001c0004t0001g0323 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.341-4770C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909674 | ||||||
| chr16:87909689
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(213): Show | 218 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.341-4785C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909689 | ||||||
| chr16:87909798
|
C | T | 14 | a0001c0001t0001g0026a0001c0001t0001g0121a0001c0001t0001g0196others(11): Show | 14 | HG00438.hp1 HG01081.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.341-4894G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909798 | ||||||
| chr16:87909851
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.341-4947G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909851 | ||||||
| chr16:87909863
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.341-4959A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909863 | ||||||
| chr16:87909988
|
G | A | 1 | a0001c0002t0002g0391 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.341-5084C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87909988 | ||||||
| chr16:87910007
|
T | C | 11 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0289others(8): Show | 11 | HG01891.hp2 HG02615.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.341-5103A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910007 | ||||||
| chr16:87910069
|
T | G | 10 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0068others(7): Show | 10 | HG01167.hp1 HG02280.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.341-5165A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910069 | ||||||
| chr16:87910084
|
AAAAC | A | 79 | a0001c0001t0001g0039a0001c0001t0001g0051a0001c0001t0001g0070others(76): Show | 79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.341-5184_341-5181d others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910084 | ||||||
| chr16:87910139
|
G | A | 7 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0042others(4): Show | 7 | HG02055.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.341-5235C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910139 | ||||||
| chr16:87910181
|
G | A | 137 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0038others(134): Show | 137 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(134): Show |
intron_variant | MODIFIER | c.341-5277C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910181 | ||||||
| chr16:87910256
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.341-5352C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910256 | ||||||
| chr16:87910257
|
T | C | 1 | a0001c0002t0002g0241 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.341-5353A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910257 | ||||||
| chr16:87910271
|
G | A | 2 | a0001c0001t0001g0208a0001c0003t0002g0355 | 2 | HG03491.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.341-5367C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910271 | ||||||
| chr16:87910287
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.341-5383C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910287 | ||||||
| chr16:87910317
|
G | A | 10 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0042others(7): Show | 10 | HG02055.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.341-5413C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910317 | ||||||
| chr16:87910365
|
C | T | 84 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0039others(81): Show | 84 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.341-5461G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910365 | ||||||
| chr16:87910411
|
G | A | 1 | a0001c0001t0001g0393 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.341-5507C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910411 | ||||||
| chr16:87910433
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0123others(1): Show | 4 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-5529G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910433 | ||||||
| chr16:87910436
|
A | T | 3 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301 | 3 | NA18978.hp1 NA18983.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.341-5532T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910436 | ||||||
| chr16:87910498
|
C | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0084a0001c0001t0001g0171others(2): Show | 5 | HG02155.hp1 NA18949.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-5594G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910498 | ||||||
| chr16:87910509
|
C | G | 75 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0039others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.341-5605G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910509 | ||||||
| chr16:87910555
|
C | T | 5 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0066others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-5651G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910555 | ||||||
| chr16:87910562
|
G | A | 1 | a0001c0004t0001g0279 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.341-5658C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910562 | ||||||
| chr16:87910612
|
C | T | 11 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0042others(8): Show | 11 | HG02055.hp1 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.341-5708G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910612 | ||||||
| chr16:87910614
|
G | C | 1 | a0002c0005t0001g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.341-5710C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910614 | ||||||
| chr16:87910632
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG01070.hp2 HG01071.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.341-5728G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910632 | ||||||
| chr16:87910633
|
G | C | 1 | a0002c0005t0001g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.341-5729C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910633 | ||||||
| chr16:87910653
|
C | T | 72 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0046others(69): Show | 72 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.341-5749G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910653 | ||||||
| chr16:87910720
|
G | A | 5 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0066others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-5816C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910720 | ||||||
| chr16:87910744
|
ATTTTTG | A | 9 | a0001c0001t0001g0061a0001c0001t0001g0289a0001c0001t0001g0290others(6): Show | 9 | HG02258.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-5846_341-5841d others(8): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910744 | ||||||
| chr16:87910782
|
T | G | 2 | a0001c0001t0001g0207a0001c0004t0001g0274 | 2 | NA18967.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.341-5878A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910782 | ||||||
| chr16:87910810
|
C | T | 9 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0233others(6): Show | 9 | HG00639.hp2 HG01243.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-5906G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910810 | ||||||
| chr16:87910818
|
T | C | 48 | a0001c0001t0001g0031a0001c0001t0001g0085a0001c0001t0001g0110others(45): Show | 48 | HG00099.hp2 HG00544.hp2 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.341-5914A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910818 | ||||||
| chr16:87910843
|
G | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0175 | 2 | HG03834.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.341-5939C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910843 | ||||||
| chr16:87910859
|
C | T | 2 | a0001c0001t0001g0159a0001c0003t0002g0156 | 2 | HG00544.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.341-5955G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910859 | ||||||
| chr16:87910940
|
G | A | 128 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0037others(125): Show | 128 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.341-6036C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87910940 | ||||||
| chr16:87911099
|
C | CA | 7 | a0001c0001t0001g0069a0001c0001t0001g0143a0001c0001t0001g0144others(4): Show | 7 | HG01175.hp2 NA18963.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.341-6196dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911099 | ||||||
| chr16:87911099
|
C | CAA | 11 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0040others(8): Show | 11 | HG02074.hp2 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.341-6197_341-6196d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911099 | ||||||
| chr16:87911099
|
CA | C | 80 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0057others(77): Show | 80 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.341-6196delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911099 | ||||||
| chr16:87911099
|
CAA | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0089others(4): Show | 7 | HG01516.hp2 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.341-6197_341-6196d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911099 | ||||||
| chr16:87911099
|
CAAAAAAA | C | 80 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0039others(77): Show | 80 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.341-6202_341-6196d others(9): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911099 | ||||||
| chr16:87911117
|
A | T | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.341-6213T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911117 | ||||||
| chr16:87911137
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.341-6233C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911137 | ||||||
| chr16:87911202
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.341-6298G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911202 | ||||||
| chr16:87911259
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.341-6355C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911259 | ||||||
| chr16:87911259
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.341-6355C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911259 | ||||||
| chr16:87911273
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.341-6369A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911273 | ||||||
| chr16:87911287
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.341-6383G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911287 | ||||||
| chr16:87911303
|
A | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0291a0001c0001t0001g0366others(1): Show | 4 | HG01081.hp1 HG01358.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-6399T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911303 | ||||||
| chr16:87911328
|
C | T | 5 | a0001c0001t0001g0063a0001c0001t0001g0182a0001c0001t0001g0360others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-6424G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911328 | ||||||
| chr16:87911380
|
C | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0089a0001c0012t0001g0388 | 3 | HG02145.hp2 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.341-6476G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911380 | ||||||
| chr16:87911446
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.341-6542T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911446 | ||||||
| chr16:87911564
|
G | A | 1 | a0001c0002t0002g0324 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.341-6660C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911564 | ||||||
| chr16:87911569
|
C | T | 5 | a0001c0001t0001g0063a0001c0001t0001g0182a0001c0001t0001g0360others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-6665G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911569 | ||||||
| chr16:87911609
|
GAC | G | 67 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0046others(64): Show | 67 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.341-6707_341-6706d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911609 | ||||||
| chr16:87911623
|
C | G | 9 | a0001c0001t0001g0061a0001c0001t0001g0289a0001c0001t0001g0290others(6): Show | 9 | HG02258.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-6719G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911623 | ||||||
| chr16:87911666
|
T | C | 59 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0094others(56): Show | 59 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.341-6762A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911666 | ||||||
| chr16:87911685
|
A | T | 10 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0077others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.341-6781T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911685 | ||||||
| chr16:87911692
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.341-6788G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911692 | ||||||
| chr16:87911748
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.341-6844C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911748 | ||||||
| chr16:87911850
|
A | G | 74 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0046others(71): Show | 74 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.341-6946T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911850 | ||||||
| chr16:87911955
|
A | G | 6 | a0001c0001t0001g0068a0001c0001t0001g0154a0001c0001t0001g0365others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-7051T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87911955 | ||||||
| chr16:87912054
|
C | T | 65 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0046others(62): Show | 65 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.341-7150G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912054 | ||||||
| chr16:87912086
|
G | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0382a0002c0005t0001g0024 | 3 | HG02055.hp2 HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.341-7182C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912086 | ||||||
| chr16:87912208
|
G | C | 3 | a0001c0001t0001g0377a0001c0003t0002g0383a0003c0006t0001g0003 | 3 | HG02647.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.341-7304C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912208 | ||||||
| chr16:87912235
|
C | G | 191 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0037others(188): Show | 191 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.341-7331G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912235 | ||||||
| chr16:87912257
|
G | A | 65 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0046others(62): Show | 65 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.341-7353C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912257 | ||||||
| chr16:87912369
|
C | T | 2 | a0001c0002t0002g0213a0001c0002t0002g0282 | 2 | HG02155.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.341-7465G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912369 | ||||||
| chr16:87912394
|
G | A | 15 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0077others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.341-7490C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912394 | ||||||
| chr16:87912417
|
G | A | 5 | a0001c0001t0001g0063a0001c0001t0001g0182a0001c0001t0001g0360others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-7513C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912417 | ||||||
| chr16:87912427
|
C | T | 1 | a0001c0004t0001g0151 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.341-7523G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912427 | ||||||
| chr16:87912505
|
G | C | 10 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0042others(7): Show | 10 | HG02055.hp1 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.341-7601C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912505 | ||||||
| chr16:87912521
|
T | C | 9 | a0001c0001t0001g0061a0001c0001t0001g0289a0001c0001t0001g0290others(6): Show | 9 | HG02258.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-7617A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912521 | ||||||
| chr16:87912527
|
C | T | 14 | a0001c0001t0001g0046a0001c0001t0001g0062a0001c0001t0001g0066others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.341-7623G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912527 | ||||||
| chr16:87912540
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.341-7636A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912540 | ||||||
| chr16:87912543
|
C | G | 104 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(101): Show | 104 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.341-7639G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912543 | ||||||
| chr16:87912552
|
A | G | 113 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(110): Show | 113 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.341-7648T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912552 | ||||||
| chr16:87912647
|
G | A | 60 | a0001c0001t0001g0038a0001c0001t0001g0078a0001c0001t0001g0080others(57): Show | 60 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.341-7743C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912647 | ||||||
| chr16:87912686
|
G | C | 10 | a0001c0001t0001g0062a0001c0001t0001g0077a0001c0001t0001g0231others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.341-7782C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912686 | ||||||
| chr16:87912699
|
G | A | 9 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0048others(6): Show | 9 | HG02055.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.341-7795C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912699 | ||||||
| chr16:87912705
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.341-7801T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912705 | ||||||
| chr16:87912713
|
T | G | 1 | a0001c0001t0001g0374 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.341-7809A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912713 | ||||||
| chr16:87912722
