Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10225 |
|---|---|
| ensemblid | ENSG00000153283.13 |
| hgncid | 16892 |
| symbol | CD96 |
| name | CD96 molecule |
| refseq_nuc | NM_005816.5 |
| refseq_prot | NP_005807.1 |
| ensembl_nuc | ENST00000352690.9 |
| ensembl_prot | ENSP00000342040.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 111542197 |
| end | 111652372 |
| strand | + |
| ver | v1.2 |
| region | chr3:111542197-111652372 |
| region5000 | chr3:111537197-111657372 |
| regionname0 | CD96_chr3_111542197_111652372 |
| regionname5000 | CD96_chr3_111537197_111657372 |
| 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 | 569 | 271 | 71 | 51 | 101 | 14 | 32 | 80 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0002 | 0/0 | 569 | 21 | 1 | 1 | 17 | 0 | 2 | 12 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0003 | 0/0 | 569 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0004 | 0/0 | 569 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0005 | 0/0 | 569 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0006 | 0/0 | 569 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0007 | 0/0 | 569 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0008 | 0/0 | 569 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1710 | 255 | 63 | 48 | 100 | 12 | 32 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0002 | 0/0 | 1710 | 21 | 1 | 1 | 17 | 0 | 2 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0003 | 0/0 | 1710 | 4 | 3 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0004 | 0/1 | 1710 | 4 | 0 | 1 | 0 | 2 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0005 | 1/0 | 1710 | 4 | 3 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0006 | 0/0 | 1710 | 3 | 3 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0007 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0008 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0009 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0010 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0011 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0012 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0013 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0014 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| c0015 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2619 | 159 | 20 | 31 | 79 | 8 | 21 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0002 | 0/0 | 2618 | 48 | 10 | 5 | 27 | 0 | 6 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0003 | 0/0 | 2619 | 16 | 13 | 0 | 2 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0004 | 0/0 | 2618 | 14 | 1 | 7 | 2 | 1 | 3 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0005 | 0/0 | 2618 | 12 | 10 | 2 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0006 | 1/0 | 2619 | 11 | 6 | 1 | 1 | 0 | 2 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0007 | 0/1 | 2619 | 7 | 1 | 3 | 0 | 2 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0008 | 0/0 | 2619 | 6 | 0 | 4 | 0 | 2 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0009 | 0/0 | 2619 | 4 | 3 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0010 | 0/0 | 2619 | 4 | 0 | 0 | 4 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0011 | 0/0 | 2619 | 2 | 2 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0012 | 0/0 | 2619 | 2 | 0 | 0 | 2 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0013 | 0/0 | 2619 | 2 | 2 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0014 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0015 | 0/0 | 2619 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0016 | 0/0 | 2619 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0017 | 0/0 | 2619 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0018 | 0/0 | 2619 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0019 | 0/0 | 2619 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0020 | 0/0 | 2618 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0021 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0022 | 0/0 | 2660 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0023 | 0/0 | 2644 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0024 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0025 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| t0026 | 0/0 | 2618 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1710 | 255 | 63 | 48 | 100 | 12 | 32 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0003 | 0/0 | 1710 | 4 | 3 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0004 | 0/1 | 1710 | 4 | 0 | 1 | 0 | 2 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0005 | 1/0 | 1710 | 4 | 3 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0011 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0012 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0014 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0015 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0002c0002 | 0/0 | 1710 | 21 | 1 | 1 | 17 | 0 | 2 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0003c0006 | 0/0 | 1710 | 3 | 3 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0004c0009 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0005c0013 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0006c0010 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0007c0008 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0008c0007 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4328 | 140 | 16 | 29 | 67 | 8 | 20 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0002 | 0/0 | 4327 | 37 | 9 | 3 | 19 | 0 | 6 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0003 | 0/0 | 4328 | 14 | 11 | 0 | 2 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0004 | 0/0 | 4327 | 14 | 1 | 7 | 2 | 1 | 3 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0005 | 0/0 | 4327 | 11 | 9 | 2 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0006 | 0/0 | 4328 | 5 | 2 | 1 | 1 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0007 | 0/0 | 4328 | 2 | 1 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0008 | 0/0 | 4328 | 6 | 0 | 4 | 0 | 2 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0009 | 0/0 | 4328 | 4 | 3 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0010 | 0/0 | 4328 | 4 | 0 | 0 | 4 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0011 | 0/0 | 4328 | 2 | 2 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0012 | 0/0 | 4328 | 2 | 0 | 0 | 2 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0013 | 0/0 | 4328 | 2 | 2 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0014 | 0/0 | 4328 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0015 | 0/0 | 4328 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0016 | 0/0 | 4328 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0017 | 0/0 | 4328 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0018 | 0/0 | 4328 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0019 | 0/0 | 4328 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0020 | 0/0 | 4327 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0021 | 0/0 | 4328 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0022 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0023 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0024 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0001t0025 | 0/0 | 4328 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0003t0001 | 0/0 | 4328 | 4 | 3 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0004t0007 | 0/1 | 4328 | 4 | 0 | 1 | 0 | 2 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0005t0006 | 1/0 | 4328 | 4 | 3 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0011t0026 | 0/0 | 4327 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0012t0006 | 0/0 | 4328 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0014t0001 | 0/0 | 4328 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0001c0015t0001 | 0/0 | 4328 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0002c0002t0001 | 0/0 | 4328 | 10 | 0 | 0 | 9 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0002c0002t0002 | 0/0 | 4327 | 10 | 1 | 1 | 8 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0002c0002t0006 | 0/0 | 4328 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0003c0006t0003 | 0/0 | 4328 | 2 | 2 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0003c0006t0005 | 0/0 | 4327 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0004c0009t0001 | 0/0 | 4328 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0005c0013t0001 | 0/0 | 4328 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0006c0010t0007 | 0/0 | 4328 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0007c0008t0001 | 0/0 | 4328 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| a0008c0007t0002 | 0/0 | 4327 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | copy fasta | chr3 | 111537197 | 111657372 |
| 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 | 3 | 0 | 3 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0006g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0008g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0008g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0008g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0008g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0009g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0009g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0010g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0010g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0010g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0010g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0011g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0012g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0013g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0013g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0014g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0015g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0016g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0017g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0018g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0019g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0020g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0021g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0022g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0023g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0024g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0025g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0004t0007g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0004t0007g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0004t0007g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0004t0007g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0005t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0005t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0005t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0005t0006g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0011t0026g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0012t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0014t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0015t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0006g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0003c0006t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0003c0006t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0003c0006t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0004c0009t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0005c0013t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0006c0010t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0007c0008t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0008c0007t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0007 | g0239 | EUR | GBR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | GBR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00140 | hp2 | a0001 | c0001 | t0008 | g0009 | EUR | GBR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | FIN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00280 | hp2 | a0001 | c0004 | t0007 | g0238 | EUR | FIN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00323 | hp1 | a0001 | c0001 | t0008 | g0264 | EUR | FIN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | FIN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00733 | hp1 | a0001 | c0001 | t0008 | g0009 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0187 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0200 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0194 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01081 | hp2 | a0001 | c0004 | t0007 | g0237 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0157 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0071 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0265 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01192 | hp2 | a0001 | c0001 | t0009 | g0049 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0070 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01255 | hp1 | a0001 | c0014 | t0001 | g0095 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01255 | hp2 | a0006 | c0010 | t0007 | g0222 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0156 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01261 | hp1 | a0001 | c0001 | t0008 | g0270 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0162 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0143 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | IBS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01978 | hp1 | a0008 | c0007 | t0002 | g0022 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0149 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0065 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02055 | hp2 | a0001 | c0001 | t0023 | g0057 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02074 | hp1 | a0001 | c0001 | t0012 | g0008 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02080 | hp1 | a0001 | c0001 | t0012 | g0008 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02165 | hp1 | a0001 | c0001 | t0010 | g0019 | EAS | CDX | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | CDX | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02257 | hp1 | a0001 | c0001 | t0025 | g0015 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02280 | hp2 | a0003 | c0006 | t0003 | g0165 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0164 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0283 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02451 | hp2 | a0001 | c0001 | t0024 | g0058 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02622 | hp1 | a0001 | c0005 | t0006 | g0060 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0198 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0050 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0185 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0146 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0040 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02818 | hp2 | a0001 | c0001 | t0021 | g0061 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02895 | hp2 | a0001 | c0011 | t0026 | g0036 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0204 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0193 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03041 | hp2 | a0007 | c0008 | t0001 | g0034 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03139 | hp1 | a0003 | c0006 | t0003 | g0167 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0188 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0062 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0190 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03209 | hp1 | a0001 | c0001 | t0020 | g0042 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03209 | hp2 | a0001 | c0012 | t0006 | g0064 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03225 | hp1 | a0003 | c0006 | t0005 | g0166 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03453 | hp1 | a0001 | c0001 | t0014 | g0059 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0067 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03486 | hp2 | a0001 | c0005 | t0006 | g0150 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0073 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0153 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03669 | hp2 | a0002 | c0002 | t0006 | g0021 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0230 | SAS | STU | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0032 | SAS | BEB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG04228 | hp1 | a0001 | c0001 | t0018 | g0133 | SAS | STU | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | YRI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0051 | AFR | YRI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18939 | hp2 | a0001 | c0015 | t0001 | g0119 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18953 | hp1 | a0001 | c0001 | t0010 | g0105 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18961 | hp1 | a0001 | c0001 | t0017 | g0102 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0201 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18971 | hp1 | a0001 | c0001 | t0015 | g0254 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19002 | hp2 | a0004 | c0009 | t0001 | g0243 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0130 | AFR | LWK | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0191 | AFR | LWK | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19058 | hp2 | a0005 | c0013 | t0001 | g0276 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19060 | hp2 | a0001 | c0001 | t0016 | g0087 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19077 | hp1 | a0001 | c0001 | t0010 | g0046 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19088 | hp1 | a0001 | c0001 | t0010 | g0099 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | YRI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19240 | hp2 | a0001 | c0005 | t0006 | g0151 | AFR | YRI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0159 | EUR | TSI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0287 | EUR | TSI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA20805 | hp1 | a0001 | c0001 | t0019 | g0114 | EUR | TSI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | TSI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0163 | SAS | GIH | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | GIH | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0047 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0279 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0172 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | USA | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | USA | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | LWK | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA21309 | hp2 | a0001 | c0001 | t0022 | g0044 | AFR | LWK | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0007 | g0101 | REF | REF | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| homoSapiens_grch38 | hp1 | a0001 | c0005 | t0006 | g0152 | REF | REF | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:111567528
|
G | C | 3 | a0002a0007a0008 | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
missense_variant | MODERATE | c.424G>C | p.Ala142Pro | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/14 | 476/4328 | 424/1710 | 142/569 | chr3 | 111567528 | ||
| chr3:111579061
|
A | C | 2 | a0003a0007 | 4 | HG02280.hp2 HG03041.hp2 HG03139.hp1 others(1): Show |
missense_variant | MODERATE | c.578A>C | p.Gln193Pro | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/14 | 630/4328 | 578/1710 | 193/569 | chr3 | 111579061 | ||
| chr3:111600797
|
G | A | 1 | a0004 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.970G>A | p.Val324Ile | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/14 | 1022/4328 | 970/1710 | 324/569 | chr3 | 111600797 | ||
| chr3:111623777
|
A | T | 1 | a0005 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.1204A>T | p.Thr402Ser | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 9/14 | 1256/4328 | 1204/1710 | 402/569 | chr3 | 111623777 | ||
| chr3:111637205
|
G | A | 1 | a0008 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.1331G>A | p.Arg444Gln | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/14 | 1383/4328 | 1331/1710 | 444/569 | chr3 | 111637205 | ||
| chr3:111638124
|
C | A | 1 | a0006 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1433C>A | p.Thr478Lys | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/14 | 1485/4328 | 1433/1710 | 478/569 | chr3 | 111638124 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:111579152
|
C | T | 1 | a0001c0015 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.669C>T | p.Phe223Phe | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/14 | 721/4328 | 669/1710 | 223/569 | chr3 | 111579152 | ||
| chr3:111600793
|
A | G | 1 | a0001c0014 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.966A>G | p.Thr322Thr | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/14 | 1018/4328 | 966/1710 | 322/569 | chr3 | 111600793 | ||
| chr3:111637236
|
G | C | 13 | a0001c0001a0001c0003a0001c0004others(10): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
synonymous_variant | LOW | c.1362G>C | p.Pro454Pro | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/14 | 1414/4328 | 1362/1710 | 454/569 | chr3 | 111637236 | ||
| chr3:111637245
|
A | G | 1 | a0001c0004 | 4 | HG00099.hp1 HG00280.hp2 HG01081.hp2 others(1): Show |
synonymous_variant | LOW | c.1371A>G | p.Ala457Ala | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/14 | 1423/4328 | 1371/1710 | 457/569 | chr3 | 111637245 | ||
| chr3:111638083
|
T | C | 1 | a0001c0012 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1392T>C | p.Asn464Asn | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/14 | 1444/4328 | 1392/1710 | 464/569 | chr3 | 111638083 | ||
| chr3:111647649
|
T | C | 1 | a0001c0011 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.1584T>C | p.Cys528Cys | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/14 | 1636/4328 | 1584/1710 | 528/569 | chr3 | 111647649 | ||
| chr3:111649767
|
C | T | 1 | a0001c0003 | 4 | HG01081.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
synonymous_variant | LOW | c.1671C>T | p.Asn557Asn | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1723/4328 | 1671/1710 | 557/569 | chr3 | 111649767 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:111649966
|
C | T | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(15): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*160C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 160 | chr3 | 111649966 | |||||
| chr3:111650241
|
C | T | 3 | a0001c0001t0007a0001c0004t0007a0006c0010t0007 | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*435C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 435 | chr3 | 111650241 | |||||
| chr3:111650337
|
A | G | 1 | a0001c0001t0008 | 6 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*531A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 531 | chr3 | 111650337 | |||||
| chr3:111650423
|
A | T | 1 | a0001c0001t0013 | 2 | HG02055.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*617A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 617 | chr3 | 111650423 | |||||
| chr3:111650626
|
A | G | 35 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(32): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*820A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 820 | chr3 | 111650626 | |||||
| chr3:111650730
|
A | C | 1 | a0001c0011t0026 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*924A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 924 | chr3 | 111650730 | |||||
| chr3:111650922
|
C | A | 1 | a0001c0001t0012 | 2 | HG02074.hp1 HG02080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1116C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1116 | chr3 | 111650922 | |||||
| chr3:111651136
|
T | G | 1 | a0001c0001t0014 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1330T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1330 | chr3 | 111651136 | |||||
| chr3:111651329
|
G | A | 1 | a0001c0001t0015 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1523G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1523 | chr3 | 111651329 | |||||
| chr3:111651345
|
G | T | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(16): Show | 94 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1539G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1539 | chr3 | 111651345 | |||||
| chr3:111651359
|
C | T | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*1553C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1553 | chr3 | 111651359 | |||||
| chr3:111651609
|
G | A | 2 | a0001c0001t0012a0001c0001t0015 | 3 | HG02074.hp1 HG02080.hp1 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1803G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1803 | chr3 | 111651609 | |||||
| chr3:111651621
|
G | A | 2 | a0001c0001t0010a0001c0001t0020 | 5 | HG02165.hp1 HG03209.hp1 NA18953.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1815G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1815 | chr3 | 111651621 | |||||
| chr3:111651679
|
G | A | 2 | a0001c0001t0011a0001c0001t0021 | 3 | HG02559.hp2 HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1873G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1873 | chr3 | 111651679 | |||||
| chr3:111651883
|
CA | C | 8 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(5): Show | 76 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2093delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2093 | INFO_REALIGN_3_PRIME | chr3 | 111651883 | ||||
| chr3:111651896
|
A | AAAAAGAA others(14): Show |
1 | a0001c0001t0024 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2093_*2094insAGAA others(17): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2094 | INFO_REALIGN_3_PRIME | chr3 | 111651896 | ||||
| chr3:111651896
|
A | AAAAAGAA others(18): Show |
1 | a0001c0001t0023 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2093_*2094insAGAA others(21): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2094 | INFO_REALIGN_3_PRIME | chr3 | 111651896 | ||||
| chr3:111651896
|
A | AAAAAGAA others(34): Show |
1 | a0001c0001t0022 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2093_*2094insAGAA others(37): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2094 | INFO_REALIGN_3_PRIME | chr3 | 111651896 | ||||
| chr3:111652017
|
A | G | 1 | a0001c0001t0019 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2211A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2211 | chr3 | 111652017 | |||||
| chr3:111652075
|
G | T | 1 | a0001c0001t0018 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2269G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2269 | chr3 | 111652075 | |||||
| chr3:111652093
|
A | C | 1 | a0001c0001t0017 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2287A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2287 | chr3 | 111652093 | |||||
| chr3:111652186
|
C | T | 2 | a0001c0001t0005a0003c0006t0005 | 12 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2380C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2380 | chr3 | 111652186 | |||||
| chr3:111652284
|
C | T | 1 | a0001c0001t0016 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2478C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2478 | chr3 | 111652284 | |||||
| chr3:111652298
|
A | G | 1 | a0001c0001t0025 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2492A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2492 | chr3 | 111652298 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:111542326
|
T | C | 7 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0003g0003others(4): Show | 8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+17T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542326 | ||||||
| chr3:111542357
|
C | T | 1 | a0001c0001t0002g0288 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.61+48C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542357 | ||||||
| chr3:111542395
|
G | GCTGCTGA others(12): Show |
116 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0176others(113): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.61+87_61+105dupCTG others(16): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 111542395 | |||||
| chr3:111542584
|
T | C | 181 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(178): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.61+275T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542584 | ||||||
| chr3:111542670
|
A | G | 6 | a0001c0001t0002g0072a0001c0001t0003g0074a0001c0001t0005g0070others(3): Show | 6 | HG01106.hp1 HG01243.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+361A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542670 | ||||||
| chr3:111542918
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.61+609G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542918 | ||||||
| chr3:111542974
|
C | T | 185 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(182): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.61+665C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542974 | ||||||
| chr3:111542980
|
T | G | 29 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0174others(26): Show | 31 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.61+671T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542980 | ||||||
| chr3:111542983
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(55): Show | 63 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.61+674G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542983 | ||||||
| chr3:111543049
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.61+740G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543049 | ||||||
| chr3:111543364
|
C | T | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+1055C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543364 | ||||||
| chr3:111543365
|
A | G | 185 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(182): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.61+1056A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543365 | ||||||
| chr3:111543456
|
G | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01361.hp1 HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.61+1147G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543456 | ||||||
| chr3:111543532
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.61+1223G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543532 | ||||||
| chr3:111543644
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0007g0130 | 2 | HG01496.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.61+1335G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543644 | ||||||
| chr3:111543746
|
AC | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0005g0039others(1): Show | 4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-1295delC | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 111543746 | |||||
| chr3:111543757
|
T | C | 1 | a0001c0001t0009g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.62-1289T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543757 | ||||||
| chr3:111543815
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(240): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.62-1231T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543815 | ||||||
| chr3:111543907
|