|
C | T | 1 | a0002c0005t0001g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.341-7818G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912722 | ||||||
| chr16:87912776
|
T | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.341-7872A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912776 | ||||||
| chr16:87912777
|
A | G | 1 | a0001c0002t0002g0087 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.341-7873T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912777 | ||||||
| chr16:87912827
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0068 | 2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.341-7923C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912827 | ||||||
| chr16:87912859
|
C | T | 9 | a0001c0001t0001g0062a0001c0001t0001g0077a0001c0001t0001g0231others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.341-7955G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912859 | ||||||
| chr16:87912882
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.341-7978C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912882 | ||||||
| chr16:87912885
|
G | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0198a0001c0001t0001g0284others(2): Show | 5 | HG01167.hp1 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-7981C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912885 | ||||||
| chr16:87912989
|
G | GT | 65 | a0001c0001t0001g0038a0001c0001t0001g0069a0001c0001t0001g0078others(62): Show | 65 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.341-8086dupA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87912989 | ||||||
| chr16:87913075
|
C | T | 6 | a0001c0001t0001g0062a0001c0001t0001g0077a0001c0001t0001g0231others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-8171G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913075 | ||||||
| chr16:87913077
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.341-8173T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913077 | ||||||
| chr16:87913117
|
T | A | 161 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(158): Show | 161 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.341-8213A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913117 | ||||||
| chr16:87913197
|
T | G | 163 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(160): Show | 163 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.341-8293A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913197 | ||||||
| chr16:87913223
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.341-8319G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913223 | ||||||
| chr16:87913249
|
G | A | 186 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0037others(183): Show | 186 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.341-8345C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913249 | ||||||
| chr16:87913259
|
G | A | 11 | a0001c0001t0001g0046a0001c0001t0001g0063a0001c0001t0001g0066others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.341-8355C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913259 | ||||||
| chr16:87913261
|
G | A | 9 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0042others(6): Show | 9 | HG02055.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-8357C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913261 | ||||||
| chr16:87913305
|
C | CTTTTT | 65 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0047others(62): Show | 65 | HG00099.hp2 HG00544.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.341-8406_341-8402d others(7): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913305 | ||||||
| chr16:87913305
|
C | CTTTTTTT others(2): Show |
33 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(30): Show | 33 | HG00639.hp2 HG01167.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.341-8410_341-8402d others(11): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913305 | ||||||
| chr16:87913305
|
C | CTTTTTTT others(3): Show |
1 | a0001c0003t0002g0379 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.341-8411_341-8402d others(12): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913305 | ||||||
| chr16:87913305
|
CT | C | 71 | a0001c0001t0001g0038a0001c0001t0001g0078a0001c0001t0001g0080others(68): Show | 71 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.341-8402delA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913305 | ||||||
| chr16:87913328
|
G | A | 77 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0047others(74): Show | 77 | HG00099.hp2 HG00544.hp2 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.341-8424C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913328 | ||||||
| chr16:87913342
|
A | G | 11 | a0001c0001t0001g0061a0001c0001t0001g0199a0001c0001t0001g0200others(8): Show | 11 | HG02258.hp1 HG02615.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.341-8438T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913342 | ||||||
| chr16:87913373
|
C | G | 395 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(392): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.341-8469G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913373 | ||||||
| chr16:87913384
|
C | T | 1 | a0001c0003t0002g0383 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.341-8480G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913384 | ||||||
| chr16:87913400
|
G | A | 74 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(71): Show | 74 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.341-8496C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913400 | ||||||
| chr16:87913463
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.341-8559A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913463 | ||||||
| chr16:87913579
|
C | T | 4 | a0001c0001t0001g0176a0001c0004t0001g0133a0001c0004t0001g0338others(1): Show | 4 | HG02132.hp1 NA18964.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-8675G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913579 | ||||||
| chr16:87913659
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.341-8755G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913659 | ||||||
| chr16:87913660
|
CCTCCT | C | 14 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.341-8761_341-8757d others(7): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913660 | ||||||
| chr16:87913661
|
CT | C | 68 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(65): Show | 68 | HG00280.hp2 HG00639.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.341-8758delA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913661 | ||||||
| chr16:87913662
|
T | C | 25 | a0001c0001t0001g0057a0001c0001t0001g0097a0001c0001t0001g0130others(22): Show | 25 | HG00438.hp2 HG00544.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.341-8758A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913662 | ||||||
| chr16:87913665
|
T | C | 71 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0077others(68): Show | 71 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.341-8761A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913665 | ||||||
| chr16:87913667
|
T | C | 17 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(14): Show | 17 | HG01081.hp2 HG01516.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.341-8763A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913667 | ||||||
| chr16:87913820
|
C | G | 23 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(20): Show | 23 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.341-8916G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913820 | ||||||
| chr16:87913934
|
A | G | 57 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0094others(54): Show | 57 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.341-9030T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913934 | ||||||
| chr16:87913943
|
T | C | 274 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0037others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.341-9039A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913943 | ||||||
| chr16:87913956
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.341-9052G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913956 | ||||||
| chr16:87913965
|
C | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0071 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.341-9061G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913965 | ||||||
| chr16:87913966
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.341-9062C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87913966 | ||||||
| chr16:87914001
|
C | T | 32 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0056others(29): Show | 32 | HG00639.hp2 HG01167.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.341-9097G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914001 | ||||||
| chr16:87914177
|
T | C | 14 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0077others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.341-9273A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914177 | ||||||
| chr16:87914237
|
A | G | 1 | a0001c0002t0002g0391 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.341-9333T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914237 | ||||||
| chr16:87914281
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.341-9377A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914281 | ||||||
| chr16:87914349
|
C | T | 1 | a0001c0003t0002g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.341-9445G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914349 | ||||||
| chr16:87914367
|
A | G | 50 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0001g0097others(47): Show | 50 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.341-9463T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914367 | ||||||
| chr16:87914394
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.341-9490A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914394 | ||||||
| chr16:87914405
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.341-9501T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914405 | ||||||
| chr16:87914409
|
A | G | 80 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0038others(77): Show | 80 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.341-9505T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914409 | ||||||
| chr16:87914430
|
G | A | 1 | a0002c0005t0001g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.341-9526C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914430 | ||||||
| chr16:87914441
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.341-9537G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914441 | ||||||
| chr16:87914491
|
C | G | 11 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0122others(8): Show | 11 | HG01891.hp2 HG02486.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.341-9587G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914491 | ||||||
| chr16:87914520
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.341-9616C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914520 | ||||||
| chr16:87914523
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.341-9619C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914523 | ||||||
| chr16:87914607
|
A | T | 163 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(160): Show | 163 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.341-9703T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914607 | ||||||
| chr16:87914609
|
C | G | 163 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(160): Show | 163 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.341-9705G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914609 | ||||||
| chr16:87914657
|
C | G | 1 | a0003c0006t0001g0011 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.341-9753G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914657 | ||||||
| chr16:87914671
|
C | T | 1 | a0001c0002t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.341-9767G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914671 | ||||||
| chr16:87914683
|
G | A | 2 | a0001c0003t0002g0090a0001c0003t0002g0332 | 2 | HG01358.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.341-9779C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914683 | ||||||
| chr16:87914863
|
GGCACAGA others(5): Show |
G | 1 | a0001c0001t0001g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.341-9971_341-9960d others(14): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914863 | ||||||
| chr16:87914875
|
T | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0030others(141): Show | 145 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.341-9971A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914875 | ||||||
| chr16:87914889
|
A | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0029others(281): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.341-9985T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914889 | ||||||
| chr16:87914928
|
G | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.341-10024C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914928 | ||||||
| chr16:87914933
|
G | A | 8 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0112others(5): Show | 8 | HG00642.hp2 HG00735.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.341-10029C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914933 | ||||||
| chr16:87914989
|
G | T | 1 | a0003c0006t0001g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.341-10085C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914989 | ||||||
| chr16:87914997
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.341-10093T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87914997 | ||||||
| chr16:87915055
|
A | G | 37 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(34): Show | 37 | HG00639.hp2 HG01167.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.341-10151T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915055 | ||||||
| chr16:87915059
|
C | A | 29 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(26): Show | 29 | HG00639.hp2 HG01167.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.341-10155G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915059 | ||||||
| chr16:87915101
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.341-10197C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915101 | ||||||
| chr16:87915104
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.341-10200G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915104 | ||||||
| chr16:87915123
|
G | A | 3 | a0001c0001t0001g0336a0001c0002t0002g0260a0001c0003t0002g0257 | 3 | NA18969.hp1 NA18983.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.341-10219C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915123 | ||||||
| chr16:87915131
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.341-10227C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915131 | ||||||
| chr16:87915230
|
C | T | 3 | a0001c0001t0003g0065a0001c0002t0002g0324a0001c0002t0002g0391 | 3 | HG00673.hp1 HG03540.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.341-10326G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915230 | ||||||
| chr16:87915248
|
C | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.341-10344G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915248 | ||||||
| chr16:87915259
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.341-10355G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915259 | ||||||
| chr16:87915343
|
A | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0030others(124): Show | 128 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.341-10439T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915343 | ||||||
| chr16:87915388
|
G | T | 6 | a0001c0001t0001g0062a0001c0001t0001g0077a0001c0001t0001g0231others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-10484C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915388 | ||||||
| chr16:87915456
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.341-10552C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915456 | ||||||
| chr16:87915526
|
A | AT | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(172): Show | 177 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.341-10623dupA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915526 | ||||||
| chr16:87915526
|
A | ATT | 74 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0040others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.341-10624_341-1062 others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915526 | ||||||
| chr16:87915526
|
A | ATTT | 12 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0082others(9): Show | 12 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.341-10625_341-1062 others(7): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915526 | ||||||
| chr16:87915526
|
A | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0182a0001c0001t0001g0375others(4): Show | 7 | HG02300.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-10622T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915526 | ||||||
| chr16:87915526
|
AT | A | 16 | a0001c0001t0001g0062a0001c0001t0001g0068a0001c0001t0001g0077others(13): Show | 16 | HG01069.hp1 HG01081.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.341-10623delA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915526 | ||||||
| chr16:87915526
|
ATTTTT | A | 11 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0234others(8): Show | 11 | HG02258.hp1 HG02615.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.341-10627_341-1062 others(9): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915526 | ||||||
| chr16:87915533
|
T | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0233 | 2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.341-10629A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915533 | ||||||
| chr16:87915535
|
T | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.341-10631A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915535 | ||||||
| chr16:87915621
|
C | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0361a0005c0008t0001g0050 | 3 | HG02647.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.341-10717G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915621 | ||||||
| chr16:87915661
|
C | G | 92 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.341-10757G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915661 | ||||||
| chr16:87915667
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0385 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.341-10763G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915667 | ||||||
| chr16:87915689
|
C | CA | 46 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0085others(43): Show | 46 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.341-10786dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915689 | ||||||
| chr16:87915689
|
CA | C | 8 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0162others(5): Show | 8 | HG02622.hp1 HG02922.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.341-10786delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915689 | ||||||
| chr16:87915689
|
CAA | C | 74 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0045others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.341-10787_341-1078 others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915689 | ||||||
| chr16:87915689
|
CAAA | C | 7 | a0001c0001t0001g0062a0001c0001t0001g0077a0001c0001t0001g0165others(4): Show | 7 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.341-10788_341-1078 others(7): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915689 | ||||||
| chr16:87915698
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0233a0001c0002t0002g0087 | 3 | HG02622.hp1 HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.341-10794T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915698 | ||||||
| chr16:87915699
|
A | G | 74 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0045others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.341-10795T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915699 | ||||||
| chr16:87915700
|
A | G | 2 | a0001c0001t0001g0165a0001c0003t0002g0115 | 2 | HG01069.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.341-10796T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915700 | ||||||
| chr16:87915708
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0188 | 2 | HG00140.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.341-10804T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915708 | ||||||
| chr16:87915779
|
T | C | 5 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0060others(2): Show | 5 | HG02615.hp1 HG03225.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-10875A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915779 | ||||||
| chr16:87915973
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.340+10775C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915973 | ||||||
| chr16:87915974
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.340+10774G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915974 | ||||||
| chr16:87915985
|
C | T | 15 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0072others(12): Show | 15 | HG00673.hp2 HG01167.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.340+10763G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915985 | ||||||
| chr16:87915989
|
A | G | 11 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0072others(8): Show | 11 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.340+10759T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87915989 | ||||||
| chr16:87916004
|
G | C | 3 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG03669.hp2 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.340+10744C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916004 | ||||||
| chr16:87916016
|
G | T | 171 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0029others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.340+10732C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916016 | ||||||
| chr16:87916084
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.340+10664G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916084 | ||||||
| chr16:87916099
|
T | C | 9 | a0001c0001t0001g0064a0001c0001t0001g0137a0001c0001t0001g0149others(6): Show | 9 | HG01074.hp2 HG01255.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.340+10649A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916099 | ||||||
| chr16:87916100
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.340+10648C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916100 | ||||||
| chr16:87916105
|
T | C | 21 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0044others(18): Show | 21 | HG01256.hp1 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.340+10643A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916105 | ||||||
| chr16:87916112
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0043others(28): Show | 32 | HG01993.hp2 HG02132.hp1 HG02523.hp2 others(29): Show |
intron_variant | MODIFIER | c.340+10636C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916112 | ||||||
| chr16:87916122
|
C | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0040others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.340+10626G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916122 | ||||||
| chr16:87916123
|
G | A | 1 | a0001c0003t0002g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.340+10625C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916123 | ||||||
| chr16:87916124
|
C | T | 4 | a0001c0001t0001g0287a0001c0002t0002g0113a0001c0003t0002g0381others(1): Show | 4 | HG02976.hp2 HG03098.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+10624G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916124 | ||||||
| chr16:87916155
|
A | G | 2 | a0001c0001t0001g0154a0002c0010t0002g0018 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.340+10593T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916155 | ||||||
| chr16:87916167
|
C | CA | 40 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0053others(37): Show | 40 | HG00609.hp1 HG01109.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.340+10580dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916167 | ||||||
| chr16:87916167
|
C | CAA | 13 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0047others(10): Show | 13 | HG00639.hp2 HG00642.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.340+10579_340+1058 others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916167 | ||||||
| chr16:87916167
|
C | CAAA | 49 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0038others(46): Show | 49 | HG00438.hp1 HG00673.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.340+10578_340+1058 others(7): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916167 | ||||||
| chr16:87916167
|
C | CAAAA | 8 | a0001c0001t0001g0083a0001c0001t0001g0178a0001c0001t0001g0210others(5): Show | 8 | HG01106.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.340+10577_340+1058 others(8): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916167 | ||||||
| chr16:87916182
|
C | A | 112 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0038others(109): Show | 112 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.340+10566G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916182 | ||||||
| chr16:87916182
|
C | CA | 16 | a0001c0001t0001g0070a0001c0001t0001g0103a0001c0001t0001g0109others(13): Show | 16 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.340+10565dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916182 | ||||||
| chr16:87916257
|
G | C | 2 | a0003c0006t0001g0005a0003c0006t0001g0006 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.340+10491C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916257 | ||||||
| chr16:87916389
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0208a0001c0001t0001g0374 | 3 | HG01175.hp1 HG01175.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.340+10359G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916389 | ||||||
| chr16:87916429
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0362a0001c0001t0003g0065 | 3 | HG00642.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.340+10319C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916429 | ||||||
| chr16:87916509
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.340+10239T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916509 | ||||||
| chr16:87916530
|
G | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0362 | 2 | HG00642.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.340+10218C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916530 | ||||||
| chr16:87916546
|
C | G | 33 | a0001c0001t0001g0027a0001c0001t0001g0060a0001c0001t0001g0061others(30): Show | 33 | HG01074.hp2 HG01243.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.340+10202G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916546 | ||||||
| chr16:87916639
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.340+10109C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916639 | ||||||
| chr16:87916730
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0182 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.340+10018G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916730 | ||||||
| chr16:87916733
|
C | T | 219 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0031others(216): Show | 220 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.340+10015G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916733 | ||||||
| chr16:87916769
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.340+9979G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916769 | ||||||
| chr16:87916785
|
C | T | 218 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0031others(215): Show | 219 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.340+9963G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916785 | ||||||
| chr16:87916898
|
C | T | 1 | a0005c0008t0001g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.340+9850G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916898 | ||||||
| chr16:87916899
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0136 | 2 | HG00140.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.340+9849C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916899 | ||||||
| chr16:87916919
|
A | G | 217 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0031others(214): Show | 218 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.340+9829T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916919 | ||||||
| chr16:87916966
|
G | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0031others(216): Show | 220 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.340+9782C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916966 | ||||||
| chr16:87916992
|
T | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0031others(215): Show | 219 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.340+9756A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87916992 | ||||||
| chr16:87917036
|
C | T | 3 | a0001c0001t0001g0059a0001c0012t0001g0388a0002c0005t0001g0024 | 3 | HG02615.hp1 HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.340+9712G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917036 | ||||||
| chr16:87917091
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0040others(94): Show | 98 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.340+9657G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917091 | ||||||
| chr16:87917092
|
G | A | 6 | a0001c0001t0001g0044a0001c0001t0001g0077a0001c0001t0001g0154others(3): Show | 6 | HG02451.hp1 HG03041.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+9656C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917092 | ||||||
| chr16:87917104
|
C | CA | 31 | a0001c0001t0001g0030a0001c0001t0001g0045a0001c0001t0001g0070others(28): Show | 31 | HG00639.hp2 HG00673.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.340+9643dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917104 | ||||||
| chr16:87917104
|
C | CAA | 25 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0066others(22): Show | 25 | HG01074.hp2 HG01243.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.340+9642_340+9643d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917104 | ||||||
| chr16:87917104
|
CA | C | 27 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0064others(24): Show | 27 | HG00323.hp2 HG01070.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.340+9643delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917104 | ||||||
| chr16:87917111
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.340+9637T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917111 | ||||||
| chr16:87917117
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.340+9631T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917117 | ||||||
| chr16:87917132
|
G | GA | 215 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0037others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.340+9615dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917132 | ||||||
| chr16:87917152
|
T | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0154a0001c0001t0001g0175others(1): Show | 4 | HG03209.hp2 HG03453.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+9596A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917152 | ||||||
| chr16:87917159
|
C | T | 216 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0037others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.340+9589G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917159 | ||||||
| chr16:87917190
|
C | T | 6 | a0001c0001t0001g0037a0001c0001t0001g0066a0001c0001t0001g0287others(3): Show | 6 | HG00639.hp2 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+9558G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917190 | ||||||
| chr16:87917259
|
A | C | 41 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0039others(38): Show | 41 | HG00642.hp1 HG01074.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.340+9489T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917259 | ||||||
| chr16:87917286
|
C | T | 2 | a0001c0002t0002g0073a0001c0002t0002g0076 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.340+9462G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917286 | ||||||
| chr16:87917296
|
G | A | 42 | a0001c0001t0001g0120a0001c0001t0001g0132a0001c0001t0001g0134others(39): Show | 42 | HG00621.hp1 HG00673.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.340+9452C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917296 | ||||||
| chr16:87917424
|
T | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(51): Show | 55 | HG00621.hp2 HG01109.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.340+9324A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917424 | ||||||
| chr16:87917451
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.340+9297C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917451 | ||||||
| chr16:87917564
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.340+9184G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917564 | ||||||
| chr16:87917585
|
C | T | 1 | a0001c0001t0001g0382 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.340+9163G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917585 | ||||||
| chr16:87917586
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.340+9162C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917586 | ||||||
| chr16:87917597
|
T | C | 1 | a0001c0001t0001g0244 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.340+9151A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917597 | ||||||
| chr16:87917606
|
C | A | 220 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0037others(217): Show | 221 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.340+9142G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917606 | ||||||
| chr16:87917615
|
GCACA | G | 10 | a0001c0001t0001g0037a0001c0001t0001g0060a0001c0001t0001g0061others(7): Show | 10 | HG00639.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+9129_340+9132d others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917615 | ||||||
| chr16:87917619
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.340+9129T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917619 | ||||||
| chr16:87917637
|
G | A | 211 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0037others(208): Show | 212 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.340+9111C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917637 | ||||||
| chr16:87917673
|
G | GCA | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(299): Show | 304 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.340+9073_340+9074d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917673 | ||||||
| chr16:87917704
|
AACACACA others(13): Show |
A | 51 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0045others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.340+9024_340+9043d others(22): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917704 | ||||||
| chr16:87917716
|
A | AAC | 15 | a0001c0001t0001g0068a0001c0001t0001g0195a0001c0001t0001g0199others(12): Show | 15 | HG00323.hp2 HG01070.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.340+9030_340+9031d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917716 | ||||||
| chr16:87917717
|
ACACGTGC others(48): Show |
A | 48 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0038others(45): Show | 48 | HG00639.hp2 HG01074.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.340+8976_340+9030d others(57): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917717 | ||||||
| chr16:87917721
|
G | A | 15 | a0001c0001t0001g0068a0001c0001t0001g0195a0001c0001t0001g0199others(12): Show | 15 | HG00323.hp2 HG01070.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.340+9027C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917721 | ||||||
| chr16:87917729
|
A | ATGTATAC others(6): Show |
15 | a0001c0001t0001g0068a0001c0001t0001g0195a0001c0001t0001g0199others(12): Show | 15 | HG00323.hp2 HG01070.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.340+9018_340+9019i others(15): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917729 | ||||||
| chr16:87917734
|
T | C | 1 | a0001c0004t0001g0337 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.340+9014A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917734 | ||||||
| chr16:87917736
|
A | T | 15 | a0001c0001t0001g0068a0001c0001t0001g0195a0001c0001t0001g0199others(12): Show | 15 | HG00323.hp2 HG01070.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.340+9012T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917736 | ||||||
| chr16:87917737
|
A | ACACACAT others(28): Show |
1 | a0001c0001t0001g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.340+8976_340+9010d others(37): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917737 | ||||||
| chr16:87917737
|
A | G | 15 | a0001c0001t0001g0068a0001c0001t0001g0195a0001c0001t0001g0199others(12): Show | 15 | HG00323.hp2 HG01070.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.340+9011T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917737 | ||||||
| chr16:87917737
|
ACACACAT others(28): Show |
A | 100 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(97): Show | 101 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.340+8976_340+9010d others(37): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917737 | ||||||
| chr16:87917756
|
TACACAGT others(30): Show |
T | 5 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 5 | HG01256.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+8955_340+8991d others(39): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917756 | ||||||
| chr16:87917770
|
GTGCACAC others(1): Show |
G | 14 | a0001c0001t0001g0068a0001c0001t0001g0195a0001c0001t0001g0199others(11): Show | 14 | HG00323.hp2 HG01070.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.340+8970_340+8977d others(10): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917770 | ||||||
| chr16:87917789
|
T | A | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.340+8959A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917789 | ||||||
| chr16:87917791
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.340+8957A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917791 | ||||||
| chr16:87917795
|
CAG | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0154a0001c0001t0001g0175others(1): Show | 4 | HG03209.hp2 HG03453.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+8951_340+8952d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917795 | ||||||
| chr16:87917824
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.340+8924G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917824 | ||||||
| chr16:87917869
|
C | G | 1 | a0001c0002t0002g0187 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.340+8879G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917869 | ||||||
| chr16:87917928
|
T | A | 1 | a0001c0001t0001g0146 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.340+8820A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917928 | ||||||
| chr16:87917961
|
T | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(114): Show | 118 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.340+8787A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917961 | ||||||
| chr16:87917971
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.340+8777C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87917971 | ||||||
| chr16:87918056
|
G | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0040others(107): Show | 111 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(108): Show |
intron_variant | MODIFIER | c.340+8692C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918056 | ||||||
| chr16:87918091
|
A | T | 1 | a0001c0001t0001g0327 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.340+8657T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918091 | ||||||
| chr16:87918111
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.340+8637C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918111 | ||||||
| chr16:87918140
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0351 | 2 | HG02056.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.340+8608C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918140 | ||||||
| chr16:87918239
|
C | G | 1 | a0001c0001t0001g0327 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.340+8509G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918239 | ||||||
| chr16:87918274
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.340+8474C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918274 | ||||||
| chr16:87918290
|
G | A | 1 | a0002c0005t0001g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.340+8458C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918290 | ||||||
| chr16:87918330
|
G | A | 2 | a0001c0001t0001g0320a0001c0002t0002g0296 | 2 | HG03688.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.340+8418C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918330 | ||||||
| chr16:87918392
|
C | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0234a0001c0002t0002g0033 | 3 | HG01257.hp1 HG04204.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.340+8356G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918392 | ||||||
| chr16:87918460
|
TG | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0040others(107): Show | 111 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(108): Show |
intron_variant | MODIFIER | c.340+8287delC | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918460 | ||||||
| chr16:87918472
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0040others(111): Show | 115 | HG00140.hp1 HG00621.hp1 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.340+8276A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918472 | ||||||
| chr16:87918559
|
G | C | 3 | a0001c0001t0001g0359a0003c0006t0001g0010a0005c0008t0001g0052 | 3 | HG01109.hp2 HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.340+8189C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918559 | ||||||
| chr16:87918609
|
C | T | 1 | a0001c0001t0003g0384 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.340+8139G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918609 | ||||||
| chr16:87918775
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.340+7973C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918775 | ||||||
| chr16:87918820
|
G | A | 12 | a0001c0001t0001g0027a0001c0001t0001g0289a0001c0001t0001g0290others(9): Show | 12 | HG01243.hp1 HG02258.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.340+7928C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918820 | ||||||
| chr16:87918872
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.340+7876G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918872 | ||||||
| chr16:87918879
|
C | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0040others(111): Show | 115 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(112): Show |
intron_variant | MODIFIER | c.340+7869G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918879 | ||||||
| chr16:87918918
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.340+7830C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918918 | ||||||
| chr16:87918975
|
C | CAAAT | 114 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0040others(111): Show | 115 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(112): Show |
intron_variant | MODIFIER | c.340+7772_340+7773i others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87918975 | ||||||
| chr16:87919116
|
C | T | 1 | a0001c0012t0001g0388 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.340+7632G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919116 | ||||||
| chr16:87919117
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0284a0003c0006t0001g0005others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+7631C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919117 | ||||||
| chr16:87919192
|
T | G | 1 | a0001c0002t0002g0333 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.340+7556A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919192 | ||||||
| chr16:87919284
|
T | C | 3 | a0001c0001t0001g0066a0003c0006t0001g0009a0003c0009t0002g0008 | 3 | HG02109.hp1 HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.340+7464A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919284 | ||||||
| chr16:87919304
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0094others(38): Show | 42 | HG00323.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.340+7444G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919304 | ||||||
| chr16:87919361
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0002t0002g0285others(2): Show | 5 | HG01256.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+7387C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919361 | ||||||
| chr16:87919367
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0394 | 2 | NA18992.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.340+7381G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919367 | ||||||
| chr16:87919417
|
A | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(127): Show | 131 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(128): Show |
intron_variant | MODIFIER | c.340+7331T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919417 | ||||||
| chr16:87919468
|
A | G | 97 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0042others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.340+7280T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919468 | ||||||
| chr16:87919510
|
G | T | 1 | a0001c0001t0001g0198 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.340+7238C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919510 | ||||||
| chr16:87919544
|
T | TCTGGGGG others(22): Show |
1 | a0001c0001t0001g0198 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.340+7175_340+7203d others(31): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919544 | ||||||
| chr16:87919650
|
C | T | 1 | a0001c0002t0002g0204 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.340+7098G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919650 | ||||||
| chr16:87919678
|
C | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0037others(222): Show | 226 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.340+7070G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919678 | ||||||
| chr16:87919705
|
C | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.340+7043G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919705 | ||||||
| chr16:87919724
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.340+7024G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919724 | ||||||
| chr16:87919776
|
T | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0038others(142): Show | 146 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(143): Show |
intron_variant | MODIFIER | c.340+6972A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919776 | ||||||
| chr16:87919786
|
A | G | 140 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0038others(137): Show | 141 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(138): Show |
intron_variant | MODIFIER | c.340+6962T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919786 | ||||||
| chr16:87919925
|
A | G | 18 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.340+6823T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87919925 | ||||||
| chr16:87920113
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.340+6635G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920113 | ||||||
| chr16:87920161
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0003g0065 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.340+6587T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920161 | ||||||
| chr16:87920221
|
C | T | 3 | a0001c0001t0003g0288a0001c0003t0002g0379a0002c0005t0001g0024 | 3 | HG02559.hp1 HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.340+6527G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920221 | ||||||
| chr16:87920310
|
T | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0152 | 2 | HG00408.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.340+6438A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920310 | ||||||
| chr16:87920343
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.340+6405G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920343 | ||||||
| chr16:87920399
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0229 | 2 | HG02735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.340+6349C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920399 | ||||||
| chr16:87920439
|
A | G | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0361others(1): Show | 4 | HG02647.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+6309T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920439 | ||||||
| chr16:87920464
|
C | G | 1 | a0001c0004t0001g0369 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.340+6284G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920464 | ||||||
| chr16:87920499
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.340+6249C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920499 | ||||||
| chr16:87920570
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.340+6178T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920570 | ||||||
| chr16:87920599
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.340+6149A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920599 | ||||||
| chr16:87920620
|
C | CTTATT | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0361 | 3 | HG02647.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.340+6123_340+6127d others(7): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920620 | ||||||
| chr16:87920679
|
G | A | 1 | a0001c0002t0002g0228 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.340+6069C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920679 | ||||||
| chr16:87920707
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.340+6041G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920707 | ||||||
| chr16:87920853
|
G | C | 1 | a0005c0008t0001g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.340+5895C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920853 | ||||||
| chr16:87920961
|
T | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02615.hp1 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+5787A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920961 | ||||||
| chr16:87920996
|
T | G | 1 | a0001c0002t0002g0074 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.340+5752A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87920996 | ||||||
| chr16:87921089
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0361 | 3 | HG02647.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.340+5659C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921089 | ||||||
| chr16:87921149
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.340+5599C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921149 | ||||||
| chr16:87921162
|
C | T | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.340+5586G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921162 | ||||||
| chr16:87921179
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.340+5569A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921179 | ||||||
| chr16:87921244
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.340+5504A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921244 | ||||||
| chr16:87921246
|
T | G | 257 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0029others(254): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.340+5502A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921246 | ||||||
| chr16:87921261
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.340+5487C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921261 | ||||||
| chr16:87921411
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.340+5337T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921411 | ||||||
| chr16:87921439
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.340+5309G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921439 | ||||||
| chr16:87921508
|
T | C | 80 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0057others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.340+5240A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921508 | ||||||
| chr16:87921520
|
G | A | 1 | a0005c0008t0001g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.340+5228C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921520 | ||||||
| chr16:87921582
|
T | C | 1 | a0002c0005t0001g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.340+5166A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921582 | ||||||
| chr16:87921633
|
T | G | 1 | a0001c0002t0002g0391 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.340+5115A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921633 | ||||||
| chr16:87921748
|
C | T | 78 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0057others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.340+5000G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921748 | ||||||
| chr16:87921773
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.340+4975C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921773 | ||||||
| chr16:87921825
|
G | C | 1 | a0002c0005t0001g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.340+4923C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921825 | ||||||
| chr16:87921872
|
A | AT | 170 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0029others(167): Show | 171 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(168): Show |
intron_variant | MODIFIER | c.340+4875dupA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921872 | ||||||
| chr16:87921872
|
A | ATT | 4 | a0001c0001t0001g0060a0001c0001t0001g0064a0001c0001t0001g0298others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+4874_340+4875d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921872 | ||||||
| chr16:87921872
|