A | G | 185 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0012others(182): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.62-1139A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543907 | ||||||
| chr3:111543910
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.62-1136T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543910 | ||||||
| chr3:111543991
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.62-1055C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543991 | ||||||
| chr3:111544016
|
G | C | 1 | a0001c0001t0004g0181 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.62-1030G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544016 | ||||||
| chr3:111544073
|
G | T | 181 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(178): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.62-973G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544073 | ||||||
| chr3:111544089
|
A | G | 3 | a0001c0001t0005g0062a0001c0001t0021g0061a0001c0005t0006g0060 | 3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.62-957A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544089 | ||||||
| chr3:111544095
|
T | G | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.62-951T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544095 | ||||||
| chr3:111544233
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.62-813C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544233 | ||||||
| chr3:111544434
|
C | T | 3 | a0001c0001t0005g0062a0001c0001t0021g0061a0001c0005t0006g0060 | 3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.62-612C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544434 | ||||||
| chr3:111544557
|
T | A | 181 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(178): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.62-489T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544557 | ||||||
| chr3:111544566
|
C | A | 3 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0020g0042 | 3 | HG02717.hp1 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.62-480C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544566 | ||||||
| chr3:111544578
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0005g0039others(1): Show | 4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-468T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544578 | ||||||
| chr3:111544622
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0126others(2): Show | 8 | HG02027.hp1 HG02074.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-424C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544622 | ||||||
| chr3:111544648
|
TTATATTC others(3): Show |
T | 1 | a0001c0001t0001g0286 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.62-396_62-387delAT others(8): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 111544648 | |||||
| chr3:111544663
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0002g0063 | 2 | HG02886.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.62-383G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544663 | ||||||
| chr3:111544695
|
C | T | 92 | a0001c0001t0001g0010a0001c0001t0001g0176a0001c0001t0001g0177others(89): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.62-351C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544695 | ||||||
| chr3:111544708
|
G | A | 94 | a0001c0001t0001g0010a0001c0001t0001g0176a0001c0001t0001g0177others(91): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.62-338G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544708 | ||||||
| chr3:111544763
|
C | G | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG02132.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.62-283C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544763 | ||||||
| chr3:111544835
|
A | G | 181 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(178): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.62-211A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544835 | ||||||
| chr3:111544869
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.62-177T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544869 | ||||||
| chr3:111544881
|
T | C | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.62-165T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544881 | ||||||
| chr3:111544972
|
G | C | 1 | a0001c0001t0006g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.62-74G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544972 | ||||||
| chr3:111544979
|
G | A | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.62-67G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544979 | ||||||
| chr3:111544995
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.62-51G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544995 | ||||||
| chr3:111545665
|
T | G | 181 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(178): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.418+263T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111545665 | ||||||
| chr3:111545798
|
G | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(30): Show | 35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.418+396G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111545798 | ||||||
| chr3:111545999
|
TA | T | 91 | a0001c0001t0001g0010a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.418+608delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111545999 | |||||
| chr3:111546191
|
A | T | 1 | a0001c0001t0001g0010 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.418+789A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546191 | ||||||
| chr3:111546338
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.418+936T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546338 | ||||||
| chr3:111546419
|
C | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.418+1017C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546419 | ||||||
| chr3:111546419
|
C | T | 159 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(156): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.418+1017C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546419 | ||||||
| chr3:111546579
|
T | C | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+1177T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546579 | ||||||
| chr3:111546698
|
G | A | 2 | a0001c0001t0002g0041a0001c0001t0020g0042 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.418+1296G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546698 | ||||||
| chr3:111546706
|
C | T | 15 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0056others(12): Show | 15 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.418+1304C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546706 | ||||||
| chr3:111546919
|
T | TAC | 18 | a0001c0001t0001g0076a0001c0001t0001g0134a0001c0001t0001g0138others(15): Show | 18 | HG00621.hp1 HG00738.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.418+1544_418+1545d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACAC | 5 | a0001c0001t0001g0043a0001c0001t0003g0066a0001c0001t0005g0039others(2): Show | 5 | HG02055.hp1 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+1542_418+1545d others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACACAC | 4 | a0001c0001t0003g0074a0001c0001t0006g0073a0001c0001t0023g0057others(1): Show | 4 | HG02055.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+1540_418+1545d others(8): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACACACA others(1): Show |
16 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0052others(13): Show | 16 | HG01192.hp2 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.418+1538_418+1545d others(10): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACACACA others(3): Show |
5 | a0001c0001t0001g0033a0001c0001t0003g0048a0001c0001t0006g0069others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+1536_418+1545d others(12): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACACACA others(5): Show |
24 | a0001c0001t0001g0012a0001c0001t0001g0174a0001c0001t0002g0014others(21): Show | 26 | HG00408.hp2 HG01952.hp2 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.418+1534_418+1545d others(14): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACACACA others(7): Show |
9 | a0001c0001t0001g0010a0001c0001t0002g0072a0001c0001t0005g0047others(6): Show | 10 | HG00544.hp1 HG00544.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.418+1532_418+1545d others(16): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACACACA others(9): Show |
7 | a0001c0001t0001g0179a0001c0001t0001g0280a0001c0001t0001g0281others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.418+1530_418+1545d others(18): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACACACA others(11): Show |
21 | a0001c0001t0001g0178a0001c0001t0001g0206a0001c0001t0001g0207others(18): Show | 22 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.418+1528_418+1545d others(20): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACACACA others(13): Show |
16 | a0001c0001t0001g0205a0001c0001t0001g0251a0001c0001t0001g0252others(13): Show | 16 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(13): Show |
intron_variant | MODIFIER | c.418+1526_418+1545d others(22): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACACACA others(15): Show |
34 | a0001c0001t0001g0045a0001c0001t0001g0176a0001c0001t0001g0177others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.418+1524_418+1545d others(24): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACACACA others(17): Show |
8 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(5): Show | 9 | HG02027.hp2 HG02074.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.418+1522_418+1545d others(26): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACACACA others(19): Show |
3 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0003g0213 | 3 | HG00438.hp2 HG01256.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.418+1520_418+1545d others(28): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACACACA others(21): Show |
1 | a0001c0001t0003g0211 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.418+1518_418+1545d others(30): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TACACACA others(23): Show |
2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG01074.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.418+1545_418+1546i others(32): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111546919
|
T | TTACACAC others(12): Show |
1 | a0001c0001t0001g0285 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.418+1517_418+1518i others(21): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546919 | ||||||
| chr3:111546919
|
TACAC | T | 3 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0020g0042 | 3 | HG02717.hp1 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.418+1542_418+1545d others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | |||||
| chr3:111547114
|
C | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(59): Show | 68 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.418+1712C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547114 | ||||||
| chr3:111547139
|
T | C | 1 | a0001c0001t0008g0264 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.418+1737T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547139 | ||||||
| chr3:111547309
|
T | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0251 | 2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.418+1907T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547309 | ||||||
| chr3:111547416
|
GT | G | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+2022delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111547416 | |||||
| chr3:111547465
|
C | T | 2 | a0001c0001t0001g0033a0007c0008t0001g0034 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.418+2063C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547465 | ||||||
| chr3:111547518
|
T | C | 3 | a0001c0001t0009g0049a0001c0001t0009g0050a0001c0001t0009g0051 | 3 | HG01192.hp2 HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.418+2116T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547518 | ||||||
| chr3:111547701
|
T | C | 11 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0002g0053others(8): Show | 11 | HG01192.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.418+2299T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547701 | ||||||
| chr3:111547715
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0005g0039others(1): Show | 4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+2313G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547715 | ||||||
| chr3:111547729
|
C | T | 21 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0056others(18): Show | 21 | HG01106.hp1 HG01192.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.418+2327C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547729 | ||||||
| chr3:111547763
|
G | A | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+2361G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547763 | ||||||
| chr3:111547966
|
T | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(30): Show | 35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.418+2564T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547966 | ||||||
| chr3:111548368
|
T | A | 1 | a0001c0001t0001g0077 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.418+2966T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548368 | ||||||
| chr3:111548640
|
T | C | 1 | a0001c0001t0006g0185 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.418+3238T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548640 | ||||||
| chr3:111548656
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.418+3254G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548656 | ||||||
| chr3:111548717
|
C | T | 180 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(177): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.418+3315C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548717 | ||||||
| chr3:111548848
|
C | T | 3 | a0001c0001t0001g0286a0001c0001t0002g0249a0001c0001t0002g0250 | 3 | HG00099.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.418+3446C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548848 | ||||||
| chr3:111548894
|
G | C | 1 | a0001c0001t0003g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.418+3492G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548894 | ||||||
| chr3:111548898
|
T | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(30): Show | 35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.418+3496T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548898 | ||||||
| chr3:111548934
|
G | A | 3 | a0001c0001t0005g0062a0001c0001t0021g0061a0001c0005t0006g0060 | 3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.418+3532G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548934 | ||||||
| chr3:111548961
|
G | A | 18 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0056others(15): Show | 18 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.418+3559G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548961 | ||||||
| chr3:111548983
|
G | T | 1 | a0001c0001t0003g0016 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.418+3581G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548983 | ||||||
| chr3:111549121
|
C | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+3719C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111549121 | ||||||
| chr3:111549364
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.418+3962C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111549364 | ||||||
| chr3:111549499
|
C | G | 1 | a0001c0001t0022g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.418+4097C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111549499 | ||||||
| chr3:111549500
|
A | G | 93 | a0001c0001t0001g0010a0001c0001t0001g0176a0001c0001t0001g0177others(90): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.418+4098A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111549500 | ||||||
| chr3:111549507
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.418+4105G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111549507 | ||||||
| chr3:111550039
|
C | T | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+4637C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550039 | ||||||
| chr3:111550389
|
G | A | 93 | a0001c0001t0001g0010a0001c0001t0001g0176a0001c0001t0001g0177others(90): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.418+4987G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550389 | ||||||
| chr3:111550483
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.418+5081G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550483 | ||||||
| chr3:111550533
|
G | A | 1 | a0001c0001t0008g0265 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.418+5131G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550533 | ||||||
| chr3:111550702
|
C | G | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+5300C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550702 | ||||||
| chr3:111550872
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.418+5470G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550872 | ||||||
| chr3:111550942
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.418+5540G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550942 | ||||||
| chr3:111551173
|
A | G | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+5771A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551173 | ||||||
| chr3:111551181
|
A | G | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+5779A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551181 | ||||||
| chr3:111551297
|
G | T | 3 | a0001c0001t0002g0072a0001c0001t0005g0070a0001c0001t0005g0071 | 3 | HG01106.hp1 HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.418+5895G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551297 | ||||||
| chr3:111551400
|
A | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+5998A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551400 | ||||||
| chr3:111551410
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.418+6008A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551410 | ||||||
| chr3:111551419
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0005g0039others(1): Show | 4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+6017C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551419 | ||||||
| chr3:111551483
|
C | A | 1 | a0006c0010t0007g0222 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.418+6081C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551483 | ||||||
| chr3:111551879
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.418+6477C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551879 | ||||||
| chr3:111552145
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.418+6743T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552145 | ||||||
| chr3:111552164
|
G | C | 1 | a0006c0010t0007g0222 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.418+6762G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552164 | ||||||
| chr3:111552249
|
T | C | 2 | a0001c0001t0010g0019a0002c0002t0002g0017 | 2 | HG00544.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.418+6847T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552249 | ||||||
| chr3:111552274
|
G | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+6872G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552274 | ||||||
| chr3:111552281
|
T | A | 2 | a0001c0001t0002g0041a0001c0001t0020g0042 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.418+6879T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552281 | ||||||
| chr3:111552467
|
C | T | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(259): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.418+7065C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552467 | ||||||
| chr3:111552555
|
G | C | 2 | a0001c0001t0005g0070a0001c0001t0005g0071 | 2 | HG01106.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.418+7153G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552555 | ||||||
| chr3:111552604
|
T | TAAAAAGC others(323): Show |
2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.418+7218_418+7219i others(332): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111552604 | |||||
| chr3:111552604
|
T | TAAAAAGC others(324): Show |
2 | a0001c0001t0005g0039a0001c0011t0026g0036 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.418+7218_418+7219i others(333): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111552604 | |||||
| chr3:111552637
|
G | A | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+7235G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552637 | ||||||
| chr3:111552774
|
T | G | 1 | a0001c0003t0001g0020 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.418+7372T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552774 | ||||||
| chr3:111553072
|
A | T | 1 | a0001c0001t0005g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.418+7670A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553072 | ||||||
| chr3:111553083
|
TA | T | 7 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0123others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.418+7689delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111553083 | |||||
| chr3:111553158
|
G | GATA | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.418+7758_418+7759i others(5): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111553158 | |||||
| chr3:111553171
|
G | GT | 10 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0003g0003others(7): Show | 11 | HG02257.hp1 HG02559.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.418+7780dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111553171 | |||||
| chr3:111553171
|
GT | G | 23 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0056others(20): Show | 23 | HG01106.hp1 HG01192.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.418+7780delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111553171 | |||||
| chr3:111553207
|
T | C | 1 | a0001c0003t0001g0020 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.418+7805T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553207 | ||||||
| chr3:111553239
|
T | C | 3 | a0001c0001t0002g0072a0001c0001t0005g0070a0001c0001t0005g0071 | 3 | HG01106.hp1 HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.418+7837T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553239 | ||||||
| chr3:111553253
|
T | C | 4 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0008g0143others(1): Show | 4 | HG00735.hp1 HG01361.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+7851T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553253 | ||||||
| chr3:111553254
|
A | G | 4 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(1): Show | 4 | HG02055.hp1 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+7852A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553254 | ||||||
| chr3:111553413
|
A | C | 182 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(179): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.418+8011A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553413 | ||||||
| chr3:111553434
|
CT | C | 177 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(174): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.418+8047delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111553434 | |||||
| chr3:111553436
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.418+8034T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553436 | ||||||
| chr3:111553437
|
T | G | 17 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0002g0053others(14): Show | 17 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.418+8035T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553437 | ||||||
| chr3:111553946
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0007g0187 | 2 | HG00639.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.418+8544G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553946 | ||||||
| chr3:111554024
|
G | T | 19 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0168others(16): Show | 19 | HG02145.hp1 HG02486.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.418+8622G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554024 | ||||||
| chr3:111554091
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.418+8689C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554091 | ||||||
| chr3:111554211
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.418+8809T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554211 | ||||||
| chr3:111554300
|
C | G | 1 | a0001c0001t0014g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418+8898C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554300 | ||||||
| chr3:111554329
|
A | G | 2 | a0001c0001t0002g0041a0001c0001t0020g0042 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.418+8927A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554329 | ||||||
| chr3:111554403
|
T | A | 2 | a0001c0001t0002g0147a0001c0001t0003g0148 | 2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.418+9001T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554403 | ||||||
| chr3:111554456
|
T | G | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | NA18969.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.418+9054T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554456 | ||||||
| chr3:111554479
|
G | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+9077G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554479 | ||||||
| chr3:111554629
|
A | C | 7 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0003g0003others(4): Show | 8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.418+9227A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554629 | ||||||
| chr3:111554659
|
G | T | 2 | a0002c0002t0001g0030a0002c0002t0001g0031 | 2 | NA18959.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.418+9257G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554659 | ||||||
| chr3:111554685
|
T | G | 182 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(179): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.418+9283T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554685 | ||||||
| chr3:111554753
|
T | C | 93 | a0001c0001t0001g0010a0001c0001t0001g0176a0001c0001t0001g0177others(90): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.418+9351T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554753 | ||||||
| chr3:111554992
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.418+9590A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554992 | ||||||
| chr3:111555081
|
G | A | 29 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0174others(26): Show | 31 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.418+9679G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555081 | ||||||
| chr3:111555118
|
T | C | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0002g0078others(8): Show | 11 | HG00609.hp2 NA18945.hp1 NA18969.hp2 others(8): Show |
intron_variant | MODIFIER | c.418+9716T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555118 | ||||||
| chr3:111555220
|
A | G | 41 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(38): Show | 43 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.418+9818A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555220 | ||||||
| chr3:111555303
|
C | T | 21 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0056others(18): Show | 21 | HG01106.hp1 HG01192.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.418+9901C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555303 | ||||||
| chr3:111555385
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.418+9983A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555385 | ||||||
| chr3:111555418
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.418+10016C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555418 | ||||||
| chr3:111555442
|
A | G | 1 | a0002c0002t0001g0031 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.418+10040A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555442 | ||||||
| chr3:111555681
|
G | T | 1 | a0001c0001t0001g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.418+10279G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555681 | ||||||
| chr3:111555758
|
G | T | 93 | a0001c0001t0001g0010a0001c0001t0001g0176a0001c0001t0001g0177others(90): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.418+10356G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555758 | ||||||
| chr3:111556013
|
G | A | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+10611G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556013 | ||||||
| chr3:111556075
|
C | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+10673C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556075 | ||||||
| chr3:111556206
|
CT | C | 27 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0180others(24): Show | 27 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.418+10814delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111556206 | |||||
| chr3:111556216
|
T | A | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+10814T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556216 | ||||||
| chr3:111556225
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.418+10823T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556225 | ||||||
| chr3:111556247
|
A | G | 5 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.418+10845A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556247 | ||||||
| chr3:111556296
|
C | T | 23 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(20): Show | 23 | HG00621.hp2 HG00639.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.418+10894C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556296 | ||||||
| chr3:111556301
|
C | G | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+10899C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556301 | ||||||
| chr3:111556431
|
A | T | 1 | a0001c0012t0006g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.418+11029A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556431 | ||||||
| chr3:111556451
|
G | C | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+11049G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556451 | ||||||
| chr3:111556473
|
C | T | 33 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(30): Show | 35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.419-11050C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556473 | ||||||
| chr3:111556490
|
A | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(270): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.419-11033A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556490 | ||||||
| chr3:111556560
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.419-10963T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556560 | ||||||
| chr3:111556565
|
C | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-10958C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556565 | ||||||
| chr3:111556577
|
T | G | 11 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0197others(8): Show | 11 | HG01081.hp1 HG02572.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.419-10946T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556577 | ||||||
| chr3:111556646
|
A | G | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-10877A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556646 | ||||||
| chr3:111556698
|
A | G | 1 | a0001c0001t0020g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.419-10825A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556698 | ||||||
| chr3:111556737
|