A | T | 2 | a0001c0001t0001g0360a0001c0003t0002g0054 | 2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.340+4876T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921872 | ||||||
| chr16:87921875
|
A | ATT | 37 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0091others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.340+4871_340+4872d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921875 | ||||||
| chr16:87921875
|
A | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0029others(178): Show | 182 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(179): Show |
intron_variant | MODIFIER | c.340+4873T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921875 | ||||||
| chr16:87921877
|
TA | T | 23 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0287others(20): Show | 23 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.340+4870delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921877 | ||||||
| chr16:87921878
|
A | ATT | 19 | a0001c0001t0001g0051a0001c0001t0001g0063a0001c0001t0001g0071others(16): Show | 19 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.340+4868_340+4869d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921878 | ||||||
| chr16:87921878
|
A | T | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(347): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.340+4870T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921878 | ||||||
| chr16:87921908
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.340+4840G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921908 | ||||||
| chr16:87921970
|
C | G | 78 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0038others(75): Show | 79 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.340+4778G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921970 | ||||||
| chr16:87921974
|
C | G | 7 | a0001c0001t0001g0088a0001c0001t0001g0122a0001c0001t0001g0364others(4): Show | 7 | HG02486.hp1 HG02895.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+4774G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87921974 | ||||||
| chr16:87922081
|
A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0029others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.340+4667T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922081 | ||||||
| chr16:87922202
|
C | T | 21 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0287others(18): Show | 21 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.340+4546G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922202 | ||||||
| chr16:87922217
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.340+4531C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922217 | ||||||
| chr16:87922295
|
C | T | 1 | a0002c0005t0001g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.340+4453G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922295 | ||||||
| chr16:87922390
|
A | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0039others(80): Show | 84 | HG00140.hp1 HG00323.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.340+4358T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922390 | ||||||
| chr16:87922506
|
G | A | 96 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0055others(93): Show | 96 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.340+4242C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922506 | ||||||
| chr16:87922594
|
G | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0064others(2): Show | 5 | HG02647.hp2 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+4154C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922594 | ||||||
| chr16:87922601
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.340+4147C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922601 | ||||||
| chr16:87922619
|
T | G | 1 | a0001c0001t0001g0377 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.340+4129A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922619 | ||||||
| chr16:87922636
|
C | CA | 5 | a0001c0001t0001g0046a0001c0001t0001g0062a0001c0001t0001g0289others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+4111dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922636 | ||||||
| chr16:87922693
|
C | T | 10 | a0001c0001t0001g0051a0001c0001t0001g0063a0001c0001t0001g0071others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+4055G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922693 | ||||||
| chr16:87922705
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.340+4043C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922705 | ||||||
| chr16:87922743
|
C | G | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.340+4005G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922743 | ||||||
| chr16:87922781
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.340+3967G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922781 | ||||||
| chr16:87922795
|
G | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.340+3953C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922795 | ||||||
| chr16:87922900
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.340+3848C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922900 | ||||||
| chr16:87922953
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.340+3795A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87922953 | ||||||
| chr16:87923032
|
A | T | 8 | a0001c0001t0001g0068a0001c0001t0001g0088a0001c0001t0001g0122others(5): Show | 8 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.340+3716T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923032 | ||||||
| chr16:87923089
|
C | G | 21 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0039others(18): Show | 21 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.340+3659G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923089 | ||||||
| chr16:87923278
|
T | C | 1 | a0001c0001t0001g0318 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.340+3470A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923278 | ||||||
| chr16:87923335
|
T | C | 25 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0072others(22): Show | 25 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.340+3413A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923335 | ||||||
| chr16:87923375
|
A | G | 11 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0121others(8): Show | 11 | HG00639.hp2 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.340+3373T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923375 | ||||||
| chr16:87923390
|
G | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.340+3358C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923390 | ||||||
| chr16:87923468
|
A | G | 1 | a0001c0001t0001g0339 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.340+3280T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923468 | ||||||
| chr16:87923480
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0252 | 2 | NA18980.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.340+3268C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923480 | ||||||
| chr16:87923581
|
G | A | 2 | a0001c0002t0002g0073a0001c0002t0002g0076 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.340+3167C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923581 | ||||||
| chr16:87923615
|
T | C | 1 | a0001c0002t0002g0228 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.340+3133A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923615 | ||||||
| chr16:87923630
|
G | C | 98 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0056others(95): Show | 98 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.340+3118C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923630 | ||||||
| chr16:87923696
|
C | G | 1 | a0005c0008t0001g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.340+3052G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923696 | ||||||
| chr16:87923728
|
A | G | 99 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0056others(96): Show | 99 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.340+3020T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923728 | ||||||
| chr16:87923736
|
C | T | 2 | a0001c0001t0001g0281a0001c0001t0001g0344 | 2 | NA18984.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.340+3012G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923736 | ||||||
| chr16:87923750
|
C | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0064others(2): Show | 5 | HG02647.hp2 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+2998G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923750 | ||||||
| chr16:87923842
|
A | C | 2 | a0001c0001t0001g0382a0001c0002t0002g0087 | 2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.340+2906T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923842 | ||||||
| chr16:87923852
|
T | C | 85 | a0001c0001t0001g0029a0001c0001t0001g0079a0001c0001t0001g0085others(82): Show | 85 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.340+2896A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87923852 | ||||||
| chr16:87924039
|
A | T | 3 | a0001c0001t0001g0298a0001c0001t0001g0335a0001c0013t0001g0321 | 3 | HG01515.hp1 HG02257.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.340+2709T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924039 | ||||||
| chr16:87924142
|
C | A | 197 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0037others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.340+2606G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924142 | ||||||
| chr16:87924215
|
G | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0121 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.340+2533C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924215 | ||||||
| chr16:87924294
|
C | T | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0068others(3): Show | 6 | HG01256.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.340+2454G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924294 | ||||||
| chr16:87924313
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.340+2435T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924313 | ||||||
| chr16:87924341
|
G | A | 64 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0069others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.340+2407C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924341 | ||||||
| chr16:87924345
|
GGA | G | 20 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0072others(17): Show | 20 | HG00639.hp2 HG01243.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.340+2401_340+2402d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924345 | ||||||
| chr16:87924354
|
G | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0104others(52): Show | 56 | HG00140.hp1 HG00621.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.340+2394C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924354 | ||||||
| chr16:87924456
|
G | A | 1 | a0001c0001t0001g0349 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.340+2292C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924456 | ||||||
| chr16:87924466
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.340+2282C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924466 | ||||||
| chr16:87924506
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.340+2242G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924506 | ||||||
| chr16:87924676
|
G | A | 1 | a0002c0005t0001g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.340+2072C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924676 | ||||||
| chr16:87924781
|
A | G | 11 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.340+1967T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924781 | ||||||
| chr16:87924802
|
G | T | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG02015.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.340+1946C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924802 | ||||||
| chr16:87924848
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.340+1900C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924848 | ||||||
| chr16:87924856
|
G | C | 1 | a0001c0001t0001g0234 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.340+1892C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924856 | ||||||
| chr16:87924904
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.340+1844C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924904 | ||||||
| chr16:87924956
|
G | C | 82 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0069others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.340+1792C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87924956 | ||||||
| chr16:87925065
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0089 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.340+1683G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925065 | ||||||
| chr16:87925093
|
C | G | 81 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0064others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.340+1655G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925093 | ||||||
| chr16:87925120
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.340+1628C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925120 | ||||||
| chr16:87925146
|
T | C | 113 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0042others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.340+1602A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925146 | ||||||
| chr16:87925284
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.340+1464G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925284 | ||||||
| chr16:87925317
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.340+1431C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925317 | ||||||
| chr16:87925436
|
C | A | 7 | a0001c0001t0001g0380a0001c0001t0001g0386a0001c0001t0003g0230others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+1312G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925436 | ||||||
| chr16:87925512
|
G | A | 1 | a0001c0001t0001g0341 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.340+1236C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925512 | ||||||
| chr16:87925523
|
C | A | 1 | a0001c0001t0001g0364 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.340+1225G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925523 | ||||||
| chr16:87925670
|
T | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0068others(2): Show | 5 | HG02280.hp1 HG03225.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+1078A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925670 | ||||||
| chr16:87925680
|
C | T | 2 | a0001c0001t0001g0281a0001c0001t0001g0344 | 2 | NA18984.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.340+1068G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925680 | ||||||
| chr16:87925685
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.340+1063C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925685 | ||||||
| chr16:87925757
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.340+991T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925757 | ||||||
| chr16:87925816
|
C | T | 2 | a0001c0001t0001g0085a0001c0003t0002g0086 | 2 | NA18999.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.340+932G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925816 | ||||||
| chr16:87925828
|
G | A | 4 | a0001c0001t0001g0382a0001c0001t0001g0385a0001c0001t0003g0384others(1): Show | 4 | HG02055.hp2 HG02976.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+920C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925828 | ||||||
| chr16:87925902
|
C | G | 88 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0051others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.340+846G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925902 | ||||||
| chr16:87925921
|
G | C | 180 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0044others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.340+827C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925921 | ||||||
| chr16:87925949
|
G | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0304a0001c0001t0001g0305others(4): Show | 7 | HG00408.hp1 HG02080.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+799C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925949 | ||||||
| chr16:87925967
|
A | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG01346.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.340+781T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925967 | ||||||
| chr16:87925977
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.340+771G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87925977 | ||||||
| chr16:87926025
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0373 | 2 | HG00438.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.340+723C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926025 | ||||||
| chr16:87926026
|
C | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0373 | 2 | HG00438.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.340+722G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926026 | ||||||
| chr16:87926027
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0373 | 2 | HG00438.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.340+721T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926027 | ||||||
| chr16:87926043
|
C | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0057others(50): Show | 54 | HG00621.hp1 HG00673.hp1 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.340+705G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926043 | ||||||
| chr16:87926052
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.340+696T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926052 | ||||||
| chr16:87926182
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.340+566C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926182 | ||||||
| chr16:87926221
|
T | TATAAA | 7 | a0001c0001t0001g0221a0001c0001t0001g0360a0001c0001t0001g0361others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+522_340+526dup others(5): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926221 | ||||||
| chr16:87926221
|
T | TATAAAAT others(3): Show |
72 | a0001c0001t0001g0066a0001c0001t0001g0079a0001c0001t0001g0085others(69): Show | 72 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.340+517_340+526dup others(10): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926221 | ||||||
| chr16:87926221
|
T | TATAAAAT others(8): Show |
8 | a0001c0001t0001g0179a0001c0002t0002g0260a0001c0002t0002g0261others(5): Show | 8 | HG02602.hp1 HG03491.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.340+512_340+526dup others(15): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926221 | ||||||
| chr16:87926221
|
T | TATATAAA others(4): Show |
1 | a0001c0003t0002g0185 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.340+526_340+527ins others(11): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926221 | ||||||
| chr16:87926221
|
TATAAA | T | 8 | a0001c0001t0001g0068a0001c0001t0001g0380a0001c0001t0001g0386others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.340+522_340+526del others(5): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926221 | ||||||
| chr16:87926326
|
C | A | 1 | a0001c0001t0001g0178 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.340+422G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926326 | ||||||
| chr16:87926385
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.340+363C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926385 | ||||||
| chr16:87926387
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0003g0065 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.340+361A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926387 | ||||||
| chr16:87926509
|
G | A | 7 | a0001c0001t0001g0380a0001c0001t0001g0386a0001c0001t0003g0230others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+239C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926509 | ||||||
| chr16:87926514
|
T | C | 1 | a0002c0005t0001g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.340+234A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926514 | ||||||
| chr16:87926527
|
G | A | 87 | a0001c0001t0001g0051a0001c0001t0001g0066a0001c0001t0001g0071others(84): Show | 87 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.340+221C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926527 | ||||||
| chr16:87926569
|
C | G | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.340+179G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926569 | ||||||
| chr16:87926592
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.340+156T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926592 | ||||||
| chr16:87926616
|
C | G | 2 | a0001c0001t0001g0064a0001c0001t0003g0065 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.340+132G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926616 | ||||||
| chr16:87926677
|
C | T | 7 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(4): Show | 7 | HG00621.hp1 HG02040.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.340+71G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926677 | ||||||
| chr16:87926727
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0238a0001c0004t0001g0367 | 3 | HG00140.hp1 HG01192.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.340+21G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926727 | ||||||
| chr16:87926728
|
G | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0121 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.340+20C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 2/6 | chr16 | 87926728 | ||||||
| chr16:87926954
|
A | T | 79 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0069others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.143-9T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87926954 | ||||||
| chr16:87927035
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-90G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927035 | ||||||
| chr16:87927112
|
A | G | 5 | a0001c0001t0001g0284a0001c0001t0001g0287a0001c0002t0002g0285others(2): Show | 5 | HG02486.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-167T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927112 | ||||||
| chr16:87927122
|
C | T | 1 | a0001c0014t0001g0102 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.143-177G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927122 | ||||||
| chr16:87927203
|
T | C | 1 | a0001c0002t0002g0387 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.143-258A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927203 | ||||||
| chr16:87927359
|
T | C | 102 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0001g0066others(99): Show | 102 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.143-414A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927359 | ||||||
| chr16:87927448
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG01346.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.143-503C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927448 | ||||||
| chr16:87927511
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0003t0002g0054 | 3 | HG01256.hp1 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.143-566G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927511 | ||||||
| chr16:87927555
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.143-610T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927555 | ||||||
| chr16:87927565
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.143-620G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927565 | ||||||
| chr16:87927566
|
G | A | 1 | a0003c0006t0001g0003 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.143-621C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927566 | ||||||
| chr16:87927602
|
C | G | 9 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0135others(6): Show | 9 | HG01361.hp1 HG01952.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-657G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927602 | ||||||
| chr16:87927666
|
G | C | 5 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-721C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927666 | ||||||
| chr16:87927668
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.143-723G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927668 | ||||||
| chr16:87927744
|
C | T | 2 | a0001c0002t0002g0087a0001c0003t0002g0067 | 2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.143-799G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927744 | ||||||
| chr16:87927856
|
C | CA | 87 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0031others(84): Show | 88 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.143-912dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927856 | ||||||
| chr16:87927856
|
CA | C | 8 | a0001c0001t0001g0053a0001c0001t0001g0186a0001c0001t0001g0275others(5): Show | 8 | HG01081.hp2 HG01243.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.143-912delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927856 | ||||||
| chr16:87927925
|
C | G | 99 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0064others(96): Show | 99 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.143-980G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927925 | ||||||
| chr16:87927938
|
G | T | 1 | a0001c0002t0002g0282 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.143-993C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927938 | ||||||
| chr16:87927966
|
C | G | 1 | a0001c0001t0001g0362 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.143-1021G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927966 | ||||||
| chr16:87927970
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.143-1025G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927970 | ||||||
| chr16:87927971
|
T | G | 200 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0044others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.143-1026A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87927971 | ||||||
| chr16:87928065
|
A | C | 33 | a0001c0001t0001g0037a0001c0001t0001g0088a0001c0001t0001g0195others(30): Show | 33 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.143-1120T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928065 | ||||||
| chr16:87928104
|
C | T | 7 | a0001c0001t0001g0380a0001c0001t0001g0386a0001c0001t0003g0230others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-1159G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928104 | ||||||
| chr16:87928165
|
A | T | 90 | a0001c0001t0001g0051a0001c0001t0001g0066a0001c0001t0001g0071others(87): Show | 90 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.143-1220T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928165 | ||||||
| chr16:87928235
|
A | G | 1 | a0003c0006t0001g0004 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.143-1290T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928235 | ||||||
| chr16:87928266
|
C | T | 20 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0254others(17): Show | 20 | HG00609.hp1 HG00609.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.143-1321G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928266 | ||||||
| chr16:87928267
|
G | T | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.143-1322C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928267 | ||||||
| chr16:87928298
|
G | A | 1 | a0002c0005t0001g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.143-1353C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928298 | ||||||
| chr16:87928364
|
A | G | 9 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0072others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-1419T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928364 | ||||||
| chr16:87928451
|
G | A | 2 | a0001c0001t0003g0288a0002c0005t0001g0024 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.143-1506C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928451 | ||||||
| chr16:87928568
|
T | G | 2 | a0001c0002t0002g0074a0001c0003t0002g0075 | 2 | HG00323.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.143-1623A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928568 | ||||||
| chr16:87928579
|
T | A | 4 | a0001c0001t0001g0201a0001c0001t0001g0239a0001c0001t0001g0269others(1): Show | 4 | HG00099.hp2 HG00741.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-1634A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928579 | ||||||
| chr16:87928604
|
G | C | 1 | a0002c0005t0001g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.143-1659C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928604 | ||||||
| chr16:87928611
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.143-1666C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928611 | ||||||
| chr16:87928655
|
T | C | 3 | a0002c0005t0001g0013a0002c0005t0001g0017a0002c0010t0002g0018 | 3 | HG03195.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.143-1710A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928655 | ||||||
| chr16:87928668
|
T | C | 3 | a0002c0005t0001g0013a0002c0005t0001g0017a0002c0010t0002g0018 | 3 | HG03195.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.143-1723A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928668 | ||||||
| chr16:87928691
|
A | G | 1 | a0002c0005t0001g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.143-1746T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928691 | ||||||
| chr16:87928739
|
CTGGATTA | C | 86 | a0001c0001t0001g0051a0001c0001t0001g0066a0001c0001t0001g0071others(83): Show | 86 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.143-1801_143-1795d others(9): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928739 | ||||||
| chr16:87928739
|
CTGGATTA others(17): Show |
C | 1 | a0001c0001t0001g0362 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.143-1818_143-1795d others(26): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928739 | ||||||
| chr16:87928756
|
CTTTGTTT others(3): Show |
C | 83 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0066others(80): Show | 83 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.143-1821_143-1812d others(12): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928756 | ||||||
| chr16:87928756
|
CTTTGTTT others(4): Show |
C | 2 | a0001c0001t0001g0239a0001c0002t0002g0387 | 2 | HG01993.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.143-1822_143-1812d others(13): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928756 | ||||||
| chr16:87928756
|
CTTTGTTT others(5): Show |
C | 5 | a0001c0001t0001g0072a0001c0001t0001g0382a0001c0001t0001g0385others(2): Show | 5 | HG02055.hp2 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-1823_143-1812d others(14): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928756 | ||||||
| chr16:87928760
|
G | GT | 40 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0039others(37): Show | 40 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.143-1816dupA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928760 | ||||||
| chr16:87928760
|
G | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0064a0001c0001t0003g0065 | 3 | HG03041.hp2 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.143-1815C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928760 | ||||||
| chr16:87928760
|
GT | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(58): Show | 62 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.143-1816delA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928760 | ||||||
| chr16:87928760
|
GTT | G | 60 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0092others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.143-1817_143-1816d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928760 | ||||||
| chr16:87928760
|
GTTTT | G | 6 | a0001c0001t0001g0088a0001c0001t0001g0364a0001c0001t0001g0365others(3): Show | 6 | HG02622.hp1 HG02895.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-1819_143-1816d others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928760 | ||||||
| chr16:87928768
|
T | C | 1 | a0001c0001t0001g0362 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.143-1823A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928768 | ||||||
| chr16:87928773
|
T | C | 1 | a0001c0001t0001g0362 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.143-1828A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928773 | ||||||
| chr16:87928796
|
T | A | 1 | a0005c0008t0001g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.143-1851A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928796 | ||||||
| chr16:87928832
|
C | T | 1 | a0001c0001t0001g0397 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.143-1887G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928832 | ||||||
| chr16:87928837
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.143-1892G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928837 | ||||||
| chr16:87928862
|
A | G | 10 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0064others(7): Show | 10 | HG02055.hp2 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.143-1917T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928862 | ||||||
| chr16:87928873
|
G | T | 1 | a0001c0001t0001g0234 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.143-1928C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928873 | ||||||
| chr16:87928914
|
C | G | 1 | a0003c0006t0001g0003 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.143-1969G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928914 | ||||||
| chr16:87928915
|
G | A | 9 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0072others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-1970C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928915 | ||||||
| chr16:87928917
|
G | A | 5 | a0001c0001t0001g0159a0001c0002t0002g0157a0001c0002t0002g0158others(2): Show | 5 | HG00438.hp2 HG00544.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-1972C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928917 | ||||||
| chr16:87928927
|
C | T | 86 | a0001c0001t0001g0051a0001c0001t0001g0066a0001c0001t0001g0071others(83): Show | 86 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.143-1982G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928927 | ||||||
| chr16:87928970
|
T | C | 394 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(391): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.143-2025A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87928970 | ||||||
| chr16:87929060
|
C | T | 2 | a0001c0001t0001g0044a0002c0005t0001g0016 | 2 | NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.143-2115G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929060 | ||||||
| chr16:87929190
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0057a0001c0003t0002g0381 | 3 | HG02922.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.143-2245C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929190 | ||||||
| chr16:87929279
|
C | G | 2 | a0001c0001t0001g0072a0001c0001t0003g0384 | 2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.143-2334G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929279 | ||||||
| chr16:87929312
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.143-2367G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929312 | ||||||
| chr16:87929344
|
G | C | 88 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0001g0064others(85): Show | 88 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.143-2399C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929344 | ||||||
| chr16:87929451
|
C | CA | 18 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0039others(15): Show | 18 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.143-2507dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929451 | ||||||
| chr16:87929451
|
CA | C | 12 | a0001c0001t0001g0064a0001c0001t0001g0096a0001c0001t0001g0105others(9): Show | 12 | HG00140.hp2 HG02015.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-2507delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929451 | ||||||
| chr16:87929451
|
CAAAA | C | 83 | a0001c0001t0001g0051a0001c0001t0001g0066a0001c0001t0001g0071others(80): Show | 83 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.143-2510_143-2507d others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929451 | ||||||