C | G | 24 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(21): Show | 24 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.419-10786C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556737 | ||||||
| chr3:111556746
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.419-10777T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556746 | ||||||
| chr3:111556783
|
G | C | 6 | a0001c0001t0001g0134a0001c0001t0002g0005a0001c0001t0002g0132others(3): Show | 6 | HG02735.hp2 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-10740G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556783 | ||||||
| chr3:111556812
|
G | C | 2 | a0001c0001t0023g0057a0001c0001t0024g0058 | 2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.419-10711G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556812 | ||||||
| chr3:111556892
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(240): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.419-10631T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556892 | ||||||
| chr3:111556951
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.419-10572G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556951 | ||||||
| chr3:111556989
|
A | T | 182 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(179): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.419-10534A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556989 | ||||||
| chr3:111557031
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(76): Show | 85 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.419-10492C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557031 | ||||||
| chr3:111557034
|
A | C | 19 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0056others(16): Show | 19 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.419-10489A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557034 | ||||||
| chr3:111557160
|
G | C | 1 | a0001c0001t0004g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.419-10363G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557160 | ||||||
| chr3:111557188
|
G | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-10335G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557188 | ||||||
| chr3:111557192
|
A | G | 1 | a0001c0003t0001g0020 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.419-10331A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557192 | ||||||
| chr3:111557215
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.419-10308T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557215 | ||||||
| chr3:111557222
|
C | T | 65 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(62): Show | 67 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.419-10301C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557222 | ||||||
| chr3:111557225
|
C | G | 2 | a0001c0001t0001g0261a0001c0001t0002g0262 | 2 | HG00438.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.419-10298C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557225 | ||||||
| chr3:111557233
|
G | T | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0261others(3): Show | 6 | HG00438.hp1 HG02895.hp2 NA19030.hp2 others(3): Show |
intron_variant | MODIFIER | c.419-10290G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557233 | ||||||
| chr3:111557262
|
A | G | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-10261A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557262 | ||||||
| chr3:111557397
|
G | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(30): Show | 35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.419-10126G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557397 | ||||||
| chr3:111557429
|
G | A | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-10094G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557429 | ||||||
| chr3:111557447
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.419-10076A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557447 | ||||||
| chr3:111557473
|
C | G | 2 | a0001c0001t0001g0045a0001c0001t0010g0046 | 2 | HG02258.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.419-10050C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557473 | ||||||
| chr3:111557487
|
C | G | 1 | a0002c0002t0001g0029 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.419-10036C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557487 | ||||||
| chr3:111557518
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.419-10005G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557518 | ||||||
| chr3:111557523
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.419-10000C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557523 | ||||||
| chr3:111557528
|
T | A | 1 | a0001c0001t0005g0188 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.419-9995T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557528 | ||||||
| chr3:111557599
|
G | T | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-9924G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557599 | ||||||
| chr3:111557625
|
G | A | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-9898G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557625 | ||||||
| chr3:111557666
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.419-9857T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557666 | ||||||
| chr3:111557669
|
G | C | 2 | a0001c0001t0001g0129a0001c0001t0007g0130 | 2 | HG01496.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.419-9854G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557669 | ||||||
| chr3:111557681
|
C | T | 1 | a0001c0001t0002g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.419-9842C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557681 | ||||||
| chr3:111557682
|
G | A | 3 | a0001c0001t0005g0062a0001c0001t0021g0061a0001c0005t0006g0060 | 3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-9841G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557682 | ||||||
| chr3:111557686
|
C | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-9837C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557686 | ||||||
| chr3:111557751
|
T | A | 1 | a0003c0006t0003g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.419-9772T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557751 | ||||||
| chr3:111557922
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0010g0046 | 2 | HG02258.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.419-9601A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557922 | ||||||
| chr3:111557936
|
G | T | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-9587G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557936 | ||||||
| chr3:111558106
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-9417G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558106 | ||||||
| chr3:111558132
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.419-9391T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558132 | ||||||
| chr3:111558170
|
C | T | 3 | a0001c0001t0005g0062a0001c0001t0021g0061a0001c0005t0006g0060 | 3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-9353C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558170 | ||||||
| chr3:111558314
|
G | A | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-9209G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558314 | ||||||
| chr3:111558376
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.419-9147G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558376 | ||||||
| chr3:111558390
|
G | T | 25 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0180others(22): Show | 25 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.419-9133G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558390 | ||||||
| chr3:111558417
|
G | T | 93 | a0001c0001t0001g0010a0001c0001t0001g0176a0001c0001t0001g0177others(90): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.419-9106G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558417 | ||||||
| chr3:111558441
|
T | C | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-9082T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558441 | ||||||
| chr3:111558443
|
T | C | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-9080T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558443 | ||||||
| chr3:111558519
|
G | A | 11 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0002g0053others(8): Show | 11 | HG01192.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.419-9004G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558519 | ||||||
| chr3:111558656
|
G | T | 1 | a0001c0001t0001g0124 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.419-8867G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558656 | ||||||
| chr3:111558691
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(58): Show | 67 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.419-8832G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558691 | ||||||
| chr3:111558705
|
A | G | 5 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0280others(2): Show | 5 | HG01952.hp1 HG01978.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-8818A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558705 | ||||||
| chr3:111558737
|
G | T | 1 | a0001c0001t0007g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.419-8786G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558737 | ||||||
| chr3:111558816
|
G | A | 1 | a0001c0001t0022g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.419-8707G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558816 | ||||||
| chr3:111558873
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0005g0039others(1): Show | 4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-8650C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558873 | ||||||
| chr3:111558910
|
G | T | 1 | a0001c0001t0001g0245 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.419-8613G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558910 | ||||||
| chr3:111558971
|
C | A | 1 | a0001c0001t0001g0266 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.419-8552C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558971 | ||||||
| chr3:111559045
|
G | C | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.419-8478G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559045 | ||||||
| chr3:111559271
|
G | C | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.419-8252G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559271 | ||||||
| chr3:111559383
|
A | G | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-8140A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559383 | ||||||
| chr3:111559458
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.419-8065G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559458 | ||||||
| chr3:111559553
|
T | C | 1 | a0001c0001t0007g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.419-7970T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559553 | ||||||
| chr3:111559568
|
A | T | 9 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0199others(6): Show | 9 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.419-7955A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559568 | ||||||
| chr3:111559618
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.419-7905T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559618 | ||||||
| chr3:111559628
|
C | G | 1 | a0001c0001t0001g0122 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.419-7895C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559628 | ||||||
| chr3:111559638
|
A | C | 13 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0161others(10): Show | 13 | HG01071.hp2 HG01099.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.419-7885A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559638 | ||||||
| chr3:111559725
|
T | C | 7 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0003g0003others(4): Show | 8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-7798T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559725 | ||||||
| chr3:111559728
|
G | T | 183 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(180): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.419-7795G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559728 | ||||||
| chr3:111559780
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0003g0003others(4): Show | 8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-7743G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559780 | ||||||
| chr3:111559833
|
G | T | 7 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0003g0003others(4): Show | 8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-7690G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559833 | ||||||
| chr3:111559929
|
T | C | 7 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0003g0003others(4): Show | 8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-7594T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559929 | ||||||
| chr3:111559982
|
T | G | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-7541T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559982 | ||||||
| chr3:111560082
|
T | C | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-7441T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560082 | ||||||
| chr3:111560109
|
C | T | 93 | a0001c0001t0001g0010a0001c0001t0001g0176a0001c0001t0001g0177others(90): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.419-7414C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560109 | ||||||
| chr3:111560192
|
A | C | 5 | a0001c0001t0001g0224a0001c0001t0001g0241a0001c0001t0001g0242others(2): Show | 5 | NA18950.hp1 NA18952.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-7331A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560192 | ||||||
| chr3:111560203
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.419-7320T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560203 | ||||||
| chr3:111560222
|
G | T | 3 | a0001c0001t0002g0041a0001c0001t0020g0042a0006c0010t0007g0222 | 3 | HG01255.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.419-7301G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560222 | ||||||
| chr3:111560448
|
A | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-7075A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560448 | ||||||
| chr3:111560578
|
A | G | 23 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(20): Show | 23 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.419-6945A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560578 | ||||||
| chr3:111560578
|
A | T | 1 | a0001c0003t0001g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.419-6945A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560578 | ||||||
| chr3:111560604
|
G | A | 2 | a0001c0001t0003g0211a0001c0001t0003g0213 | 2 | HG00438.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.419-6919G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560604 | ||||||
| chr3:111560681
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.419-6842T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560681 | ||||||
| chr3:111560701
|
C | A | 1 | a0001c0001t0001g0225 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.419-6822C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560701 | ||||||
| chr3:111560741
|
T | G | 1 | a0001c0001t0001g0226 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.419-6782T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560741 | ||||||
| chr3:111560747
|
C | T | 2 | a0001c0001t0001g0120a0001c0015t0001g0119 | 2 | NA18939.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.419-6776C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560747 | ||||||
| chr3:111560942
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0022g0044 | 3 | HG02486.hp2 HG02683.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.419-6581G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560942 | ||||||
| chr3:111560997
|
A | G | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-6526A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560997 | ||||||
| chr3:111561001
|
T | C | 56 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(53): Show | 58 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.419-6522T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561001 | ||||||
| chr3:111561035
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.419-6488C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561035 | ||||||
| chr3:111561045
|
G | A | 9 | a0001c0001t0002g0147a0001c0001t0003g0148a0001c0001t0004g0144others(6): Show | 9 | HG00735.hp1 HG01361.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.419-6478G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561045 | ||||||
| chr3:111561046
|
G | GT | 21 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0056others(18): Show | 21 | HG01106.hp1 HG01192.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.419-6473dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111561046 | |||||
| chr3:111561060
|
C | G | 14 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0002g0005others(11): Show | 14 | HG02523.hp2 HG02735.hp2 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.419-6463C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561060 | ||||||
| chr3:111561079
|
T | A | 1 | a0001c0001t0001g0205 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.419-6444T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561079 | ||||||
| chr3:111561081
|
T | C | 21 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0056others(18): Show | 21 | HG01106.hp1 HG01192.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.419-6442T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561081 | ||||||
| chr3:111561082
|
G | A | 2 | a0001c0001t0002g0041a0001c0001t0020g0042 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.419-6441G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561082 | ||||||
| chr3:111561114
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.419-6409A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561114 | ||||||
| chr3:111561135
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.419-6388T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561135 | ||||||
| chr3:111561164
|
G | A | 2 | a0001c0001t0002g0249a0001c0001t0002g0250 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.419-6359G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561164 | ||||||
| chr3:111561189
|
G | A | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-6334G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561189 | ||||||
| chr3:111561195
|
T | G | 3 | a0001c0001t0005g0062a0001c0001t0021g0061a0001c0005t0006g0060 | 3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-6328T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561195 | ||||||
| chr3:111561196
|
T | C | 3 | a0001c0001t0005g0062a0001c0001t0021g0061a0001c0005t0006g0060 | 3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-6327T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561196 | ||||||
| chr3:111561241
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0003g0003others(4): Show | 8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-6282G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561241 | ||||||
| chr3:111561259
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0252 | 2 | HG01167.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.419-6264T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561259 | ||||||
| chr3:111561282
|
G | A | 1 | a0001c0001t0008g0143 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.419-6241G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561282 | ||||||
| chr3:111561315
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.419-6208C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561315 | ||||||
| chr3:111561347
|
C | T | 33 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(30): Show | 35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.419-6176C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561347 | ||||||
| chr3:111561350
|
T | C | 1 | a0002c0002t0001g0030 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.419-6173T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561350 | ||||||
| chr3:111561352
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-6171G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561352 | ||||||
| chr3:111561374
|
C | A | 2 | a0001c0001t0002g0035a0001c0001t0022g0044 | 2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.419-6149C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561374 | ||||||
| chr3:111561386
|
C | T | 1 | a0002c0002t0001g0029 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.419-6137C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561386 | ||||||
| chr3:111561389
|
T | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(59): Show | 68 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.419-6134T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561389 | ||||||
| chr3:111561462
|
C | T | 1 | a0001c0003t0001g0020 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.419-6061C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561462 | ||||||
| chr3:111561466
|
C | T | 3 | a0001c0001t0005g0062a0001c0001t0021g0061a0001c0005t0006g0060 | 3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-6057C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561466 | ||||||
| chr3:111561468
|
T | G | 100 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0092others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.419-6055T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561468 | ||||||
| chr3:111561480
|
A | G | 1 | a0007c0008t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.419-6043A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561480 | ||||||
| chr3:111561495
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.419-6028C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561495 | ||||||
| chr3:111561496
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.419-6027G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561496 | ||||||
| chr3:111561529
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.419-5994G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561529 | ||||||
| chr3:111561563
|
G | C | 11 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0206others(8): Show | 11 | HG00099.hp2 HG01952.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.419-5960G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561563 | ||||||
| chr3:111561564
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0005g0039others(1): Show | 4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-5959G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561564 | ||||||
| chr3:111561575
|
T | G | 1 | a0001c0001t0002g0078 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.419-5948T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561575 | ||||||
| chr3:111561581
|
T | C | 2 | a0001c0001t0001g0286a0001c0001t0005g0188 | 2 | HG00099.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.419-5942T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561581 | ||||||
| chr3:111561623
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-5900A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561623 | ||||||
| chr3:111561648
|
A | C | 4 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0020g0042others(1): Show | 4 | HG02717.hp1 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-5875A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561648 | ||||||
| chr3:111561664
|
TTGTC | T | 4 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(1): Show | 4 | HG02055.hp1 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-5855_419-5852d others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111561664 | |||||
| chr3:111561720
|
G | A | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-5803G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561720 | ||||||
| chr3:111561743
|
C | G | 33 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(30): Show | 35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.419-5780C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561743 | ||||||
| chr3:111561744
|
G | C | 1 | a0001c0001t0001g0093 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.419-5779G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561744 | ||||||
| chr3:111561744
|
G | T | 1 | a0001c0001t0013g0067 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.419-5779G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561744 | ||||||
| chr3:111561752
|
C | T | 33 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(30): Show | 35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.419-5771C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561752 | ||||||
| chr3:111561753
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.419-5770G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561753 | ||||||
| chr3:111561761
|
T | C | 2 | a0002c0002t0001g0030a0002c0002t0001g0031 | 2 | NA18959.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.419-5762T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561761 | ||||||
| chr3:111561772
|
G | T | 1 | a0001c0001t0022g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.419-5751G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561772 | ||||||
| chr3:111561862
|
T | C | 32 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0056others(29): Show | 32 | HG01071.hp2 HG01099.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.419-5661T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561862 | ||||||
| chr3:111561865
|
C | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-5658C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561865 | ||||||
| chr3:111561871
|
C | T | 2 | a0001c0001t0002g0041a0001c0001t0020g0042 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.419-5652C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561871 | ||||||
| chr3:111561930
|
G | A | 4 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(1): Show | 4 | HG02055.hp1 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-5593G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561930 | ||||||
| chr3:111561951
|
G | A | 1 | a0001c0001t0002g0227 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.419-5572G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561951 | ||||||
| chr3:111561964
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-5559C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561964 | ||||||
| chr3:111561984
|
G | A | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-5539G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561984 | ||||||
| chr3:111562003
|
C | T | 1 | a0001c0001t0003g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.419-5520C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562003 | ||||||
| chr3:111562080
|
G | A | 2 | a0001c0001t0001g0033a0007c0008t0001g0034 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.419-5443G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562080 | ||||||
| chr3:111562234
|
C | A | 2 | a0001c0001t0002g0041a0001c0001t0020g0042 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.419-5289C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562234 | ||||||
| chr3:111562302
|
C | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-5221C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562302 | ||||||
| chr3:111562329
|
C | T | 19 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0195others(16): Show | 19 | HG00738.hp1 HG01074.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.419-5194C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562329 | ||||||
| chr3:111562535
|
C | CA | 191 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(188): Show | 196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.419-4988_419-4987i others(3): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562535 | ||||||
| chr3:111562600
|
C | A | 1 | a0001c0001t0001g0252 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.419-4923C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562600 | ||||||
| chr3:111562678
|
C | A | 1 | a0001c0001t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-4845C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562678 | ||||||
| chr3:111562711
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.419-4812A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562711 | ||||||
| chr3:111562759
|
C | G | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-4764C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562759 | ||||||
| chr3:111562842
|
A | G | 1 | a0001c0001t0002g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.419-4681A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562842 | ||||||
| chr3:111563017
|
C | T | 95 | a0001c0001t0001g0010a0001c0001t0001g0174a0001c0001t0001g0176others(92): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.419-4506C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563017 | ||||||
| chr3:111563039
|
G | T | 11 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0197others(8): Show | 11 | HG01081.hp1 HG02572.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.419-4484G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563039 | ||||||
| chr3:111563175
|
C | T | 1 | a0001c0001t0004g0164 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.419-4348C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563175 | ||||||
| chr3:111563184
|
A | C | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-4339A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563184 | ||||||
| chr3:111563187
|
C | A | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.419-4336C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563187 | ||||||
| chr3:111563212
|
A | C | 2 | a0001c0001t0001g0186a0001c0001t0007g0187 | 2 | HG00639.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.419-4311A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563212 | ||||||
| chr3:111563512
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.419-4011C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563512 | ||||||
| chr3:111563572
|
C | T | 1 | a0001c0001t0005g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.419-3951C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563572 | ||||||
| chr3:111563582
|
ATTG | A | 4 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(1): Show | 4 | HG02055.hp1 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-3932_419-3930d others(5): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111563582 | |||||
| chr3:111563717
|
A | G | 39 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(36): Show | 41 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.419-3806A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563717 | ||||||
| chr3:111563841
|
T | C | 1 | a0002c0002t0002g0175 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.419-3682T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563841 | ||||||
| chr3:111563872
|
G | A | 1 | a0001c0001t0002g0121 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.419-3651G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563872 | ||||||
| chr3:111563896
|
T | C | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-3627T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563896 | ||||||
| chr3:111563982
|
C | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-3541C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563982 | ||||||
| chr3:111564023
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0005g0039others(1): Show | 4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-3500G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564023 | ||||||
| chr3:111564150