| chr16:87929493
|
G | C | 1 | a0001c0001t0001g0349 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.143-2548C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929493 | ||||||
| chr16:87929507
|
G | C | 2 | a0001c0001t0001g0360a0001c0001t0001g0361 | 2 | HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.143-2562C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929507 | ||||||
| chr16:87929542
|
T | G | 16 | a0001c0001t0001g0044a0001c0001t0001g0063a0001c0001t0001g0072others(13): Show | 16 | HG02055.hp2 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-2597A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929542 | ||||||
| chr16:87929598
|
T | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-2653A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929598 | ||||||
| chr16:87929601
|
A | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-2656T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929601 | ||||||
| chr16:87929604
|
T | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-2659A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929604 | ||||||
| chr16:87929615
|
A | G | 7 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0122others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-2670T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929615 | ||||||
| chr16:87929632
|
G | T | 7 | a0001c0001t0001g0380a0001c0001t0001g0386a0001c0001t0003g0230others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-2687C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929632 | ||||||
| chr16:87929642
|
G | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0002c0005t0001g0016 | 3 | HG02145.hp2 NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.143-2697C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929642 | ||||||
| chr16:87929643
|
T | C | 50 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(47): Show | 50 | HG00639.hp2 HG01109.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.143-2698A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929643 | ||||||
| chr16:87929648
|
G | A | 1 | a0001c0001t0001g0336 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.143-2703C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929648 | ||||||
| chr16:87929655
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0037others(258): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.143-2710C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929655 | ||||||
| chr16:87929657
|
G | A | 135 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(132): Show | 135 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.143-2712C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929657 | ||||||
| chr16:87929668
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-2723G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929668 | ||||||
| chr16:87929668
|
C | T | 1 | a0003c0006t0001g0003 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.143-2723G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929668 | ||||||
| chr16:87929669
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0037others(137): Show | 141 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.143-2724C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929669 | ||||||
| chr16:87929669
|
G | C | 49 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(46): Show | 49 | HG00639.hp2 HG01109.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.143-2724C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929669 | ||||||
| chr16:87929673
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.143-2728G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929673 | ||||||
| chr16:87929675
|
A | G | 47 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0103others(44): Show | 48 | HG00621.hp1 HG00673.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.143-2730T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929675 | ||||||
| chr16:87929680
|
G | A | 2 | a0001c0003t0002g0185a0001c0012t0001g0388 | 2 | HG01168.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.143-2735C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929680 | ||||||
| chr16:87929683
|
T | C | 3 | a0001c0001t0001g0175a0001c0001t0001g0368a0001c0003t0002g0185 | 3 | HG01099.hp2 HG01168.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.143-2738A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929683 | ||||||
| chr16:87929689
|
C | G | 5 | a0001c0001t0001g0064a0001c0001t0001g0265a0001c0001t0001g0266others(2): Show | 5 | HG03041.hp2 HG03540.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-2744G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929689 | ||||||
| chr16:87929699
|
G | C | 40 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0084others(37): Show | 40 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.143-2754C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929699 | ||||||
| chr16:87929700
|
G | A | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG02015.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.143-2755C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929700 | ||||||
| chr16:87929704
|
C | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG02015.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.143-2759G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929704 | ||||||
| chr16:87929714
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.143-2769A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929714 | ||||||
| chr16:87929722
|
A | T | 1 | a0001c0001t0001g0030 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.143-2777T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929722 | ||||||
| chr16:87929732
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.143-2787G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929732 | ||||||
| chr16:87929734
|
T | C | 1 | a0003c0006t0001g0003 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.143-2789A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929734 | ||||||
| chr16:87929765
|
G | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG00609.hp2 HG02015.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-2820C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929765 | ||||||
| chr16:87929780
|
C | G | 15 | a0001c0001t0001g0079a0001c0001t0001g0171a0001c0001t0001g0175others(12): Show | 15 | HG01243.hp2 HG01261.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.143-2835G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929780 | ||||||
| chr16:87929785
|
T | C | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0072others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.143-2840A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929785 | ||||||
| chr16:87929804
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.143-2859C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929804 | ||||||
| chr16:87929821
|
G | A | 1 | a0003c0006t0001g0003 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.143-2876C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929821 | ||||||
| chr16:87929827
|
G | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0003t0002g0383 | 3 | NA18522.hp1 NA18955.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.143-2882C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929827 | ||||||
| chr16:87929829
|
G | A | 1 | a0001c0002t0001g0249 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.143-2884C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929829 | ||||||
| chr16:87929830
|
C | G | 6 | a0001c0001t0001g0088a0001c0001t0001g0364a0001c0001t0001g0365others(3): Show | 6 | HG02486.hp1 HG02895.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-2885G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929830 | ||||||
| chr16:87929832
|
A | G | 1 | a0001c0012t0001g0388 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.143-2887T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929832 | ||||||
| chr16:87929834
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0002t0002g0087 | 3 | HG02622.hp1 NA18955.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.143-2889G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929834 | ||||||
| chr16:87929851
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.143-2906T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929851 | ||||||
| chr16:87929853
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.143-2908A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929853 | ||||||
| chr16:87929855
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.143-2910G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929855 | ||||||
| chr16:87929867
|
G | A | 1 | a0001c0012t0001g0388 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.143-2922C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929867 | ||||||
| chr16:87929871
|
C | CA | 37 | a0001c0001t0001g0069a0001c0001t0001g0081a0001c0001t0001g0083others(34): Show | 37 | HG00438.hp2 HG01106.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.143-2927dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929871 | ||||||
| chr16:87929871
|
C | CAA | 57 | a0001c0001t0001g0077a0001c0001t0001g0093a0001c0001t0001g0169others(54): Show | 57 | HG00099.hp2 HG00609.hp1 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-2928_143-2927d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929871 | ||||||
| chr16:87929871
|
C | CAAA | 71 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0057others(68): Show | 71 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.143-2929_143-2927d others(5): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929871 | ||||||
| chr16:87929871
|
C | CAAAA | 81 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0038others(78): Show | 82 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.143-2930_143-2927d others(6): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929871 | ||||||
| chr16:87929871
|
C | CAAAAA | 49 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(46): Show | 49 | HG00642.hp1 HG01099.hp2 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.143-2931_143-2927d others(7): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929871 | ||||||
| chr16:87929871
|
CA | C | 12 | a0001c0001t0001g0029a0001c0001t0001g0132a0001c0001t0001g0134others(9): Show | 12 | HG01361.hp1 HG01952.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-2927delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929871 | ||||||
| chr16:87929886
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.143-2941T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929886 | ||||||
| chr16:87929897
|
T | A | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.143-2952A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929897 | ||||||
| chr16:87929930
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.143-2985T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929930 | ||||||
| chr16:87929982
|
G | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0362 | 3 | HG01167.hp2 HG01169.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.143-3037C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929982 | ||||||
| chr16:87929997
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.143-3052C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87929997 | ||||||
| chr16:87930069
|
T | C | 1 | a0001c0003t0002g0381 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.143-3124A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930069 | ||||||
| chr16:87930104
|
C | T | 1 | a0001c0001t0001g0382 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.143-3159G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930104 | ||||||
| chr16:87930109
|
A | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0055others(71): Show | 75 | HG00140.hp2 HG00621.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.143-3164T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930109 | ||||||
| chr16:87930110
|
T | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02280.hp1 HG02615.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-3165A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930110 | ||||||
| chr16:87930157
|
C | T | 14 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0056others(11): Show | 14 | HG01256.hp1 HG02109.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.143-3212G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930157 | ||||||
| chr16:87930160
|
C | G | 21 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0179others(18): Show | 21 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-3215G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930160 | ||||||
| chr16:87930229
|
G | C | 2 | a0001c0001t0003g0288a0002c0005t0001g0024 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.143-3284C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930229 | ||||||
| chr16:87930334
|
C | T | 7 | a0001c0001t0001g0380a0001c0001t0001g0386a0001c0001t0003g0230others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-3389G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930334 | ||||||
| chr16:87930642
|
C | T | 1 | a0001c0002t0002g0211 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.143-3697G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930642 | ||||||
| chr16:87930683
|
G | A | 1 | a0001c0001t0001g0396 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.143-3738C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930683 | ||||||
| chr16:87930706
|
G | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0056others(3): Show | 6 | HG01256.hp1 HG02572.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-3761C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930706 | ||||||
| chr16:87930735
|
AT | A | 196 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0038others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.143-3791delA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930735 | ||||||
| chr16:87930735
|
ATT | A | 20 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0127others(17): Show | 20 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.143-3792_143-3791d others(4): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930735 | ||||||
| chr16:87930751
|
TC | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0128others(40): Show | 44 | HG00673.hp1 HG01358.hp2 HG01515.hp1 others(41): Show |
intron_variant | MODIFIER | c.143-3807delG | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930751 | ||||||
| chr16:87930752
|
C | T | 16 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0088others(13): Show | 16 | HG00621.hp1 HG00621.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.143-3807G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930752 | ||||||
| chr16:87930810
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0055others(61): Show | 65 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.143-3865T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930810 | ||||||
| chr16:87930877
|
G | A | 1 | a0001c0001t0001g0359 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.143-3932C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930877 | ||||||
| chr16:87930891
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0101 | 3 | HG00642.hp2 HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.143-3946G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930891 | ||||||
| chr16:87930964
|
C | A | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-4019G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930964 | ||||||
| chr16:87930981
|
T | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.143-4036A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87930981 | ||||||
| chr16:87931111
|
A | AT | 8 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0001g0129others(5): Show | 8 | HG02486.hp1 HG03669.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.143-4167dupA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931111 | ||||||
| chr16:87931111
|
AT | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0084others(48): Show | 52 | HG00621.hp1 HG00673.hp1 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.143-4167delA | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931111 | ||||||
| chr16:87931198
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0058 | 3 | NA18975.hp2 NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.143-4253C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931198 | ||||||
| chr16:87931205
|
G | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0055others(57): Show | 61 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.143-4260C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931205 | ||||||
| chr16:87931364
|
G | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0055others(57): Show | 61 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.143-4419C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931364 | ||||||
| chr16:87931439
|
C | A | 1 | a0003c0006t0001g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.143-4494G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931439 | ||||||
| chr16:87931587
|
A | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0174a0001c0001t0001g0176others(43): Show | 47 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.143-4642T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931587 | ||||||
| chr16:87931615
|
T | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0364a0001c0001t0001g0365others(4): Show | 7 | HG02486.hp1 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-4670A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931615 | ||||||
| chr16:87931670
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.142+4639T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931670 | ||||||
| chr16:87931721
|
A | C | 6 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0307others(3): Show | 6 | HG00408.hp1 HG02080.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+4588T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931721 | ||||||
| chr16:87931735
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0003g0065 | 3 | HG02109.hp1 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.142+4574G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931735 | ||||||
| chr16:87931757
|
C | T | 1 | a0001c0002t0001g0249 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.142+4552G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931757 | ||||||
| chr16:87931768
|
A | G | 287 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0037others(284): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.142+4541T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931768 | ||||||
| chr16:87931949
|
GCCTCTCT others(32): Show |
G | 47 | a0001c0001t0001g0002a0001c0001t0001g0174a0001c0001t0001g0176others(44): Show | 48 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.142+4321_142+4359d others(41): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87931949 | ||||||
| chr16:87932039
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | NA18959.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.142+4270T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932039 | ||||||
| chr16:87932063
|
G | C | 1 | a0001c0001t0001g0234 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.142+4246C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932063 | ||||||
| chr16:87932106
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.142+4203G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932106 | ||||||
| chr16:87932138
|
G | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0174a0001c0001t0001g0175others(46): Show | 50 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.142+4171C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932138 | ||||||
| chr16:87932144
|
C | G | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.142+4165G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932144 | ||||||
| chr16:87932195
|
C | G | 17 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0056others(14): Show | 17 | HG01256.hp1 HG02109.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.142+4114G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932195 | ||||||
| chr16:87932202
|
C | A | 3 | a0003c0006t0001g0007a0003c0006t0001g0009a0003c0006t0001g0010 | 3 | HG02258.hp2 HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.142+4107G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932202 | ||||||
| chr16:87932222
|
A | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(97): Show | 101 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.142+4087T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932222 | ||||||
| chr16:87932331
|
C | G | 1 | a0001c0003t0002g0248 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.142+3978G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932331 | ||||||
| chr16:87932444
|
G | A | 1 | a0001c0012t0001g0388 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.142+3865C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932444 | ||||||
| chr16:87932481
|
C | T | 8 | a0001c0001t0001g0380a0001c0001t0001g0382a0001c0001t0001g0385others(5): Show | 8 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.142+3828G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932481 | ||||||
| chr16:87932537
|
T | C | 16 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0175others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.142+3772A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932537 | ||||||
| chr16:87932557
|
T | G | 83 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0051others(80): Show | 84 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.142+3752A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932557 | ||||||
| chr16:87932808
|
C | G | 77 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0079others(74): Show | 77 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.142+3501G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932808 | ||||||
| chr16:87932854
|
A | G | 3 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0009t0002g0008 | 3 | HG02258.hp2 HG02896.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.142+3455T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932854 | ||||||
| chr16:87932952
|
G | A | 8 | a0001c0001t0001g0042a0001c0001t0001g0072a0001c0001t0001g0077others(5): Show | 8 | HG00323.hp2 HG01070.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.142+3357C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932952 | ||||||
| chr16:87932960
|
C | T | 7 | a0001c0001t0001g0380a0001c0001t0001g0382a0001c0001t0001g0385others(4): Show | 7 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+3349G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932960 | ||||||
| chr16:87932961
|
T | G | 7 | a0001c0001t0001g0380a0001c0001t0001g0382a0001c0001t0001g0385others(4): Show | 7 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+3348A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932961 | ||||||
| chr16:87932989
|
C | T | 2 | a0001c0001t0001g0302a0001c0002t0002g0247 | 2 | NA18747.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.142+3320G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87932989 | ||||||
| chr16:87933020
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0291 | 2 | HG01081.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.142+3289G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933020 | ||||||
| chr16:87933055
|
C | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(225): Show | 229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.142+3254G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933055 | ||||||
| chr16:87933098
|
G | C | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.142+3211C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933098 | ||||||
| chr16:87933099
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.142+3210C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933099 | ||||||
| chr16:87933298
|
G | A | 3 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0009t0002g0008 | 3 | HG02258.hp2 HG02896.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.142+3011C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933298 | ||||||
| chr16:87933300
|
T | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02145.hp2 HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.142+3009A>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933300 | ||||||
| chr16:87933488
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.142+2821C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933488 | ||||||
| chr16:87933558
|
T | TC | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0012t0001g0388 | 3 | HG03225.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.142+2750_142+2751i others(3): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933558 | ||||||
| chr16:87933599
|
T | C | 48 | a0001c0001t0001g0079a0001c0001t0001g0235a0001c0001t0001g0236others(45): Show | 48 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.142+2710A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933599 | ||||||
| chr16:87933647
|
C | T | 140 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(137): Show | 141 | HG00323.hp2 HG00408.hp1 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.142+2662G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933647 | ||||||
| chr16:87933659
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.142+2650A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933659 | ||||||
| chr16:87933662
|
A | C | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0003t0002g0086 | 3 | NA18999.hp1 NA19056.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.142+2647T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933662 | ||||||
| chr16:87933846
|
T | A | 2 | a0001c0001t0001g0280a0001c0004t0001g0279 | 2 | HG02523.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.142+2463A>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933846 | ||||||
| chr16:87933886
|
T | C | 4 | a0003c0006t0001g0004a0003c0006t0001g0005a0003c0006t0001g0006others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+2423A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933886 | ||||||
| chr16:87933930
|
TG | T | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0066others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+2378delC | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933930 | ||||||
| chr16:87933939
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0294a0001c0001t0001g0298others(85): Show | 89 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.142+2370C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87933939 | ||||||
| chr16:87934015
|
A | G | 18 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(15): Show | 18 | HG00642.hp1 HG01257.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.142+2294T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934015 | ||||||
| chr16:87934094
|
G | A | 5 | a0003c0006t0001g0003a0003c0006t0001g0004a0003c0006t0001g0005others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+2215C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934094 | ||||||
| chr16:87934125
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.142+2184C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934125 | ||||||
| chr16:87934156
|
G | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+2153C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934156 | ||||||
| chr16:87934209
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0363 | 3 | HG00280.hp1 HG00738.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.142+2100G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934209 | ||||||
| chr16:87934313
|
A | T | 1 | a0001c0001t0001g0078 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.142+1996T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934313 | ||||||
| chr16:87934339
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.142+1970G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934339 | ||||||
| chr16:87934402
|
C | G | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0066others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+1907G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934402 | ||||||
| chr16:87934411
|
A | T | 1 | a0001c0001t0001g0081 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.142+1898T>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934411 | ||||||
| chr16:87934425
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040 | 3 | HG00642.hp1 HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.142+1884C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934425 | ||||||
| chr16:87934458
|
C | G | 18 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(15): Show | 18 | HG00642.hp1 HG01257.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.142+1851G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934458 | ||||||
| chr16:87934533
|
C | T | 1 | a0001c0003t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142+1776G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934533 | ||||||
| chr16:87934542
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.142+1767G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934542 | ||||||
| chr16:87934654
|
G | T | 7 | a0001c0001t0001g0380a0001c0001t0001g0382a0001c0001t0001g0385others(4): Show | 7 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+1655C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934654 | ||||||
| chr16:87934742
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0294a0001c0001t0001g0298others(86): Show | 90 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.142+1567G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934742 | ||||||
| chr16:87934950
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.142+1359T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934950 | ||||||
| chr16:87934952
|
C | A | 9 | a0003c0006t0001g0003a0003c0006t0001g0004a0003c0006t0001g0005others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+1357G>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87934952 | ||||||
| chr16:87935006
|
C | T | 17 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(14): Show | 17 | HG00642.hp1 HG01257.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.142+1303G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935006 | ||||||
| chr16:87935012
|
G | T | 9 | a0003c0006t0001g0003a0003c0006t0001g0004a0003c0006t0001g0005others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+1297C>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935012 | ||||||
| chr16:87935121
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142+1188G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935121 | ||||||
| chr16:87935187
|
T | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(158): Show | 162 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.142+1122A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935187 | ||||||
| chr16:87935279
|
G | C | 1 | a0001c0001t0001g0283 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.142+1030C>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935279 | ||||||
| chr16:87935333
|
G | A | 8 | a0001c0001t0001g0284a0001c0001t0001g0287a0001c0001t0001g0289others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.142+976C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935333 | ||||||
| chr16:87935413
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.142+896C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935413 | ||||||
| chr16:87935475
|
T | C | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0066others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+834A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935475 | ||||||
| chr16:87935493
|
G | A | 1 | a0001c0004t0001g0357 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.142+816C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935493 | ||||||
| chr16:87935523
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.142+786G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935523 | ||||||
| chr16:87935543
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.142+766C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935543 | ||||||
| chr16:87935587
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.142+722C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935587 | ||||||
| chr16:87935603
|
C | T | 9 | a0003c0006t0001g0003a0003c0006t0001g0004a0003c0006t0001g0005others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+706G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935603 | ||||||
| chr16:87935637
|
A | C | 2 | a0001c0001t0001g0294a0001c0002t0002g0295 | 2 | NA18979.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.142+672T>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935637 | ||||||
| chr16:87935862
|
C | G | 4 | a0003c0006t0001g0004a0003c0006t0001g0005a0003c0006t0001g0006others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+447G>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935862 | ||||||
| chr16:87935899
|
G | A | 31 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(28): Show | 31 | HG00323.hp2 HG01070.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.142+410C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935899 | ||||||
| chr16:87935954
|
C | T | 1 | a0001c0002t0002g0387 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.142+355G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935954 | ||||||
| chr16:87935960
|
T | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0063others(104): Show | 108 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.142+349A>G | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935960 | ||||||
| chr16:87935989
|
A | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0294a0001c0001t0001g0298others(86): Show | 90 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.142+320T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87935989 | ||||||
| chr16:87936045
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(157): Show | 161 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.142+264T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87936045 | ||||||
| chr16:87936079
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0294a0001c0001t0001g0298others(86): Show | 90 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.142+230C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87936079 | ||||||
| chr16:87936101
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0294others(103): Show | 107 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.142+208T>C | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87936101 | ||||||
| chr16:87936138
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0003t0002g0054 | 3 | HG01256.hp1 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.142+171G>A | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87936138 | ||||||
| chr16:87936171
|
T | TA | 94 | a0001c0001t0001g0002a0001c0001t0001g0294a0001c0001t0001g0298others(91): Show | 95 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.142+137dupT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87936171 | ||||||
| chr16:87936171
|
T | TAA | 31 | a0001c0001t0001g0380a0001c0001t0001g0382a0001c0001t0001g0385others(28): Show | 31 | HG00639.hp2 HG01192.hp1 HG01981.hp2 others(28): Show |
intron_variant | MODIFIER | c.142+136_142+137dup others(2): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87936171 | ||||||
| chr16:87936171
|
TA | T | 29 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(26): Show | 29 | HG00642.hp1 HG01169.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.142+137delT | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87936171 | ||||||
| chr16:87936192
|
G | A | 13 | a0002c0005t0001g0012a0002c0005t0001g0013a0002c0005t0001g0014others(10): Show | 13 | HG00639.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+117C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87936192 | ||||||
| chr16:87936245
|
G | A | 13 | a0002c0005t0001g0012a0002c0005t0001g0013a0002c0005t0001g0014others(10): Show | 13 | HG00639.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+64C>T | CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 1/6 | chr16 | 87936245 |