|
C | G | 2 | a0001c0001t0002g0035a0001c0001t0022g0044 | 2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.419-3373C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564150 | ||||||
| chr3:111564150
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.419-3373C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564150 | ||||||
| chr3:111564208
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.419-3315T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564208 | ||||||
| chr3:111564226
|
T | C | 2 | a0001c0005t0006g0150a0001c0005t0006g0151 | 2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.419-3297T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564226 | ||||||
| chr3:111564284
|
C | A | 2 | a0001c0001t0001g0177a0001c0001t0004g0153 | 2 | HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.419-3239C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564284 | ||||||
| chr3:111564468
|
TA | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-3050delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111564468 | |||||
| chr3:111564503
|
C | T | 21 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(18): Show | 21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-3020C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564503 | ||||||
| chr3:111564535
|
A | G | 1 | a0001c0001t0010g0019 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.419-2988A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564535 | ||||||
| chr3:111564594
|
G | C | 19 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0195others(16): Show | 19 | HG00738.hp1 HG01074.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.419-2929G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564594 | ||||||
| chr3:111564682
|
T | A | 7 | a0001c0001t0001g0271a0001c0001t0001g0287a0001c0001t0008g0009others(4): Show | 8 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-2841T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564682 | ||||||
| chr3:111564708
|
G | A | 7 | a0001c0001t0001g0271a0001c0001t0001g0287a0001c0001t0008g0009others(4): Show | 8 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-2815G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564708 | ||||||
| chr3:111564881
|
G | A | 1 | a0007c0008t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.419-2642G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564881 | ||||||
| chr3:111565077
|
G | A | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG00735.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.419-2446G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565077 | ||||||
| chr3:111565264
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.419-2259C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565264 | ||||||
| chr3:111565565
|
G | A | 7 | a0001c0001t0001g0180a0001c0001t0001g0199a0001c0001t0001g0202others(4): Show | 7 | HG00738.hp1 HG01074.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.419-1958G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565565 | ||||||
| chr3:111565565
|
G | T | 2 | a0001c0001t0002g0041a0001c0001t0020g0042 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.419-1958G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565565 | ||||||
| chr3:111565614
|
G | T | 22 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0028others(19): Show | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-1909G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565614 | ||||||
| chr3:111565648
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-1875T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565648 | ||||||
| chr3:111565714
|
T | G | 22 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0028others(19): Show | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-1809T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565714 | ||||||
| chr3:111565898
|
T | C | 22 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0028others(19): Show | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-1625T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565898 | ||||||
| chr3:111565999
|
A | G | 2 | a0001c0003t0001g0020a0001c0003t0001g0146 | 2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.419-1524A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565999 | ||||||
| chr3:111566017
|
T | A | 91 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0174others(88): Show | 93 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.419-1506T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566017 | ||||||
| chr3:111566039
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-1484T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566039 | ||||||
| chr3:111566167
|
C | T | 22 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0028others(19): Show | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-1356C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566167 | ||||||
| chr3:111566168
|
G | A | 3 | a0001c0001t0001g0094a0001c0011t0026g0036a0001c0014t0001g0095 | 3 | HG01255.hp1 HG01358.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.419-1355G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566168 | ||||||
| chr3:111566204
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.419-1319T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566204 | ||||||
| chr3:111566247
|
T | G | 10 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0161others(7): Show | 10 | HG01071.hp2 HG01099.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.419-1276T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566247 | ||||||
| chr3:111566287
|
G | A | 22 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0028others(19): Show | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-1236G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566287 | ||||||
| chr3:111566672
|
A | T | 22 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0028others(19): Show | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-851A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566672 | ||||||
| chr3:111566970
|
T | A | 22 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0028others(19): Show | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-553T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566970 | ||||||
| chr3:111566976
|
C | A | 7 | a0001c0001t0001g0271a0001c0001t0001g0287a0001c0001t0008g0009others(4): Show | 8 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-547C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566976 | ||||||
| chr3:111567029
|
C | T | 53 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0155others(50): Show | 53 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.419-494C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111567029 | ||||||
| chr3:111567030
|
G | T | 1 | a0001c0001t0022g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.419-493G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111567030 | ||||||
| chr3:111567272
|
C | G | 184 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(181): Show | 188 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.419-251C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111567272 | ||||||
| chr3:111567912
|
G | A | 22 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0028others(19): Show | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+265G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111567912 | ||||||
| chr3:111568042
|
T | G | 21 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0028others(18): Show | 22 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.543+395T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111568042 | ||||||
| chr3:111568378
|
C | T | 22 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0028others(19): Show | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+731C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111568378 | ||||||
| chr3:111568401
|
A | C | 22 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0028others(19): Show | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+754A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111568401 | ||||||
| chr3:111568715
|
G | T | 2 | a0001c0001t0002g0249a0001c0001t0002g0250 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.543+1068G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111568715 | ||||||
| chr3:111568724
|
C | T | 5 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG02572.hp2 HG02895.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+1077C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111568724 | ||||||
| chr3:111568733
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.543+1086C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111568733 | ||||||
| chr3:111569022
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.543+1375T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569022 | ||||||
| chr3:111569215
|
T | C | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG00735.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.543+1568T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569215 | ||||||
| chr3:111569352
|
C | T | 22 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0028others(19): Show | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+1705C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569352 | ||||||
| chr3:111569600
|
T | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(285): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.543+1953T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569600 | ||||||
| chr3:111569607
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.543+1960C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569607 | ||||||
| chr3:111569666
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.543+2019C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569666 | ||||||
| chr3:111569692
|
C | T | 50 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0117others(47): Show | 50 | HG00738.hp1 HG01071.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.543+2045C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569692 | ||||||
| chr3:111569745
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.543+2098G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569745 | ||||||
| chr3:111569849
|
A | AC | 7 | a0001c0001t0001g0161a0001c0001t0001g0233a0001c0001t0001g0263others(4): Show | 7 | HG00621.hp2 HG02145.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+2207dupC | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 111569849 | |||||
| chr3:111569989
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.543+2342T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569989 | ||||||
| chr3:111570034
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.543+2387C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570034 | ||||||
| chr3:111570388
|
G | A | 3 | a0001c0001t0005g0047a0001c0001t0005g0070a0001c0001t0005g0071 | 3 | HG01106.hp1 HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.543+2741G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570388 | ||||||
| chr3:111570473
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.543+2826G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570473 | ||||||
| chr3:111570490
|
G | A | 22 | a0002c0002t0001g0026a0002c0002t0001g0027a0002c0002t0001g0028others(19): Show | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+2843G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570490 | ||||||
| chr3:111570641
|
G | A | 2 | a0001c0001t0002g0041a0001c0001t0020g0042 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.543+2994G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570641 | ||||||
| chr3:111570713
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.543+3066A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570713 | ||||||
| chr3:111570850
|
G | A | 1 | a0001c0001t0022g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.543+3203G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570850 | ||||||
| chr3:111570946
|
T | C | 29 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0003g0003others(26): Show | 31 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.543+3299T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570946 | ||||||
| chr3:111570980
|
A | G | 183 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0043others(180): Show | 187 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.543+3333A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570980 | ||||||
| chr3:111571141
|
C | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(55): Show | 64 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.543+3494C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571141 | ||||||
| chr3:111571201
|
T | G | 3 | a0001c0001t0001g0261a0001c0001t0002g0262a0001c0001t0014g0059 | 3 | HG00438.hp1 HG03453.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.543+3554T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571201 | ||||||
| chr3:111571220
|
GT | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(219): Show | 231 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.543+3585delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 111571220 | |||||
| chr3:111571221
|
T | G | 1 | a0002c0002t0006g0021 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.543+3574T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571221 | ||||||
| chr3:111571231
|
T | G | 1 | a0001c0001t0002g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.543+3584T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571231 | ||||||
| chr3:111571260
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.543+3613C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571260 | ||||||
| chr3:111571284
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.543+3637T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571284 | ||||||
| chr3:111571292
|
A | C | 1 | a0001c0001t0002g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.543+3645A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571292 | ||||||
| chr3:111571304
|
A | T | 1 | a0001c0001t0002g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.543+3657A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571304 | ||||||
| chr3:111571375
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.543+3728A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571375 | ||||||
| chr3:111571565
|
G | T | 5 | a0001c0001t0002g0014a0001c0001t0003g0003a0001c0001t0003g0011others(2): Show | 6 | HG02809.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+3918G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571565 | ||||||
| chr3:111572194
|
A | C | 1 | a0001c0001t0002g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.543+4547A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572194 | ||||||
| chr3:111572197
|
T | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0122others(3): Show | 9 | HG02027.hp1 HG02074.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.543+4550T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572197 | ||||||
| chr3:111572235
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.543+4588A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572235 | ||||||
| chr3:111572256
|
A | G | 1 | a0002c0002t0002g0017 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.543+4609A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572256 | ||||||
| chr3:111572285
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0021g0061 | 2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.543+4638C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572285 | ||||||
| chr3:111572491
|
A | T | 1 | a0002c0002t0002g0173 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.543+4844A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572491 | ||||||
| chr3:111572492
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.543+4845T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572492 | ||||||
| chr3:111572499
|
G | T | 1 | a0001c0001t0002g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.543+4852G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572499 | ||||||
| chr3:111572582
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.543+4935A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572582 | ||||||
| chr3:111572617
|
A | C | 1 | a0001c0001t0007g0187 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.543+4970A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572617 | ||||||
| chr3:111572848
|
C | T | 159 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0043others(156): Show | 162 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.543+5201C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572848 | ||||||
| chr3:111572924
|
C | T | 1 | a0001c0001t0002g0142 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.543+5277C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572924 | ||||||
| chr3:111572952
|
C | T | 1 | a0002c0002t0002g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.543+5305C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572952 | ||||||
| chr3:111572966
|
A | G | 1 | a0001c0001t0014g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.543+5319A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572966 | ||||||
| chr3:111573056
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.543+5409G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573056 | ||||||
| chr3:111573099
|
C | T | 161 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0043others(158): Show | 164 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.543+5452C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573099 | ||||||
| chr3:111573254
|
A | G | 1 | a0001c0001t0020g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.543+5607A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573254 | ||||||
| chr3:111573369
|
A | T | 1 | a0001c0001t0001g0260 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.544-5658A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573369 | ||||||
| chr3:111573398
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0004g0159 | 2 | HG02738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.544-5629C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573398 | ||||||
| chr3:111573746
|
T | A | 1 | a0001c0001t0002g0132 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.544-5281T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573746 | ||||||
| chr3:111573930
|
G | T | 2 | a0001c0001t0001g0218a0001c0001t0016g0087 | 2 | NA18951.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.544-5097G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573930 | ||||||
| chr3:111573936
|
A | G | 1 | a0001c0001t0007g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.544-5091A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573936 | ||||||
| chr3:111574015
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.544-5012T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574015 | ||||||
| chr3:111574032
|
G | A | 6 | a0001c0001t0001g0129a0001c0001t0001g0236a0001c0001t0007g0130others(3): Show | 6 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-4995G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574032 | ||||||
| chr3:111574196
|
G | A | 1 | a0001c0001t0002g0288 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.544-4831G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574196 | ||||||
| chr3:111574228
|
C | T | 10 | a0001c0001t0001g0056a0001c0001t0002g0053a0001c0001t0002g0054others(7): Show | 10 | HG01192.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-4799C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574228 | ||||||
| chr3:111574243
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.544-4784G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574243 | ||||||
| chr3:111574348
|
A | G | 3 | a0001c0001t0005g0047a0001c0001t0005g0070a0001c0001t0005g0071 | 3 | HG01106.hp1 HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.544-4679A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574348 | ||||||
| chr3:111574763
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.544-4264T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574763 | ||||||
| chr3:111574776
|
A | C | 52 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0117others(49): Show | 52 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.544-4251A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574776 | ||||||
| chr3:111574778
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.544-4249G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574778 | ||||||
| chr3:111574788
|
A | AT | 55 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0117others(52): Show | 55 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.544-4227dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 111574788 | |||||
| chr3:111574830
|
C | T | 2 | a0001c0001t0002g0035a0001c0001t0014g0059 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.544-4197C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574830 | ||||||
| chr3:111574922
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.544-4105C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574922 | ||||||
| chr3:111574951
|
CT | C | 160 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0043others(157): Show | 163 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.544-4062delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 111574951 | |||||
| chr3:111575013
|
T | G | 1 | a0001c0001t0004g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.544-4014T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575013 | ||||||
| chr3:111575050
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.544-3977T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575050 | ||||||
| chr3:111575154
|
G | A | 1 | a0008c0007t0002g0022 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.544-3873G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575154 | ||||||
| chr3:111575192
|
G | C | 6 | a0001c0001t0002g0014a0001c0001t0003g0003a0001c0001t0003g0011others(3): Show | 7 | HG02809.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.544-3835G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575192 | ||||||
| chr3:111575520
|
A | G | 21 | a0001c0001t0001g0052a0001c0001t0001g0134a0001c0001t0001g0138others(18): Show | 21 | HG02145.hp1 HG02486.hp2 HG02523.hp2 others(18): Show |
intron_variant | MODIFIER | c.544-3507A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575520 | ||||||
| chr3:111575527
|
C | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(251): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.544-3500C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575527 | ||||||
| chr3:111575969
|
T | C | 1 | a0001c0001t0002g0088 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.544-3058T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575969 | ||||||
| chr3:111575972
|
A | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(281): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.544-3055A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575972 | ||||||
| chr3:111576400
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.544-2627T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111576400 | ||||||
| chr3:111576446
|
G | T | 2 | a0001c0003t0001g0020a0001c0003t0001g0146 | 2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.544-2581G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111576446 | ||||||
| chr3:111576478
|
A | G | 1 | a0001c0001t0001g0285 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.544-2549A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111576478 | ||||||
| chr3:111576495
|
C | A | 1 | a0001c0001t0001g0174 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.544-2532C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111576495 | ||||||
| chr3:111576974
|
C | T | 1 | a0002c0002t0002g0175 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.544-2053C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111576974 | ||||||
| chr3:111577000
|
A | G | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.544-2027A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111577000 | ||||||
| chr3:111577341
|
G | T | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.544-1686G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111577341 | ||||||
| chr3:111577348
|
G | A | 1 | a0002c0002t0002g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.544-1679G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111577348 | ||||||
| chr3:111577907
|
C | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(44): Show | 53 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.544-1120C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111577907 | ||||||
| chr3:111578116
|
C | G | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.544-911C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578116 | ||||||
| chr3:111578177
|
G | A | 2 | a0001c0001t0003g0003a0001c0001t0003g0016 | 3 | HG02809.hp1 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.544-850G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578177 | ||||||
| chr3:111578267
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(225): Show | 238 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.544-760A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578267 | ||||||
| chr3:111578288
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0002g0035 | 2 | HG03098.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.544-739C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578288 | ||||||
| chr3:111578302
|
G | A | 7 | a0001c0001t0001g0271a0001c0001t0001g0287a0001c0001t0008g0009others(4): Show | 8 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-725G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578302 | ||||||
| chr3:111578449
|
T | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(225): Show | 238 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.544-578T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578449 | ||||||
| chr3:111578493
|
C | T | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.544-534C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578493 | ||||||
| chr3:111578680
|
G | A | 3 | a0001c0001t0002g0014a0001c0001t0002g0072a0001c0001t0005g0062 | 3 | HG02896.hp2 HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.544-347G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578680 | ||||||
| chr3:111578870
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-157A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578870 | ||||||
| chr3:111579298
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(46): Show | 55 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.751+64A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111579298 | ||||||
| chr3:111579447
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.751+213C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111579447 | ||||||
| chr3:111579698
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.751+464T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111579698 | ||||||
| chr3:111579795
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.751+561T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111579795 | ||||||
| chr3:111579921
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.751+687A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111579921 | ||||||
| chr3:111580175
|
G | A | 2 | a0002c0002t0001g0032a0002c0002t0002g0023 | 2 | HG04184.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.751+941G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580175 | ||||||
| chr3:111580229
|
A | G | 6 | a0001c0001t0001g0186a0001c0001t0001g0205a0001c0001t0001g0209others(3): Show | 6 | HG00639.hp2 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.751+995A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580229 | ||||||
| chr3:111580315
|
A | G | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.751+1081A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580315 | ||||||
| chr3:111580327
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.751+1093T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580327 | ||||||
| chr3:111580460
|
CAATT | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 224 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.751+1232_751+1235d others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 111580460 | |||||
| chr3:111580639
|
A | C | 1 | a0001c0001t0003g0066 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.751+1405A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580639 | ||||||
| chr3:111580673
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.751+1439C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580673 | ||||||
| chr3:111580764
|
G | A | 1 | a0001c0001t0010g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.751+1530G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580764 | ||||||
| chr3:111580821
|
T | G | 6 | a0001c0001t0009g0040a0001c0001t0009g0049a0001c0001t0009g0050others(3): Show | 6 | HG01192.hp2 HG02055.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.751+1587T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580821 | ||||||
| chr3:111581036
|
C | A | 1 | a0001c0001t0012g0008 | 2 | HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.751+1802C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581036 | ||||||
| chr3:111581060
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.751+1826T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581060 | ||||||
| chr3:111581066
|
T | C | 1 | a0001c0001t0002g0136 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.751+1832T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581066 | ||||||
| chr3:111581168
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.751+1934C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581168 | ||||||
| chr3:111581618
|
G | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(46): Show | 55 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.751+2384G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581618 | ||||||
| chr3:111581648
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.751+2414C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581648 | ||||||
| chr3:111581741
|
T | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0122others(3): Show | 9 | HG02027.hp1 HG02074.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.751+2507T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581741 | ||||||
| chr3:111581775
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.751+2541G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581775 | ||||||
| chr3:111581850
|
C | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.751+2616C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581850 | ||||||
| chr3:111581928
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(197): Show | 209 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.751+2694G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581928 | ||||||
| chr3:111581975
|
C | CATAGGTT others(19): Show |
1 | a0001c0001t0001g0113 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.751+2743_751+2768d others(28): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 111581975 | |||||
| chr3:111581984
|
A | G | 15 | a0001c0001t0001g0224a0001c0001t0001g0233a0001c0001t0001g0241others(12): Show | 15 | HG00280.hp1 HG01496.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.751+2750A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581984 | ||||||
| chr3:111582309
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.752-3014T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111582309 | ||||||
| chr3:111582398
|
G | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0122others(3): Show | 9 | HG02027.hp1 HG02074.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.752-2925G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111582398 | ||||||
| chr3:111582611
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.752-2712G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111582611 | ||||||
| chr3:111582966
|
T | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(238): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.752-2357T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111582966 | ||||||
| chr3:111582996
|
A | C | 1 | a0001c0001t0002g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.752-2327A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111582996 | ||||||
| chr3:111583045
|
A | C | 6 | a0001c0001t0002g0041a0001c0001t0002g0147a0001c0001t0003g0048others(3): Show | 6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.752-2278A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583045 | ||||||
| chr3:111583064
|
C | T | 6 | a0001c0001t0002g0041a0001c0001t0002g0147a0001c0001t0003g0048others(3): Show | 6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.752-2259C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583064 | ||||||
| chr3:111583129
|
T | C | 2 | a0001c0001t0002g0014a0001c0001t0002g0072 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.752-2194T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583129 | ||||||
| chr3:111583292
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(238): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.752-2031T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583292 | ||||||
| chr3:111583381
|
G | A | 13 | a0001c0001t0002g0063a0001c0001t0002g0085a0002c0002t0001g0026others(10): Show | 14 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.752-1942G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583381 | ||||||
| chr3:111583459
|
C | T | 1 | a0001c0001t0003g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.752-1864C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583459 | ||||||
| chr3:111583637
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0002g0014a0001c0001t0002g0072 | 3 | HG02896.hp2 HG02970.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.752-1686C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583637 | ||||||
| chr3:111583769
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.752-1554G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583769 | ||||||
| chr3:111583848
|
G | C | 1 | a0001c0001t0003g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.752-1475G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583848 | ||||||
| chr3:111583874
|
G | A | 2 | a0001c0001t0010g0046a0001c0001t0010g0099 | 2 | NA19077.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.752-1449G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583874 | ||||||
| chr3:111583944
|
G | A | 19 | a0001c0001t0001g0045a0001c0001t0001g0155a0001c0001t0001g0161others(16): Show | 19 | HG01071.hp2 HG01099.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.752-1379G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583944 | ||||||
| chr3:111583959
|
T | C | 2 | a0001c0003t0001g0020a0001c0003t0001g0146 | 2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.752-1364T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583959 | ||||||
| chr3:111583965
|
C | A | 1 | a0001c0001t0001g0010 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.752-1358C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583965 | ||||||
| chr3:111583975
|
G | T | 142 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0079others(139): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.752-1348G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583975 | ||||||
| chr3:111584063
|
G | T | 2 | a0001c0001t0002g0014a0001c0001t0002g0072 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.752-1260G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584063 | ||||||
| chr3:111584064
|
C | G | 2 | a0001c0001t0002g0014a0001c0001t0002g0072 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.752-1259C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584064 | ||||||
| chr3:111584078
|
C | G | 1 | a0001c0001t0003g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.752-1245C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584078 | ||||||
| chr3:111584387
|
C | T | 11 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.752-936C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584387 | ||||||
| chr3:111584430
|
G | A | 11 | a0001c0001t0001g0129a0001c0001t0001g0236a0001c0001t0003g0003others(8): Show | 12 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.752-893G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584430 | ||||||
| chr3:111584473
|
G | C | 6 | a0001c0001t0001g0129a0001c0001t0001g0236a0001c0001t0007g0130others(3): Show | 6 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.752-850G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584473 | ||||||
| chr3:111584538
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.752-785T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584538 | ||||||
| chr3:111584547
|
C | G | 1 | a0002c0002t0002g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.752-776C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584547 | ||||||
| chr3:111584631
|
G | A | 17 | a0001c0001t0001g0045a0001c0001t0001g0155a0001c0001t0001g0161others(14): Show | 17 | HG01071.hp2 HG01099.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.752-692G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584631 | ||||||
| chr3:111584644
|
C | T | 1 | a0001c0001t0003g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.752-679C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584644 | ||||||
| chr3:111584645
|
G | A | 1 | a0002c0002t0002g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.752-678G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584645 | ||||||
| chr3:111584647
|
G | A | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(261): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.752-676G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584647 | ||||||
| chr3:111584741
|
G | A | 8 | a0001c0001t0001g0129a0001c0001t0001g0223a0001c0001t0001g0236others(5): Show | 8 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.752-582G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584741 | ||||||
| chr3:111584820
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.752-503A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584820 | ||||||
| chr3:111584966
|
C | G | 1 | a0001c0001t0001g0004 | 2 | NA19004.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.752-357C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584966 | ||||||
| chr3:111584994
|
T | G | 14 | a0001c0001t0002g0035a0001c0001t0002g0063a0001c0001t0002g0085others(11): Show | 15 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.752-329T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584994 | ||||||
| chr3:111585116
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.752-207A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111585116 | ||||||
| chr3:111585228
|
A | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0217 | 2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.752-95A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111585228 | ||||||
| chr3:111585479
|
G | A | 1 | a0001c0001t0012g0008 | 2 | HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.807+101G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111585479 | ||||||
| chr3:111585613
|
G | GA | 7 | a0001c0001t0001g0129a0001c0001t0001g0236a0001c0001t0007g0130others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(4): Show |
intron_variant | MODIFIER | c.807+244dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111585613 | |||||
| chr3:111585642
|
C | T | 2 | a0001c0003t0001g0020a0001c0003t0001g0146 | 2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.807+264C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111585642 | ||||||
| chr3:111585650
|
T | C | 11 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.807+272T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111585650 | ||||||
| chr3:111585748
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.807+370G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111585748 | ||||||
| chr3:111585787
|
T | C | 102 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0079others(99): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.807+409T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111585787 | ||||||
| chr3:111585967
|
C | T | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.807+589C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111585967 | ||||||
| chr3:111586003
|
C | T | 4 | a0001c0001t0001g0134a0001c0001t0002g0005a0001c0001t0003g0005others(1): Show | 4 | HG03491.hp1 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+625C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586003 | ||||||
| chr3:111586030
|
A | G | 1 | a0007c0008t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.807+652A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586030 | ||||||
| chr3:111586307
|
G | T | 1 | a0001c0001t0001g0244 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.807+929G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586307 | ||||||
| chr3:111586620
|
G | A | 25 | a0001c0001t0001g0012a0001c0001t0001g0134a0001c0001t0002g0005others(22): Show | 25 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.807+1242G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586620 | ||||||
| chr3:111586735
|
C | G | 3 | a0001c0001t0001g0284a0001c0001t0001g0285a0004c0009t0001g0243 | 3 | HG02132.hp1 NA18999.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.807+1357C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586735 | ||||||
| chr3:111586780
|
C | G | 2 | a0001c0001t0002g0041a0001c0001t0020g0042 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.807+1402C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586780 | ||||||
| chr3:111586818
|
A | G | 1 | a0001c0001t0005g0188 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.807+1440A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586818 | ||||||
| chr3:111587009
|
C | T | 11 | a0001c0001t0001g0129a0001c0001t0001g0236a0001c0001t0003g0003others(8): Show | 12 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.807+1631C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587009 | ||||||
| chr3:111587033
|
T | G | 3 | a0001c0001t0005g0047a0001c0001t0005g0070a0001c0001t0005g0071 | 3 | HG01106.hp1 HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.807+1655T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587033 | ||||||
| chr3:111587065
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.807+1687G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587065 | ||||||
| chr3:111587100
|
C | T | 1 | a0001c0001t0016g0087 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.807+1722C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587100 | ||||||
| chr3:111587167
|
A | T | 1 | a0001c0001t0002g0227 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.807+1789A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587167 | ||||||
| chr3:111587499
|
G | A | 1 | a0001c0001t0025g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.807+2121G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587499 | ||||||
| chr3:111587513
|
G | A | 25 | a0001c0001t0001g0012a0001c0001t0001g0134a0001c0001t0002g0005others(22): Show | 25 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.807+2135G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587513 | ||||||
| chr3:111587540
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.807+2162T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587540 | ||||||
| chr3:111587635
|
G | C | 25 | a0001c0001t0001g0012a0001c0001t0001g0134a0001c0001t0002g0005others(22): Show | 25 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.807+2257G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587635 | ||||||
| chr3:111587657
|
C | T | 7 | a0001c0001t0001g0129a0001c0001t0001g0236a0001c0001t0007g0130others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(4): Show |
intron_variant | MODIFIER | c.807+2279C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587657 | ||||||
| chr3:111587658
|
G | A | 3 | a0002c0002t0001g0026a0002c0002t0002g0024a0002c0002t0002g0025 | 3 | HG01952.hp2 NA19058.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.807+2280G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587658 | ||||||
| chr3:111587689
|
G | A | 1 | a0001c0001t0002g0121 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.807+2311G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587689 | ||||||
| chr3:111587694
|
C | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(252): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.807+2316C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587694 | ||||||
| chr3:111587695
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.807+2317C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587695 | ||||||
| chr3:111587713
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.807+2335G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587713 | ||||||
| chr3:111587853
|
C | G | 3 | a0001c0001t0002g0147a0001c0001t0003g0048a0001c0001t0003g0148 | 3 | HG02109.hp2 HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.807+2475C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587853 | ||||||
| chr3:111587993
|
C | A | 4 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(1): Show | 5 | HG02809.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.807+2615C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587993 | ||||||
| chr3:111588199
|
A | G | 94 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0079others(91): Show | 96 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.807+2821A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588199 | ||||||
| chr3:111588378
|
G | A | 3 | a0001c0001t0005g0190a0001c0001t0005g0191a0001c0001t0005g0192 | 3 | HG02922.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.807+3000G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588378 | ||||||
| chr3:111588432
|
C | G | 101 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0079others(98): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.807+3054C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588432 | ||||||
| chr3:111588471
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.807+3093G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588471 | ||||||
| chr3:111588509
|
C | G | 19 | a0001c0001t0001g0129a0001c0001t0001g0236a0001c0001t0003g0003others(16): Show | 20 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.807+3131C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588509 | ||||||
| chr3:111588814
|
A | T | 1 | a0001c0001t0025g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.807+3436A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588814 | ||||||
| chr3:111588931
|
G | C | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.807+3553G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588931 | ||||||
| chr3:111588953
|
T | C | 1 | a0002c0002t0002g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.807+3575T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588953 | ||||||
| chr3:111588954
|
CT | C | 7 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0253others(4): Show | 7 | HG00733.hp2 HG00735.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.807+3591delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111588954 | |||||
| chr3:111588954
|
CTT | C | 41 | a0001c0001t0001g0012a0001c0001t0001g0134a0001c0001t0002g0005others(38): Show | 42 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.807+3590_807+3591d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111588954 | |||||
| chr3:111588957
|
T | G | 1 | a0001c0001t0003g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.807+3579T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588957 | ||||||
| chr3:111589151
|
C | T | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.807+3773C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589151 | ||||||
| chr3:111589172
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(260): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.807+3794A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589172 | ||||||
| chr3:111589193
|
G | A | 12 | a0001c0001t0001g0129a0001c0001t0001g0236a0001c0001t0003g0003others(9): Show | 13 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.807+3815G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589193 | ||||||
| chr3:111589196
|
C | T | 6 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0038others(3): Show | 6 | HG02257.hp2 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.807+3818C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589196 | ||||||
| chr3:111589250
|
T | A | 25 | a0001c0001t0001g0012a0001c0001t0001g0134a0001c0001t0002g0005others(22): Show | 25 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.807+3872T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589250 | ||||||
| chr3:111589552
|
G | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.807+4174G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589552 | ||||||
| chr3:111589721
|
A | G | 12 | a0001c0001t0001g0129a0001c0001t0001g0236a0001c0001t0003g0003others(9): Show | 13 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.807+4343A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589721 | ||||||
| chr3:111589887
|
A | T | 29 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0155others(26): Show | 29 | HG00438.hp2 HG00609.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.807+4509A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589887 | ||||||
| chr3:111589897
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.807+4519C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589897 | ||||||
| chr3:111589903
|
C | T | 23 | a0001c0001t0001g0012a0001c0001t0001g0134a0001c0001t0002g0005others(20): Show | 23 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.807+4525C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589903 | ||||||
| chr3:111589937
|
A | T | 1 | a0001c0001t0001g0244 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.807+4559A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589937 | ||||||
| chr3:111590132
|
C | T | 1 | a0001c0001t0006g0201 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.807+4754C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590132 | ||||||
| chr3:111590249
|
C | T | 1 | a0007c0008t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.807+4871C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590249 | ||||||
| chr3:111590377
|
A | G | 95 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0079others(92): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.807+4999A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590377 | ||||||
| chr3:111590543
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.807+5165C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590543 | ||||||
| chr3:111590683
|
T | A | 1 | a0001c0001t0001g0091 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.807+5305T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590683 | ||||||
| chr3:111590825
|
G | C | 17 | a0001c0001t0001g0134a0001c0001t0002g0005a0001c0001t0002g0089others(14): Show | 17 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.807+5447G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590825 | ||||||
| chr3:111590832
|
A | C | 41 | a0001c0001t0001g0012a0001c0001t0001g0134a0001c0001t0002g0005others(38): Show | 42 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.807+5454A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590832 | ||||||
| chr3:111590909
|
C | T | 1 | a0001c0001t0003g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.807+5531C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590909 | ||||||
| chr3:111590938
|
C | T | 22 | a0001c0001t0001g0012a0001c0001t0001g0134a0001c0001t0002g0005others(19): Show | 22 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.807+5560C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590938 | ||||||
| chr3:111591021
|
C | T | 22 | a0001c0001t0001g0012a0001c0001t0001g0134a0001c0001t0002g0005others(19): Show | 22 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.807+5643C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591021 | ||||||
| chr3:111591022
|
A | T | 14 | a0001c0001t0002g0035a0001c0001t0002g0063a0001c0001t0002g0085others(11): Show | 15 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.807+5644A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591022 | ||||||
| chr3:111591098
|
G | A | 1 | a0001c0001t0014g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.807+5720G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591098 | ||||||
| chr3:111591150
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.807+5772G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591150 | ||||||
| chr3:111591189
|
G | A | 1 | a0004c0009t0001g0243 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.807+5811G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591189 | ||||||
| chr3:111591368
|
T | TC | 18 | a0001c0001t0001g0252a0001c0001t0002g0035a0001c0001t0002g0147others(15): Show | 19 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.807+5991dupC | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111591368 | |||||
| chr3:111591370
|
T | C | 108 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0079others(105): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.807+5992T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591370 | ||||||
| chr3:111591371
|
T | A | 18 | a0001c0001t0001g0252a0001c0001t0002g0035a0001c0001t0002g0147others(15): Show | 19 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.807+5993T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591371 | ||||||
| chr3:111591371
|
T | TA | 13 | a0001c0001t0002g0089a0001c0001t0002g0139a0001c0001t0003g0003others(10): Show | 14 | HG02055.hp1 HG02647.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.807+6017dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111591371 | |||||
| chr3:111591371
|
T | TAA | 93 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0043others(90): Show | 96 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.807+6016_807+6017d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111591371 | |||||
| chr3:111591371
|
T | TAAA | 14 | a0001c0001t0001g0115a0001c0001t0001g0224a0001c0001t0001g0233others(11): Show | 14 | HG00280.hp1 HG01496.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.807+6015_807+6017d others(5): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111591371 | |||||
| chr3:111591371
|
TA | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(49): Show | 58 | HG00609.hp1 HG00621.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.807+6017delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111591371 | |||||
| chr3:111591371
|
TAA | T | 35 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0097others(32): Show | 35 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.807+6016_807+6017d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111591371 | |||||
| chr3:111591939
|
C | A | 1 | a0001c0001t0008g0270 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.808-6181C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591939 | ||||||
| chr3:111592141
|
A | C | 7 | a0001c0001t0001g0129a0001c0001t0001g0236a0001c0001t0007g0130others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(4): Show |
intron_variant | MODIFIER | c.808-5979A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111592141 | ||||||
| chr3:111592328
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.808-5792A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111592328 | ||||||
| chr3:111592567
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.808-5553A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111592567 | ||||||
| chr3:111592573
|
GTC | G | 13 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0038others(10): Show | 13 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.808-5541_808-5540d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111592573 | |||||
| chr3:111592610
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0004g0153 | 2 | HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.808-5510A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111592610 | ||||||
| chr3:111592980
|
A | G | 1 | a0001c0001t0003g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.808-5140A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111592980 | ||||||
| chr3:111593296
|
T | C | 1 | a0001c0001t0004g0162 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.808-4824T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593296 | ||||||
| chr3:111593331
|
A | G | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.808-4789A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593331 | ||||||
| chr3:111593339
|
G | A | 3 | a0001c0003t0001g0020a0001c0003t0001g0146a0003c0006t0005g0166 | 3 | HG02717.hp2 HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.808-4781G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593339 | ||||||
| chr3:111593458
|
T | C | 15 | a0001c0001t0001g0134a0001c0001t0002g0005a0001c0001t0002g0089others(12): Show | 15 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.808-4662T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593458 | ||||||
| chr3:111593497
|
C | G | 1 | a0001c0001t0004g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.808-4623C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593497 | ||||||
| chr3:111593598
|
A | G | 4 | a0001c0001t0002g0147a0001c0001t0003g0048a0001c0001t0003g0148others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.808-4522A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593598 | ||||||
| chr3:111593966
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.808-4154C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593966 | ||||||
| chr3:111594118
|
A | T | 14 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.808-4002A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594118 | ||||||
| chr3:111594233
|
G | A | 1 | a0002c0002t0002g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.808-3887G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594233 | ||||||
| chr3:111594495
|
C | A | 1 | a0001c0001t0001g0202 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.808-3625C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594495 | ||||||
| chr3:111594572
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.808-3548C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594572 | ||||||
| chr3:111594610
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.808-3510T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594610 | ||||||
| chr3:111594682
|
G | A | 1 | a0001c0001t0003g0013 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.808-3438G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594682 | ||||||
| chr3:111594695
|
G | C | 1 | a0001c0004t0007g0237 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.808-3425G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594695 | ||||||
| chr3:111595007
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(255): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.808-3113C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111595007 | ||||||
| chr3:111595281
|
G | A | 15 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0038others(12): Show | 15 | HG02145.hp1 HG02257.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.808-2839G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111595281 | ||||||
| chr3:111595490
|
C | T | 1 | a0002c0002t0002g0023 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.808-2630C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111595490 | ||||||
| chr3:111595524
|
C | G | 1 | a0001c0001t0001g0245 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.808-2596C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111595524 | ||||||
| chr3:111595662
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.808-2458A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111595662 | ||||||
| chr3:111595794
|
G | C | 1 | a0001c0001t0010g0099 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.808-2326G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111595794 | ||||||
| chr3:111596151
|
G | A | 1 | a0001c0001t0016g0087 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.808-1969G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596151 | ||||||
| chr3:111596161
|
C | CA | 93 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0079others(90): Show | 96 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.808-1952dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111596161 | |||||
| chr3:111596219
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1901G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596219 | ||||||
| chr3:111596268
|
G | GA | 4 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0100others(1): Show | 6 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.808-1844dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111596268 | |||||
| chr3:111596350
|
A | C | 1 | a0001c0001t0025g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.808-1770A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596350 | ||||||
| chr3:111596463
|
G | A | 2 | a0001c0001t0011g0172a0001c0001t0011g0279 | 2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.808-1657G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596463 | ||||||
| chr3:111596615
|
A | C | 1 | a0001c0001t0001g0097 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.808-1505A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596615 | ||||||
| chr3:111596793
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1327T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596793 | ||||||
| chr3:111596958
|
A | G | 11 | a0001c0001t0001g0224a0001c0001t0001g0233a0001c0001t0001g0241others(8): Show | 11 | HG01496.hp2 HG02132.hp1 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.808-1162A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596958 | ||||||
| chr3:111597517
|
G | A | 17 | a0001c0001t0001g0236a0001c0001t0003g0003a0001c0001t0003g0011others(14): Show | 18 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.808-603G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111597517 | ||||||
| chr3:111597571
|
C | T | 3 | a0001c0001t0003g0148a0001c0001t0014g0059a0001c0001t0020g0042 | 3 | HG02559.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.808-549C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111597571 | ||||||
| chr3:111597651
|
G | A | 7 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0240others(4): Show | 7 | HG02083.hp1 HG02523.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.808-469G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111597651 | ||||||
| chr3:111597804
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.808-316T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111597804 | ||||||
| chr3:111597954
|
G | A | 5 | a0001c0001t0001g0223a0001c0001t0001g0247a0001c0001t0001g0255others(2): Show | 5 | HG00099.hp2 HG00323.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.808-166G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111597954 | ||||||
| chr3:111598039
|
C | CTTATG | 95 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(92): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.808-77_808-76insGT others(3): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111598039 | |||||
| chr3:111598401
|
A | G | 1 | a0001c0001t0004g0181 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.898+191A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111598401 | ||||||
| chr3:111598424
|
A | G | 1 | a0002c0002t0002g0017 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.898+214A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111598424 | ||||||
| chr3:111598863
|
G | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.898+653G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111598863 | ||||||
| chr3:111598923
|
A | G | 1 | a0001c0001t0008g0265 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.898+713A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111598923 | ||||||
| chr3:111598957
|
T | TTTTTA | 18 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(15): Show | 18 | HG02145.hp1 HG02486.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.898+772_898+776dup others(5): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 111598957 | |||||
| chr3:111598957
|
T | TTTTTATT others(3): Show |
1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.898+767_898+776dup others(10): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 111598957 | |||||
| chr3:111599009
|
C | G | 1 | a0001c0001t0001g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.898+799C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599009 | ||||||
| chr3:111599125
|
C | T | 5 | a0001c0001t0008g0009a0001c0001t0008g0143a0001c0001t0008g0264others(2): Show | 6 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.898+915C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599125 | ||||||
| chr3:111599158
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(53): Show | 62 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.898+948C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599158 | ||||||
| chr3:111599333
|
T | C | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.898+1123T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599333 | ||||||
| chr3:111599373
|
A | T | 1 | a0001c0001t0003g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.898+1163A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599373 | ||||||
| chr3:111599445
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.898+1235C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599445 | ||||||
| chr3:111599479
|
G | A | 2 | a0001c0001t0006g0069a0001c0001t0006g0073 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.899-1247G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599479 | ||||||
| chr3:111599486
|
G | A | 18 | a0001c0001t0001g0236a0001c0001t0003g0003a0001c0001t0003g0011others(15): Show | 19 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.899-1240G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599486 | ||||||
| chr3:111599546
|
C | G | 2 | a0001c0001t0006g0069a0001c0001t0006g0073 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.899-1180C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599546 | ||||||
| chr3:111599677
|
C | T | 89 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0079others(86): Show | 92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.899-1049C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599677 | ||||||
| chr3:111599678
|
G | A | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.899-1048G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599678 | ||||||
| chr3:111599865
|
T | G | 7 | a0001c0001t0005g0039a0001c0001t0009g0040a0001c0001t0009g0049others(4): Show | 7 | HG01192.hp2 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.899-861T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599865 | ||||||
| chr3:111600074
|
C | T | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.899-652C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111600074 | ||||||
| chr3:111600093
|
G | A | 3 | a0001c0001t0003g0148a0001c0001t0014g0059a0001c0001t0020g0042 | 3 | HG02559.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.899-633G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111600093 | ||||||
| chr3:111600186
|
C | T | 8 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.899-540C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111600186 | ||||||
| chr3:111600515
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.899-211C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111600515 | ||||||
| chr3:111600517
|
C | G | 3 | a0001c0001t0002g0158a0001c0001t0002g0249a0001c0001t0002g0250 | 3 | HG01168.hp2 HG01169.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.899-209C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111600517 | ||||||
| chr3:111600631
|
A | G | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.899-95A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111600631 | ||||||
| chr3:111601055
|
A | G | 3 | a0001c0001t0003g0148a0001c0001t0014g0059a0001c0001t0020g0042 | 3 | HG02559.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1087+141A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601055 | ||||||
| chr3:111601232
|
T | A | 1 | a0001c0001t0002g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1087+318T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601232 | ||||||
| chr3:111601256
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1087+342A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601256 | ||||||
| chr3:111601397
|
G | A | 2 | a0001c0001t0003g0211a0001c0001t0003g0213 | 2 | HG00438.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1087+483G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601397 | ||||||
| chr3:111601486
|
T | C | 1 | a0007c0008t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1087+572T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601486 | ||||||
| chr3:111601487
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1087+573C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601487 | ||||||
| chr3:111601532
|
A | G | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1087+618A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601532 | ||||||
| chr3:111602418
|
A | G | 1 | a0007c0008t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1087+1504A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602418 | ||||||
| chr3:111602504
|
C | A | 1 | a0001c0001t0002g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1087+1590C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602504 | ||||||
| chr3:111602531
|
T | G | 12 | a0001c0001t0002g0055a0001c0001t0002g0089a0001c0001t0002g0132others(9): Show | 12 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1087+1617T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602531 | ||||||
| chr3:111602572
|
C | T | 2 | a0001c0001t0006g0069a0001c0001t0006g0073 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1087+1658C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602572 | ||||||
| chr3:111602593
|
A | C | 1 | a0001c0001t0001g0127 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1087+1679A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602593 | ||||||
| chr3:111602689
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0253 | 2 | HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1087+1775A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602689 | ||||||
| chr3:111602732
|
T | C | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1087+1818T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602732 | ||||||
| chr3:111602742
|
G | A | 7 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(4): Show | 8 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1087+1828G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602742 | ||||||
| chr3:111603135
|
A | G | 28 | a0001c0001t0002g0005a0001c0001t0002g0078a0001c0001t0002g0081others(25): Show | 29 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.1087+2221A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111603135 | ||||||
| chr3:111603444
|
C | CA | 9 | a0001c0001t0001g0043a0001c0001t0001g0117a0001c0001t0001g0128others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.1087+2545dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | 111603444 | |||||
| chr3:111603444
|
CA | C | 21 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(18): Show | 22 | HG01081.hp1 HG02109.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1087+2545delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | 111603444 | |||||
| chr3:111603567
|
A | G | 15 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(12): Show | 16 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1087+2653A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111603567 | ||||||
| chr3:111603597
|
A | T | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1087+2683A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111603597 | ||||||
| chr3:111603861
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1088-2839C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111603861 | ||||||
| chr3:111603887
|
C | T | 8 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1088-2813C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111603887 | ||||||
| chr3:111603973
|
A | T | 3 | a0001c0001t0002g0089a0001c0001t0002g0132a0001c0001t0002g0135 | 3 | HG02735.hp2 HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1088-2727A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111603973 | ||||||
| chr3:111604007
|
A | G | 89 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(86): Show | 91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1088-2693A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604007 | ||||||
| chr3:111604157
|
G | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0232a0001c0001t0001g0248others(1): Show | 4 | HG02015.hp2 HG02080.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1088-2543G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604157 | ||||||
| chr3:111604172
|
C | T | 15 | a0001c0001t0001g0045a0001c0001t0004g0144a0001c0001t0004g0145others(12): Show | 15 | HG00735.hp1 HG01099.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1088-2528C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604172 | ||||||
| chr3:111604206
|
A | G | 14 | a0001c0001t0002g0035a0001c0001t0002g0055a0001c0001t0002g0089others(11): Show | 14 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1088-2494A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604206 | ||||||
| chr3:111604257
|
C | T | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1088-2443C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604257 | ||||||
| chr3:111604264
|
A | T | 90 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0079others(87): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1088-2436A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604264 | ||||||
| chr3:111604588
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0018g0133 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1088-2112C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604588 | ||||||
| chr3:111604602
|
A | C | 3 | a0001c0001t0001g0094a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG01358.hp2 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1088-2098A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604602 | ||||||
| chr3:111604887
|
A | AG | 38 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0041others(35): Show | 39 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1088-1810dupG | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | 111604887 | |||||
| chr3:111604887
|
A | G | 1 | a0001c0001t0002g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1088-1813A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604887 | ||||||
| chr3:111604893
|
A | G | 10 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(7): Show | 10 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1088-1807A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604893 | ||||||
| chr3:111604900
|
G | T | 3 | a0001c0001t0009g0049a0001c0001t0009g0050a0001c0001t0009g0051 | 3 | HG01192.hp2 HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1088-1800G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604900 | ||||||
| chr3:111604963
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1088-1737A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604963 | ||||||
| chr3:111605379
|
G | A | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088-1321G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111605379 | ||||||
| chr3:111605582
|
C | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0253 | 2 | HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1088-1118C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111605582 | ||||||
| chr3:111605618
|
C | A | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1088-1082C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111605618 | ||||||
| chr3:111605618
|
C | T | 1 | a0001c0001t0005g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1088-1082C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111605618 | ||||||
| chr3:111605942
|
A | G | 3 | a0001c0001t0001g0220a0001c0001t0001g0263a0002c0002t0001g0277 | 3 | HG00621.hp2 NA18953.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1088-758A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111605942 | ||||||
| chr3:111606007
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0208 | 3 | HG02698.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1088-693C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111606007 | ||||||
| chr3:111606124
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1088-576C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111606124 | ||||||
| chr3:111606129
|
G | A | 5 | a0001c0001t0001g0077a0001c0001t0001g0091a0001c0001t0001g0103others(2): Show | 5 | NA18952.hp2 NA18961.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1088-571G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111606129 | ||||||
| chr3:111606333
|
A | T | 1 | a0001c0001t0002g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1088-367A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111606333 | ||||||
| chr3:111606628
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1088-72A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111606628 | ||||||
| chr3:111607548
|
C | T | 1 | a0001c0001t0022g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1180+756C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111607548 | ||||||
| chr3:111607691
|
G | A | 90 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0079others(87): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1180+899G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111607691 | ||||||
| chr3:111607875
|
T | C | 85 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(82): Show | 87 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1180+1083T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111607875 | ||||||
| chr3:111607876
|
G | A | 2 | a0003c0006t0003g0165a0003c0006t0003g0167 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1180+1084G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111607876 | ||||||
| chr3:111608009
|
A | G | 3 | a0001c0001t0003g0148a0001c0001t0014g0059a0001c0001t0020g0042 | 3 | HG02559.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1180+1217A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111608009 | ||||||
| chr3:111608106
|
T | TTGGCTGA others(39): Show |
14 | a0001c0001t0002g0035a0001c0001t0002g0055a0001c0001t0002g0089others(11): Show | 14 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1180+1355_1180+135 others(50): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111608106 | |||||
| chr3:111608139
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1180+1347T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111608139 | ||||||
| chr3:111608484
|
T | G | 1 | a0001c0001t0009g0049 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1180+1692T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111608484 | ||||||
| chr3:111608514
|
G | C | 7 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(4): Show | 8 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180+1722G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111608514 | ||||||
| chr3:111608652
|
A | G | 10 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(7): Show | 10 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1180+1860A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111608652 | ||||||
| chr3:111609063
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1180+2271C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609063 | ||||||
| chr3:111609205
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0100others(1): Show | 6 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180+2413G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609205 | ||||||
| chr3:111609213
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1180+2421G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609213 | ||||||
| chr3:111609273
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1180+2481G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609273 | ||||||
| chr3:111609554
|
T | C | 1 | a0001c0001t0007g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1180+2762T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609554 | ||||||
| chr3:111609591
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1180+2799A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609591 | ||||||
| chr3:111609711
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1180+2919A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609711 | ||||||
| chr3:111609751
|
G | A | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180+2959G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609751 | ||||||
| chr3:111610077
|
C | T | 1 | a0001c0001t0014g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1180+3285C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610077 | ||||||
| chr3:111610085
|
A | G | 8 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1180+3293A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610085 | ||||||
| chr3:111610188
|
T | G | 1 | a0002c0002t0002g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1180+3396T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610188 | ||||||
| chr3:111610247
|
T | A | 1 | a0001c0001t0001g0245 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1180+3455T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610247 | ||||||
| chr3:111610283
|
T | C | 1 | a0001c0001t0004g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1180+3491T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610283 | ||||||
| chr3:111610387
|
G | A | 5 | a0001c0001t0001g0052a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180+3595G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610387 | ||||||
| chr3:111610877
|
C | T | 1 | a0001c0001t0003g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1180+4085C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610877 | ||||||
| chr3:111610935
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1180+4143G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610935 | ||||||
| chr3:111610952
|
G | C | 15 | a0001c0001t0001g0045a0001c0001t0004g0144a0001c0001t0004g0145others(12): Show | 15 | HG00735.hp1 HG01099.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1180+4160G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610952 | ||||||
| chr3:111611164
|
T | C | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1180+4372T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611164 | ||||||
| chr3:111611214
|
G | T | 85 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(82): Show | 87 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1180+4422G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611214 | ||||||
| chr3:111611289
|
A | G | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180+4497A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611289 | ||||||
| chr3:111611407
|
G | T | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1180+4615G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611407 | ||||||
| chr3:111611551
|
A | G | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1180+4759A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611551 | ||||||
| chr3:111611629
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1180+4837A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611629 | ||||||
| chr3:111611718
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1180+4926G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611718 | ||||||
| chr3:111611856
|
G | T | 1 | a0001c0014t0001g0095 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1180+5064G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611856 | ||||||
| chr3:111611879
|
T | G | 2 | a0001c0001t0002g0053a0001c0001t0002g0054 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1180+5087T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611879 | ||||||
| chr3:111612075
|
C | T | 89 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(86): Show | 91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1180+5283C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111612075 | ||||||
| chr3:111612107
|
A | G | 37 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0053others(34): Show | 38 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1180+5315A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111612107 | ||||||
| chr3:111612628
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1180+5836G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111612628 | ||||||
| chr3:111612999
|
T | C | 1 | a0001c0015t0001g0119 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1180+6207T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111612999 | ||||||
| chr3:111613436
|
G | A | 10 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(7): Show | 10 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1180+6644G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111613436 | ||||||
| chr3:111613514
|
A | G | 10 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(7): Show | 10 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1180+6722A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111613514 | ||||||
| chr3:111613546
|
G | C | 85 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(82): Show | 87 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1180+6754G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111613546 | ||||||
| chr3:111613610
|
A | T | 2 | a0001c0001t0002g0249a0001c0001t0002g0250 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1180+6818A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111613610 | ||||||
| chr3:111613717
|
C | T | 8 | a0001c0001t0004g0149a0001c0001t0004g0153a0001c0001t0004g0154others(5): Show | 8 | HG01099.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180+6925C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111613717 | ||||||
| chr3:111613956
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1180+7164A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111613956 | ||||||
| chr3:111614186
|
A | G | 1 | a0001c0001t0005g0204 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1180+7394A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614186 | ||||||
| chr3:111614414
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1180+7622G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614414 | ||||||
| chr3:111614441
|
T | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180+7649T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614441 | ||||||
| chr3:111614551
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1180+7759G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614551 | ||||||
| chr3:111614707
|
G | A | 6 | a0001c0001t0006g0185a0001c0001t0006g0200a0001c0001t0006g0201others(3): Show | 6 | HG01074.hp1 HG02559.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180+7915G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614707 | ||||||
| chr3:111614733
|
T | G | 1 | a0001c0001t0005g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1180+7941T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614733 | ||||||
| chr3:111614905
|
C | G | 1 | a0007c0008t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1180+8113C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614905 | ||||||
| chr3:111615008
|
C | A | 1 | a0001c0001t0022g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1180+8216C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615008 | ||||||
| chr3:111615070
|
G | A | 3 | a0001c0001t0002g0053a0001c0001t0002g0054a0002c0002t0002g0198 | 3 | HG02258.hp2 HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1180+8278G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615070 | ||||||
| chr3:111615117
|
C | T | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1180+8325C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615117 | ||||||
| chr3:111615177
|
G | A | 14 | a0001c0001t0002g0035a0001c0001t0002g0055a0001c0001t0002g0089others(11): Show | 14 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1180+8385G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615177 | ||||||
| chr3:111615267
|
C | T | 10 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(7): Show | 10 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1180+8475C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615267 | ||||||
| chr3:111615381
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1181-8373C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615381 | ||||||
| chr3:111615741
|
G | A | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181-8013G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615741 | ||||||
| chr3:111615809
|
C | G | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-7945C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615809 | ||||||
| chr3:111616112
|
C | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7642C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616112 | ||||||
| chr3:111616114
|
C | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7640C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616114 | ||||||
| chr3:111616116
|
T | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7638T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616116 | ||||||
| chr3:111616117
|
T | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7637T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616117 | ||||||
| chr3:111616118
|
T | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7636T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616118 | ||||||
| chr3:111616122
|
C | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7632C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616122 | ||||||
| chr3:111616124
|
C | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7630C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616124 | ||||||
| chr3:111616125
|
C | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7629C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616125 | ||||||
| chr3:111616128
|
C | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7626C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616128 | ||||||
| chr3:111616144
|
T | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7610T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616144 | ||||||
| chr3:111616155
|
C | T | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7599C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616155 | ||||||
| chr3:111616159
|
C | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7595C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616159 | ||||||
| chr3:111616160
|
A | AT | 18 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1181-7593dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111616160 | |||||
| chr3:111616175
|
C | T | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7579C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616175 | ||||||
| chr3:111616185
|
C | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7569C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616185 | ||||||
| chr3:111616194
|
T | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7560T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616194 | ||||||
| chr3:111616206
|
T | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7548T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616206 | ||||||
| chr3:111616209
|
A | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7545A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616209 | ||||||
| chr3:111616212
|
G | T | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7542G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616212 | ||||||
| chr3:111616213
|
A | G | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7541A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616213 | ||||||
| chr3:111616223
|
A | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7531A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616223 | ||||||
| chr3:111616224
|
T | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7530T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616224 | ||||||
| chr3:111616226
|
A | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7528A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616226 | ||||||
| chr3:111616229
|
T | TCCCCCCC others(36): Show |
1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7525_1181-752 others(47): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616229 | ||||||
| chr3:111616231
|
G | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7523G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616231 | ||||||
| chr3:111616242
|
A | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7512A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616242 | ||||||
| chr3:111616244
|
A | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7510A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616244 | ||||||
| chr3:111616246
|
A | G | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7508A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616246 | ||||||
| chr3:111616256
|
A | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7498A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616256 | ||||||
| chr3:111616256
|
A | G | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-7498A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616256 | ||||||
| chr3:111616257
|
T | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7497T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616257 | ||||||
| chr3:111616258
|
A | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7496A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616258 | ||||||
| chr3:111616271
|
T | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7483T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616271 | ||||||
| chr3:111616272
|
C | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7482C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616272 | ||||||
| chr3:111616273
|
A | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7481A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616273 | ||||||
| chr3:111616278
|
A | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7476A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616278 | ||||||
| chr3:111616283
|
T | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7471T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616283 | ||||||
| chr3:111616284
|
T | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7470T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616284 | ||||||
| chr3:111616285
|
T | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7469T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616285 | ||||||
| chr3:111616289
|
A | C | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7465A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616289 | ||||||
| chr3:111616290
|
T | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7464T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616290 | ||||||
| chr3:111616324
|
T | A | 1 | a0001c0001t0018g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7430T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616324 | ||||||
| chr3:111616499
|
T | C | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-7255T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616499 | ||||||
| chr3:111616511
|
A | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(64): Show | 73 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1181-7243A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616511 | ||||||
| chr3:111616631
|
A | G | 29 | a0001c0001t0002g0005a0001c0001t0002g0078a0001c0001t0002g0081others(26): Show | 30 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.1181-7123A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616631 | ||||||
| chr3:111616656
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1181-7098G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616656 | ||||||
| chr3:111616711
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-7043G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616711 | ||||||
| chr3:111616751
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-7003G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616751 | ||||||
| chr3:111616809
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1181-6945C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616809 | ||||||
| chr3:111617205
|
G | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-6549G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617205 | ||||||
| chr3:111617323
|
A | G | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-6431A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617323 | ||||||
| chr3:111617460
|
G | A | 4 | a0001c0001t0009g0040a0001c0001t0009g0049a0001c0001t0009g0050others(1): Show | 4 | HG01192.hp2 HG02630.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181-6294G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617460 | ||||||
| chr3:111617571
|
A | G | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-6183A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617571 | ||||||
| chr3:111617605
|
T | A | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-6149T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617605 | ||||||
| chr3:111617885
|
T | C | 1 | a0001c0001t0002g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1181-5869T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617885 | ||||||
| chr3:111617900
|
G | A | 8 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1181-5854G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617900 | ||||||
| chr3:111618074
|
T | C | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-5680T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618074 | ||||||
| chr3:111618121
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1181-5633C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618121 | ||||||
| chr3:111618160
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-5594G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618160 | ||||||
| chr3:111618196
|
C | T | 1 | a0001c0001t0006g0201 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1181-5558C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618196 | ||||||
| chr3:111618311
|
T | C | 91 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(88): Show | 93 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1181-5443T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618311 | ||||||
| chr3:111618319
|
C | G | 1 | a0001c0001t0003g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1181-5435C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618319 | ||||||
| chr3:111618322
|
G | A | 2 | a0001c0001t0002g0035a0001c0011t0026g0036 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1181-5432G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618322 | ||||||
| chr3:111618429
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1181-5325C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618429 | ||||||
| chr3:111618444
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1181-5310G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618444 | ||||||
| chr3:111618461
|
T | C | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-5293T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618461 | ||||||
| chr3:111618581
|
T | C | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-5173T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618581 | ||||||
| chr3:111618581
|
TC | T | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-5172delC | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618581 | ||||||
| chr3:111618582
|
C | CT | 50 | a0001c0001t0001g0171a0001c0001t0001g0278a0001c0001t0002g0005others(47): Show | 51 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1181-5152dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111618582 | |||||
| chr3:111618582
|
CT | C | 36 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0128others(33): Show | 37 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1181-5152delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111618582 | |||||
| chr3:111618645
|
C | A | 1 | a0007c0008t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1181-5109C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618645 | ||||||
| chr3:111618817
|
C | T | 53 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0041others(50): Show | 54 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1181-4937C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618817 | ||||||
| chr3:111618851
|
A | G | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-4903A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618851 | ||||||
| chr3:111618863
|
G | A | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG00735.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1181-4891G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618863 | ||||||
| chr3:111619262
|
GT | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(270): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1181-4483delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111619262 | |||||
| chr3:111619322
|
G | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(58): Show | 67 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1181-4432G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619322 | ||||||
| chr3:111619465
|
G | A | 5 | a0001c0001t0008g0009a0001c0001t0008g0143a0001c0001t0008g0264others(2): Show | 6 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181-4289G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619465 | ||||||
| chr3:111619486
|
T | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(275): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1181-4268T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619486 | ||||||
| chr3:111619489
|
A | G | 91 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(88): Show | 93 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1181-4265A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619489 | ||||||
| chr3:111619629
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1181-4125T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619629 | ||||||
| chr3:111619647
|
A | C | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-4107A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619647 | ||||||
| chr3:111619665
|
T | C | 2 | a0001c0001t0003g0074a0001c0001t0021g0061 | 2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1181-4089T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619665 | ||||||
| chr3:111619731
|
TA | T | 11 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(8): Show | 11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1181-4019delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111619731 | |||||
| chr3:111619880
|
A | G | 1 | a0002c0002t0002g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1181-3874A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619880 | ||||||
| chr3:111619939
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1181-3815G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619939 | ||||||
| chr3:111620139
|
TC | T | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181-3612delC | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111620139 | |||||
| chr3:111620272
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1181-3482G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620272 | ||||||
| chr3:111620342
|
C | CA | 8 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1181-3404dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111620342 | |||||
| chr3:111620352
|
G | A | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1181-3402G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620352 | ||||||
| chr3:111620660
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0251 | 2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1181-3094G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620660 | ||||||
| chr3:111620661
|
A | C | 2 | a0001c0001t0001g0221a0001c0001t0001g0251 | 2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1181-3093A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620661 | ||||||
| chr3:111620662
|
G | C | 2 | a0001c0001t0001g0221a0001c0001t0001g0251 | 2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1181-3092G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620662 | ||||||
| chr3:111620846
|
C | T | 2 | a0001c0001t0011g0172a0001c0001t0011g0279 | 2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1181-2908C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620846 | ||||||
| chr3:111620960
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1181-2794A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620960 | ||||||
| chr3:111620978
|
A | G | 1 | a0001c0001t0009g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1181-2776A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620978 | ||||||
| chr3:111621119
|
T | G | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-2635T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111621119 | ||||||
| chr3:111621509
|
GA | G | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181-2243delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111621509 | |||||
| chr3:111621575
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1181-2179G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111621575 | ||||||
| chr3:111621753
|
C | T | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-2001C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111621753 | ||||||
| chr3:111622119
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1181-1635C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622119 | ||||||
| chr3:111622129
|
A | G | 29 | a0001c0001t0002g0005a0001c0001t0002g0078a0001c0001t0002g0081others(26): Show | 30 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.1181-1625A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622129 | ||||||
| chr3:111622156
|
G | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-1598G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622156 | ||||||
| chr3:111622202
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1181-1552G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622202 | ||||||
| chr3:111622410
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1181-1344A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622410 | ||||||
| chr3:111622425
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1181-1329T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622425 | ||||||
| chr3:111622441
|
G | A | 1 | a0002c0002t0006g0021 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1181-1313G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622441 | ||||||
| chr3:111622459
|
T | C | 1 | a0001c0001t0020g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1181-1295T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622459 | ||||||
| chr3:111622543
|
C | A | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-1211C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622543 | ||||||
| chr3:111622606
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1181-1148A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622606 | ||||||
| chr3:111622781
|
ATAAC | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-970_1181-967d others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111622781 | |||||
| chr3:111622917
|
G | T | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181-837G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622917 | ||||||
| chr3:111622938
|
G | A | 1 | a0001c0001t0006g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1181-816G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622938 | ||||||
| chr3:111623144
|
T | C | 1 | a0001c0001t0002g0147 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1181-610T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623144 | ||||||
| chr3:111623181
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1181-573C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623181 | ||||||
| chr3:111623294
|
T | C | 8 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1181-460T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623294 | ||||||
| chr3:111623348
|
A | G | 2 | a0001c0001t0002g0035a0001c0011t0026g0036 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1181-406A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623348 | ||||||
| chr3:111623460
|
G | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-294G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623460 | ||||||
| chr3:111623707
|
C | T | 1 | a0002c0002t0002g0025 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1181-47C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623707 | ||||||
| chr3:111623733
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1181-21G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623733 | ||||||
| chr3:111623952
|
G | A | 3 | a0001c0001t0010g0019a0001c0001t0010g0046a0001c0001t0010g0099 | 3 | HG02165.hp1 NA19077.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1249+130G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 9/13 | chr3 | 111623952 | ||||||
| chr3:111623958
|
G | T | 1 | a0001c0001t0001g0226 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1249+136G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 9/13 | chr3 | 111623958 | ||||||
| chr3:111624056
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1249+234G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 9/13 | chr3 | 111624056 | ||||||
| chr3:111624187
|
G | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1250-146G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 9/13 | chr3 | 111624187 | ||||||
| chr3:111624222
|
C | T | 48 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0053others(45): Show | 49 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1250-111C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 9/13 | chr3 | 111624222 | ||||||
| chr3:111624446
|
G | T | 1 | a0001c0001t0019g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1321+42G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624446 | ||||||
| chr3:111624472
|
C | T | 11 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(8): Show | 11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321+68C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624472 | ||||||
| chr3:111624522
|
A | G | 1 | a0001c0001t0019g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1321+118A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624522 | ||||||
| chr3:111624729
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1321+325C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624729 | ||||||
| chr3:111624733
|
TGAGCAAT others(6): Show |
T | 2 | a0001c0001t0002g0035a0001c0011t0026g0036 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1321+330_1321+342d others(15): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624733 | ||||||
| chr3:111624753
|
C | A | 1 | a0001c0001t0004g0181 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1321+349C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624753 | ||||||
| chr3:111624837
|
G | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0103a0001c0001t0001g0118others(1): Show | 4 | NA18952.hp2 NA18961.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1321+433G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624837 | ||||||
| chr3:111624853
|
T | G | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+449T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624853 | ||||||
| chr3:111624899
|
A | G | 1 | a0001c0001t0019g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1321+495A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624899 | ||||||
| chr3:111624909
|
A | G | 90 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(87): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1321+505A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624909 | ||||||
| chr3:111625072
|
T | C | 90 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(87): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1321+668T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625072 | ||||||
| chr3:111625084
|
C | T | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1321+680C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625084 | ||||||
| chr3:111625167
|
C | T | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+763C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625167 | ||||||
| chr3:111625414
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1321+1010C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625414 | ||||||
| chr3:111625425
|
A | G | 11 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(8): Show | 11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321+1021A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625425 | ||||||
| chr3:111625426
|
T | C | 2 | a0001c0001t0002g0035a0001c0011t0026g0036 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1321+1022T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625426 | ||||||
| chr3:111625573
|
GA | G | 4 | a0001c0001t0001g0195a0001c0001t0022g0044a0001c0001t0023g0057others(1): Show | 4 | HG02055.hp2 HG02451.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1321+1177delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111625573 | |||||
| chr3:111625606
|
A | C | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+1202A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625606 | ||||||
| chr3:111626042
|
G | A | 11 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(8): Show | 11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321+1638G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626042 | ||||||
| chr3:111626161
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1321+1757C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626161 | ||||||
| chr3:111626168
|
G | T | 11 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(8): Show | 11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321+1764G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626168 | ||||||
| chr3:111626185
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(63): Show | 72 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1321+1781C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626185 | ||||||
| chr3:111626194
|
G | A | 11 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(8): Show | 11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321+1790G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626194 | ||||||
| chr3:111626206
|
C | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+1802C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626206 | ||||||
| chr3:111626306
|
C | CA | 124 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0037others(121): Show | 128 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1321+1924dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111626306 | |||||
| chr3:111626306
|
C | CAA | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.1321+1923_1321+192 others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111626306 | |||||
| chr3:111626353
|
C | A | 1 | a0001c0001t0002g0078 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1321+1949C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626353 | ||||||
| chr3:111626514
|
T | A | 3 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0002g0142 | 3 | NA18975.hp2 NA18981.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1321+2110T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626514 | ||||||
| chr3:111626516
|
C | T | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1321+2112C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626516 | ||||||
| chr3:111626525
|
T | G | 1 | a0002c0002t0002g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1321+2121T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626525 | ||||||
| chr3:111626718
|
A | T | 7 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0003g0148others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1321+2314A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626718 | ||||||
| chr3:111626782
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1321+2378C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626782 | ||||||
| chr3:111626959
|
G | A | 15 | a0001c0001t0001g0045a0001c0001t0004g0144a0001c0001t0004g0145others(12): Show | 15 | HG00735.hp1 HG01099.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1321+2555G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626959 | ||||||
| chr3:111627150
|
G | A | 90 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(87): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1321+2746G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627150 | ||||||
| chr3:111627236
|
T | C | 1 | a0001c0001t0001g0010 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1321+2832T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627236 | ||||||
| chr3:111627398
|
C | T | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+2994C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627398 | ||||||
| chr3:111627459
|
C | A | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321+3055C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627459 | ||||||
| chr3:111627470
|
C | T | 88 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0079others(85): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1321+3066C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627470 | ||||||
| chr3:111627913
|
A | G | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+3509A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627913 | ||||||
| chr3:111627936
|
G | A | 7 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0003g0148others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1321+3532G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627936 | ||||||
| chr3:111627961
|
A | G | 1 | a0001c0001t0006g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1321+3557A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627961 | ||||||
| chr3:111627994
|
G | A | 8 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1321+3590G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627994 | ||||||
| chr3:111628070
|
T | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+3666T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111628070 | ||||||
| chr3:111628344
|
T | C | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+3940T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111628344 | ||||||
| chr3:111628363
|
A | G | 1 | a0001c0001t0004g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1321+3959A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111628363 | ||||||
| chr3:111628710
|
G | A | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1321+4306G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111628710 | ||||||
| chr3:111628830
|
C | T | 83 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(80): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1321+4426C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111628830 | ||||||
| chr3:111628995
|
G | C | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+4591G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111628995 | ||||||
| chr3:111629044
|
T | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(273): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1321+4640T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629044 | ||||||
| chr3:111629172
|
T | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(273): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1321+4768T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629172 | ||||||
| chr3:111629689
|
T | A | 1 | a0001c0001t0004g0145 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1321+5285T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629689 | ||||||
| chr3:111629695
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1321+5291A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629695 | ||||||
| chr3:111629786
|
A | C | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1321+5382A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629786 | ||||||
| chr3:111629845
|
C | A | 1 | a0001c0001t0002g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1321+5441C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629845 | ||||||
| chr3:111629968
|
A | G | 1 | a0001c0001t0020g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1321+5564A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629968 | ||||||
| chr3:111630059
|
T | C | 1 | a0001c0011t0026g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1321+5655T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630059 | ||||||
| chr3:111630235
|
A | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0103a0001c0001t0001g0118others(1): Show | 4 | NA18952.hp2 NA18961.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1321+5831A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630235 | ||||||
| chr3:111630247
|
A | G | 7 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0003g0148others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1321+5843A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630247 | ||||||
| chr3:111630288
|
G | A | 8 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1321+5884G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630288 | ||||||
| chr3:111630354
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1321+5950C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630354 | ||||||
| chr3:111630359
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1321+5955G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630359 | ||||||
| chr3:111630480
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1321+6076G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630480 | ||||||
| chr3:111630547
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1321+6143A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630547 | ||||||
| chr3:111630674
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1321+6270C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630674 | ||||||
| chr3:111631266
|
A | AG | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-5930_1322-592 others(5): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111631266 | ||||||
| chr3:111631276
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1322-5920C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111631276 | ||||||
| chr3:111631333
|
G | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-5863G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111631333 | ||||||
| chr3:111631341
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1322-5855A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111631341 | ||||||
| chr3:111631630
|
G | GA | 7 | a0001c0001t0001g0091a0001c0001t0005g0190a0001c0001t0005g0192others(4): Show | 7 | HG01081.hp1 HG02896.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1322-5554dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111631630 | |||||
| chr3:111631630
|
GA | G | 54 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0053others(51): Show | 55 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1322-5554delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111631630 | |||||
| chr3:111631676
|
C | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-5520C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111631676 | ||||||
| chr3:111631804
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1322-5392A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111631804 | ||||||
| chr3:111632177
|
A | G | 51 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0041others(48): Show | 52 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1322-5019A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111632177 | ||||||
| chr3:111632191
|
G | T | 1 | a0001c0001t0012g0008 | 2 | HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1322-5005G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111632191 | ||||||
| chr3:111632648
|
A | G | 1 | a0001c0001t0009g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1322-4548A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111632648 | ||||||
| chr3:111632699
|
G | A | 1 | a0001c0001t0006g0185 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1322-4497G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111632699 | ||||||
| chr3:111632967
|
A | G | 2 | a0001c0001t0002g0035a0001c0011t0026g0036 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1322-4229A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111632967 | ||||||
| chr3:111633145
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1322-4051A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633145 | ||||||
| chr3:111633398
|
G | A | 1 | a0001c0001t0003g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1322-3798G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633398 | ||||||
| chr3:111633417
|
C | A | 6 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0003g0148others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1322-3779C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633417 | ||||||
| chr3:111633502
|
T | C | 1 | a0001c0005t0006g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1322-3694T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633502 | ||||||
| chr3:111633558
|
T | A | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1322-3638T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633558 | ||||||
| chr3:111633602
|
G | C | 1 | a0001c0011t0026g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1322-3594G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633602 | ||||||
| chr3:111633751
|
C | A | 1 | a0001c0001t0002g0055 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1322-3445C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633751 | ||||||
| chr3:111634221
|
A | C | 1 | a0007c0008t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1322-2975A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634221 | ||||||
| chr3:111634357
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1322-2839C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634357 | ||||||
| chr3:111634382
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1322-2814G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634382 | ||||||
| chr3:111634473
|
C | G | 1 | a0001c0001t0003g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1322-2723C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634473 | ||||||
| chr3:111634558
|
G | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-2638G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634558 | ||||||
| chr3:111634625
|
G | A | 86 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0079others(83): Show | 89 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1322-2571G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634625 | ||||||
| chr3:111634632
|
C | T | 2 | a0001c0001t0003g0074a0001c0001t0021g0061 | 2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1322-2564C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634632 | ||||||
| chr3:111634635
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1322-2561G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634635 | ||||||
| chr3:111634658
|
A | G | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-2538A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634658 | ||||||
| chr3:111634725
|
C | T | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-2471C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634725 | ||||||
| chr3:111634729
|
T | C | 1 | a0001c0001t0005g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1322-2467T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634729 | ||||||
| chr3:111634754
|
G | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-2442G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634754 | ||||||
| chr3:111634852
|
G | A | 49 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0053others(46): Show | 50 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1322-2344G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634852 | ||||||
| chr3:111634895
|
C | CA | 12 | a0001c0001t0002g0072a0001c0001t0005g0039a0001c0001t0005g0047others(9): Show | 12 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1322-2288dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111634895 | |||||
| chr3:111634895
|
CA | C | 15 | a0001c0001t0001g0045a0001c0001t0004g0144a0001c0001t0004g0145others(12): Show | 15 | HG00735.hp1 HG01099.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1322-2288delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111634895 | |||||
| chr3:111634972
|
G | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-2224G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634972 | ||||||
| chr3:111635002
|
C | T | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-2194C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635002 | ||||||
| chr3:111635339
|
T | C | 1 | a0002c0002t0006g0021 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1322-1857T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635339 | ||||||
| chr3:111635403
|
T | G | 7 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(4): Show | 8 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1322-1793T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635403 | ||||||
| chr3:111635404
|
A | T | 1 | a0001c0001t0020g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1322-1792A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635404 | ||||||
| chr3:111635617
|
A | C | 11 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(8): Show | 11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1322-1579A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635617 | ||||||
| chr3:111635769
|
G | A | 7 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0003g0148others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1322-1427G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635769 | ||||||
| chr3:111635788
|
T | C | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1322-1408T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635788 | ||||||
| chr3:111635933
|
G | A | 1 | a0001c0001t0006g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1322-1263G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635933 | ||||||
| chr3:111635986
|
C | G | 3 | a0001c0001t0002g0053a0001c0001t0002g0054a0002c0002t0002g0198 | 3 | HG02258.hp2 HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1322-1210C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635986 | ||||||
| chr3:111636109
|
C | T | 1 | a0002c0002t0001g0029 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1322-1087C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111636109 | ||||||
| chr3:111636206
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1322-990C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111636206 | ||||||
| chr3:111636392
|
C | A | 51 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0041others(48): Show | 52 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1322-804C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111636392 | ||||||
| chr3:111636394
|
T | C | 1 | a0001c0001t0025g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1322-802T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111636394 | ||||||
| chr3:111636574
|
A | C | 2 | a0001c0001t0006g0069a0001c0001t0006g0073 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1322-622A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111636574 | ||||||
| chr3:111636874
|
A | AT | 8 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1322-312dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111636874 | |||||
| chr3:111637431
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0122others(2): Show | 8 | HG02027.hp1 HG02074.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1387+170A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637431 | ||||||
| chr3:111637444
|
C | T | 1 | a0001c0001t0014g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1387+183C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637444 | ||||||
| chr3:111637527
|
A | G | 4 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387+266A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637527 | ||||||
| chr3:111637576
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1387+315T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637576 | ||||||
| chr3:111637577
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(269): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1387+316T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637577 | ||||||
| chr3:111637733
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0215a0001c0001t0001g0217 | 3 | HG02027.hp2 HG02523.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1388-346C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637733 | ||||||
| chr3:111637768
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1388-311A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637768 | ||||||
| chr3:111637795
|
CT | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1388-270delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 111637795 | |||||
| chr3:111637848
|
AT | A | 8 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1388-222delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 111637848 | |||||
| chr3:111637864
|
C | A | 90 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(87): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1388-215C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637864 | ||||||
| chr3:111638491
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1477+323G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638491 | ||||||
| chr3:111638528
|
C | G | 3 | a0001c0001t0002g0053a0001c0001t0002g0054a0002c0002t0002g0198 | 3 | HG02258.hp2 HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1477+360C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638528 | ||||||
| chr3:111638623
|
T | G | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1477+455T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638623 | ||||||
| chr3:111638660
|
A | G | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1477+492A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638660 | ||||||
| chr3:111638862
|
T | C | 8 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1477+694T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638862 | ||||||
| chr3:111638901
|
CA | C | 7 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0003g0148others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1477+738delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111638901 | |||||
| chr3:111638913
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1477+745T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638913 | ||||||
| chr3:111638997
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1477+829C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638997 | ||||||
| chr3:111639029
|
G | C | 8 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1477+861G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111639029 | ||||||
| chr3:111639283
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1477+1115G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111639283 | ||||||
| chr3:111639618
|
A | T | 1 | a0001c0001t0005g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1477+1450A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111639618 | ||||||
| chr3:111639815
|
GACAACCT others(6): Show |
G | 3 | a0001c0001t0001g0120a0002c0002t0001g0030a0002c0002t0001g0031 | 3 | NA18959.hp2 NA18974.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1477+1648_1477+166 others(17): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111639815 | ||||||
| chr3:111639935
|
G | A | 4 | a0001c0005t0006g0060a0001c0005t0006g0150a0001c0005t0006g0151others(1): Show | 4 | HG02622.hp1 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477+1767G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111639935 | ||||||
| chr3:111639995
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0253 | 2 | HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1477+1827G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111639995 | ||||||
| chr3:111640097
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1477+1929C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640097 | ||||||
| chr3:111640166
|
T | C | 1 | a0001c0004t0007g0238 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1477+1998T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640166 | ||||||
| chr3:111640185
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1477+2017A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640185 | ||||||
| chr3:111640264
|
C | G | 11 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(8): Show | 11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1477+2096C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640264 | ||||||
| chr3:111640486
|
A | G | 1 | a0001c0001t0003g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+2318A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640486 | ||||||
| chr3:111640501
|
C | G | 1 | a0001c0001t0004g0162 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1477+2333C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640501 | ||||||
| chr3:111640521
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0116 | 2 | HG00609.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1477+2353G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640521 | ||||||
| chr3:111640588
|
C | A | 1 | a0002c0002t0001g0030 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1477+2420C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640588 | ||||||
| chr3:111640633
|
A | G | 48 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0053others(45): Show | 49 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1477+2465A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640633 | ||||||
| chr3:111640817
|
G | C | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1477+2649G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640817 | ||||||
| chr3:111640854
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1477+2686A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640854 | ||||||
| chr3:111641469
|
C | T | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1477+3301C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111641469 | ||||||
| chr3:111641846
|
C | A | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG00735.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1477+3678C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111641846 | ||||||
| chr3:111642011
|
A | G | 51 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0041others(48): Show | 52 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1477+3843A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642011 | ||||||
| chr3:111642195
|
A | G | 1 | a0001c0001t0004g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1477+4027A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642195 | ||||||
| chr3:111642427
|
C | A | 1 | a0001c0001t0002g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1477+4259C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642427 | ||||||
| chr3:111642469
|
C | T | 1 | a0006c0010t0007g0222 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1477+4301C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642469 | ||||||
| chr3:111642561
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1477+4393C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642561 | ||||||
| chr3:111642584
|
G | A | 7 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0003g0148others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1477+4416G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642584 | ||||||
| chr3:111642607
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1477+4439G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642607 | ||||||
| chr3:111642611
|
C | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1477+4443C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642611 | ||||||
| chr3:111642636
|
G | A | 1 | a0002c0002t0001g0032 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1477+4468G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642636 | ||||||
| chr3:111642665
|
G | A | 4 | a0001c0001t0001g0259a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | NA18944.hp1 NA18948.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477+4497G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642665 | ||||||
| chr3:111642722
|
G | A | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1477+4554G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642722 | ||||||
| chr3:111642812
|
A | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(62): Show | 71 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.1477+4644A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642812 | ||||||
| chr3:111642816
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1477+4648T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642816 | ||||||
| chr3:111642927
|
A | AT | 90 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(87): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1478-4615dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111642927 | |||||
| chr3:111643070
|
T | TA | 13 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0241others(10): Show | 13 | HG00323.hp1 HG01261.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1478-4453dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111643070 | |||||
| chr3:111643070
|
TA | T | 9 | a0001c0001t0001g0037a0001c0001t0001g0127a0001c0001t0001g0176others(6): Show | 9 | HG01074.hp2 HG01167.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1478-4453delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111643070 | |||||
| chr3:111643084
|
A | C | 1 | a0001c0001t0001g0180 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1478-4459A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643084 | ||||||
| chr3:111643188
|
C | T | 5 | a0001c0001t0008g0009a0001c0001t0008g0143a0001c0001t0008g0264others(2): Show | 6 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478-4355C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643188 | ||||||
| chr3:111643218
|
T | A | 2 | a0001c0001t0002g0035a0001c0011t0026g0036 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1478-4325T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643218 | ||||||
| chr3:111643255
|
A | G | 1 | a0001c0001t0004g0163 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1478-4288A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643255 | ||||||
| chr3:111643268
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1478-4275A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643268 | ||||||
| chr3:111643293
|
T | G | 1 | a0001c0001t0004g0230 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1478-4250T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643293 | ||||||
| chr3:111643298
|
C | T | 1 | a0001c0001t0025g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1478-4245C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643298 | ||||||
| chr3:111643381
|
T | C | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1478-4162T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643381 | ||||||
| chr3:111643634
|
C | T | 1 | a0001c0001t0021g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1478-3909C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643634 | ||||||
| chr3:111643639
|
A | G | 1 | a0001c0001t0005g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1478-3904A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643639 | ||||||
| chr3:111643735
|
C | CA | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(162): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1478-3791dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111643735 | |||||
| chr3:111643735
|
C | CAA | 27 | a0001c0001t0001g0045a0001c0001t0001g0177a0001c0001t0001g0257others(24): Show | 28 | HG00735.hp1 HG01099.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1478-3792_1478-379 others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111643735 | |||||
| chr3:111643735
|
CA | C | 50 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0053others(47): Show | 51 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1478-3791delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111643735 | |||||
| chr3:111643931
|
A | C | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1478-3612A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643931 | ||||||
| chr3:111643961
|
T | G | 59 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0041others(56): Show | 61 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1478-3582T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643961 | ||||||
| chr3:111644172
|
T | C | 5 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1478-3371T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644172 | ||||||
| chr3:111644267
|
A | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0037others(9): Show | 12 | HG01081.hp1 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1478-3276A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644267 | ||||||
| chr3:111644463
|
C | A | 90 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(87): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1478-3080C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644463 | ||||||
| chr3:111644555
|
G | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1478-2988G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644555 | ||||||
| chr3:111644605
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1478-2938A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644605 | ||||||
| chr3:111644652
|
ACT | A | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1478-2889_1478-288 others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111644652 | |||||
| chr3:111644775
|
A | C | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1478-2768A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644775 | ||||||
| chr3:111644891
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 81 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1478-2652G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644891 | ||||||
| chr3:111645119
|
C | T | 1 | a0007c0008t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1478-2424C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645119 | ||||||
| chr3:111645120
|
A | G | 2 | a0001c0001t0002g0035a0001c0011t0026g0036 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1478-2423A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645120 | ||||||
| chr3:111645122
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1478-2421C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645122 | ||||||
| chr3:111645151
|
T | C | 7 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0003g0148others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1478-2392T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645151 | ||||||
| chr3:111645156
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1478-2387A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645156 | ||||||
| chr3:111645189
|
C | A | 80 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(77): Show | 82 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1478-2354C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645189 | ||||||
| chr3:111645210
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1478-2333C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645210 | ||||||
| chr3:111645350
|
A | G | 11 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0070others(8): Show | 11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1478-2193A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645350 | ||||||
| chr3:111645388
|
C | T | 2 | a0001c0001t0003g0074a0001c0001t0021g0061 | 2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1478-2155C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645388 | ||||||
| chr3:111645436
|
T | A | 90 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(87): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1478-2107T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645436 | ||||||
| chr3:111645524
|
A | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(285): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1478-2019A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645524 | ||||||
| chr3:111645572
|
C | G | 7 | a0001c0001t0004g0149a0001c0001t0004g0154a0001c0001t0004g0156others(4): Show | 7 | HG01099.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1478-1971C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645572 | ||||||
| chr3:111645812
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1478-1731G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645812 | ||||||
| chr3:111645824
|
C | A | 7 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0003g0148others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1478-1719C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645824 | ||||||
| chr3:111645849
|
A | G | 1 | a0002c0002t0002g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1478-1694A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645849 | ||||||
| chr3:111645921
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1478-1622A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645921 | ||||||
| chr3:111646097
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1478-1446C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111646097 | ||||||
| chr3:111646158
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1478-1385T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111646158 | ||||||
| chr3:111646321
|
A | G | 80 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(77): Show | 82 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1478-1222A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111646321 | ||||||
| chr3:111646370
|
C | T | 3 | a0001c0001t0005g0047a0001c0001t0005g0070a0001c0001t0005g0071 | 3 | HG01106.hp1 HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1478-1173C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111646370 | ||||||
| chr3:111646540
|
TA | T | 47 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0053others(44): Show | 48 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.1478-990delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111646540 | |||||
| chr3:111646829
|
A | G | 7 | a0001c0001t0007g0130a0001c0001t0007g0187a0001c0004t0007g0101others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1478-714A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111646829 | ||||||
| chr3:111646882
|
A | G | 90 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(87): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1478-661A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111646882 | ||||||
| chr3:111647038
|
A | G | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1478-505A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647038 | ||||||
| chr3:111647088
|
T | TA | 9 | a0001c0001t0001g0160a0001c0001t0001g0233a0001c0001t0002g0055others(6): Show | 9 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1478-434dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111647088 | |||||
| chr3:111647088
|
TA | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(110): Show | 120 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1478-434delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111647088 | |||||
| chr3:111647088
|
TAA | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0091a0001c0001t0001g0128others(3): Show | 6 | HG02165.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1478-435_1478-434d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111647088 | |||||
| chr3:111647100
|
A | C | 1 | a0001c0001t0002g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1478-443A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647100 | ||||||
| chr3:111647188
|
C | G | 9 | a0001c0001t0001g0115a0001c0001t0001g0160a0001c0001t0001g0216others(6): Show | 9 | HG00741.hp2 HG01258.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.1478-355C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647188 | ||||||
| chr3:111647207
|
A | G | 5 | a0001c0001t0001g0107a0001c0001t0001g0120a0001c0015t0001g0119others(2): Show | 5 | NA18939.hp2 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1478-336A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647207 | ||||||
| chr3:111647226
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0214 | 2 | HG01106.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1478-317A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647226 | ||||||
| chr3:111647319
|
T | C | 1 | a0001c0001t0003g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-224T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647319 | ||||||
| chr3:111647473
|
A | C | 1 | a0001c0011t0026g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1478-70A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647473 | ||||||
| chr3:111647709
|
A | G | 1 | a0008c0007t0002g0022 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1601+43A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111647709 | ||||||
| chr3:111647757
|
T | C | 1 | a0001c0001t0004g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1601+91T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111647757 | ||||||
| chr3:111647961
|
A | C | 14 | a0001c0001t0001g0045a0001c0001t0004g0144a0001c0001t0004g0145others(11): Show | 14 | HG00735.hp1 HG01099.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1601+295A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111647961 | ||||||
| chr3:111648092
|
CT | C | 83 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(80): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1601+433delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr3 | 111648092 | |||||
| chr3:111648243
|
C | A | 1 | a0001c0001t0002g0147 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1601+577C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648243 | ||||||
| chr3:111648302
|
C | T | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1601+636C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648302 | ||||||
| chr3:111648350
|
A | T | 12 | a0001c0001t0005g0039a0001c0001t0005g0047a0001c0001t0005g0062others(9): Show | 12 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1601+684A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648350 | ||||||
| chr3:111648374
|
A | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(281): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1601+708A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648374 | ||||||
| chr3:111648384
|
C | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1601+718C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648384 | ||||||
| chr3:111648485
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1601+819A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648485 | ||||||
| chr3:111648672
|
C | T | 90 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0035others(87): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1601+1006C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648672 | ||||||
| chr3:111648692
|
G | A | 1 | a0001c0003t0001g0193 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1602-1006G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648692 | ||||||
| chr3:111648723
|
G | C | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1602-975G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648723 | ||||||
| chr3:111648729
|
ATC | A | 4 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0013g0065others(1): Show | 4 | HG02055.hp1 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602-963_1602-962d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr3 | 111648729 | |||||
| chr3:111648803
|
G | A | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1602-895G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648803 | ||||||
| chr3:111648937
|
G | A | 1 | a0001c0001t0002g0140 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1602-761G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648937 | ||||||
| chr3:111648987
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1602-711C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648987 | ||||||
| chr3:111649130
|
T | C | 1 | a0002c0002t0001g0277 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1602-568T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111649130 | ||||||
| chr3:111649467
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1602-231A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111649467 | ||||||
| chr3:111649571
|
ACTGGGAG others(7): Show |
A | 3 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0109 | 5 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602-124_1602-111d others(16): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr3 | 111649571 | |||||
| chr3:111649572
|
CTGGGAGA others(5): Show |
C | 1 | a0001c0001t0001g0100 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1602-124_1602-113d others(14): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr3 | 111649572 | |||||
| chr3:111649604
|
T | G | 3 | a0001c0001t0022g0044a0001c0001t0023g0057a0001c0001t0024g0058 | 3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1602-94T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111649604 |