Search by Gene
| geneid | 10486 |
|---|---|
| ensemblid | ENSG00000112186.13 |
| hgncid | 20039 |
| symbol | CAP2 |
| name | cyclase associated actin cytoskeleton regulatory protein 2 |
| refseq_nuc | NM_006366.3 |
| refseq_prot | NP_006357.1 |
| ensembl_nuc | ENST00000229922.7 |
| ensembl_prot | ENSP00000229922.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 17393595 |
| end | 17557780 |
| strand | + |
| ver | v1.2 |
| region | chr6:17393595-17557780 |
| region5000 | chr6:17388595-17562780 |
| regionname0 | CAP2_chr6_17393595_17557780 |
| regionname5000 | CAP2_chr6_17388595_17562780 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 477 | 185 | 60 | 40 | 49 | 8 | 26 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0002 | 0/0 | 477 | 12 | 3 | 1 | 7 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0003 | 0/0 | 477 | 5 | 3 | 2 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0004 | 0/0 | 477 | 2 | 1 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0005 | 0/0 | 477 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0006 | 0/0 | 477 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1434 | 98 | 22 | 21 | 35 | 3 | 17 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0002 | 1/1 | 1434 | 62 | 20 | 17 | 9 | 5 | 9 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0003 | 0/0 | 1434 | 12 | 11 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0004 | 0/0 | 1434 | 6 | 2 | 1 | 3 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0005 | 0/0 | 1434 | 5 | 0 | 0 | 4 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0006 | 0/0 | 1434 | 5 | 0 | 0 | 5 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0007 | 0/0 | 1434 | 5 | 3 | 2 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0008 | 0/0 | 1434 | 3 | 3 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0009 | 0/0 | 1434 | 2 | 2 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0010 | 0/0 | 1434 | 2 | 1 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0011 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0012 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0013 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0014 | 0/0 | 1434 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0015 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| c0016 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1492 | 133 | 50 | 25 | 30 | 6 | 21 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| t0002 | 1/0 | 1491 | 67 | 15 | 18 | 24 | 2 | 7 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| t0003 | 0/0 | 1492 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| t0004 | 0/0 | 1492 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| t0005 | 0/0 | 1492 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| t0006 | 0/0 | 1492 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| t0007 | 0/0 | 1492 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| t0008 | 0/0 | 1492 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 0/0 | 98 | 22 | 21 | 35 | 3 | 17 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0002 | a0001 | c0002 | 1/1 | 62 | 20 | 17 | 9 | 5 | 9 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 12 | 11 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0009 | a0001 | c0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0011 | a0001 | c0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0013 | a0001 | c0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0014 | a0001 | c0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0002c0004 | a0002 | c0004 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0002c0005 | a0002 | c0005 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0002c0012 | a0002 | c0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0003c0007 | a0003 | c0007 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0004c0010 | a0004 | c0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0005c0015 | a0005 | c0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0006c0016 | a0006 | c0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 55 | 17 | 10 | 16 | 2 | 10 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 41 | 3 | 11 | 19 | 1 | 7 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/1 | 48 | 16 | 11 | 7 | 4 | 9 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0002t0002 | a0001 | c0002 | t0002 | 1/0 | 13 | 3 | 6 | 2 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0002t0006 | a0001 | c0002 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0003t0002 | a0001 | c0003 | t0002 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0008t0001 | a0001 | c0008 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0009t0001 | a0001 | c0009 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0011t0002 | a0001 | c0011 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0013t0001 | a0001 | c0013 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0001c0014t0008 | a0001 | c0014 | t0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0002c0004t0001 | a0002 | c0004 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0002c0004t0002 | a0002 | c0004 | t0002 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0002c0005t0001 | a0002 | c0005 | t0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0002c0005t0003 | a0002 | c0005 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0002c0005t0004 | a0002 | c0005 | t0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0002c0012t0001 | a0002 | c0012 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0003c0007t0001 | a0003 | c0007 | t0001 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0004c0010t0001 | a0004 | c0010 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0004c0010t0002 | a0004 | c0010 | t0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0005c0015t0001 | a0005 | c0015 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| a0006c0016t0001 | a0006 | c0016 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0010 | a0001 | c0001 | t0002 | g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0021 | a0001 | c0001 | t0002 | g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0023 | a0001 | c0001 | t0002 | g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0026 | a0001 | c0001 | t0002 | g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0027 | a0001 | c0001 | t0002 | g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0030 | a0001 | c0001 | t0002 | g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0031 | a0001 | c0001 | t0002 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0037 | a0001 | c0001 | t0002 | g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0042 | a0001 | c0001 | t0002 | g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0043 | a0001 | c0001 | t0002 | g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0045 | a0001 | c0001 | t0002 | g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0046 | a0001 | c0001 | t0002 | g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0049 | a0001 | c0001 | t0002 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0050 | a0001 | c0001 | t0002 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0055 | a0001 | c0001 | t0002 | g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0096 | a0001 | c0001 | t0002 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0102 | a0001 | c0001 | t0002 | g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0105 | a0001 | c0001 | t0002 | g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0121 | a0001 | c0001 | t0002 | g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0122 | a0001 | c0001 | t0002 | g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0126 | a0001 | c0001 | t0002 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0137 | a0001 | c0001 | t0002 | g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0141 | a0001 | c0001 | t0002 | g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0147 | a0001 | c0001 | t0002 | g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0148 | a0001 | c0001 | t0002 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0150 | a0001 | c0001 | t0002 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0152 | a0001 | c0001 | t0002 | g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0157 | a0001 | c0001 | t0002 | g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0158 | a0001 | c0001 | t0002 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0162 | a0001 | c0001 | t0002 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0163 | a0001 | c0001 | t0002 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0168 | a0001 | c0001 | t0002 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0169 | a0001 | c0001 | t0002 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0171 | a0001 | c0001 | t0002 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0172 | a0001 | c0001 | t0002 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0175 | a0001 | c0001 | t0002 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0176 | a0001 | c0001 | t0002 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0177 | a0001 | c0001 | t0002 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0181 | a0001 | c0001 | t0002 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0199 | a0001 | c0001 | t0002 | g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0002g0206 | a0001 | c0001 | t0002 | g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0005g0200 | a0001 | c0001 | t0005 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0001t0007g0201 | a0001 | c0001 | t0007 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0002 | a0001 | c0002 | t0001 | g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0005 | a0001 | c0002 | t0001 | g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0006 | a0001 | c0002 | t0001 | g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0011 | a0001 | c0002 | t0001 | g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0019 | a0001 | c0002 | t0001 | g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0035 | a0001 | c0002 | t0001 | g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0056 | a0001 | c0002 | t0001 | g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0058 | a0001 | c0002 | t0001 | g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0062 | a0001 | c0002 | t0001 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0071 | a0001 | c0002 | t0001 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0072 | a0001 | c0002 | t0001 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0090 | a0001 | c0002 | t0001 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0093 | a0001 | c0002 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0094 | a0001 | c0002 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0098 | a0001 | c0002 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0100 | a0001 | c0002 | t0001 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0101 | a0001 | c0002 | t0001 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0106 | a0001 | c0002 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0107 | a0001 | c0002 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0108 | a0001 | c0002 | t0001 | g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0109 | a0001 | c0002 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0112 | a0001 | c0002 | t0001 | g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0125 | a0001 | c0002 | t0001 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0128 | a0001 | c0002 | t0001 | g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0130 | a0001 | c0002 | t0001 | g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0132 | a0001 | c0002 | t0001 | g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0134 | a0001 | c0002 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0136 | a0001 | c0002 | t0001 | g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0138 | a0001 | c0002 | t0001 | g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0144 | a0001 | c0002 | t0001 | g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0145 | a0001 | c0002 | t0001 | g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0146 | a0001 | c0002 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0153 | a0001 | c0002 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0161 | a0001 | c0002 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0164 | a0001 | c0002 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0166 | a0001 | c0002 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0173 | a0001 | c0002 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0183 | a0001 | c0002 | t0001 | g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0184 | a0001 | c0002 | t0001 | g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0187 | a0001 | c0002 | t0001 | g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0188 | a0001 | c0002 | t0001 | g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0189 | a0001 | c0002 | t0001 | g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0190 | a0001 | c0002 | t0001 | g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0191 | a0001 | c0002 | t0001 | g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0192 | a0001 | c0002 | t0001 | g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0193 | a0001 | c0002 | t0001 | g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0197 | a0001 | c0002 | t0001 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0001g0198 | a0001 | c0002 | t0001 | g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0002g0073 | a0001 | c0002 | t0002 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0002g0111 | a0001 | c0002 | t0002 | g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0002g0113 | a0001 | c0002 | t0002 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0002g0114 | a0001 | c0002 | t0002 | g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0002g0115 | a0001 | c0002 | t0002 | g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0002g0116 | a0001 | c0002 | t0002 | g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0002g0117 | a0001 | c0002 | t0002 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0002g0118 | a0001 | c0002 | t0002 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0002g0129 | a0001 | c0002 | t0002 | g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0002g0135 | a0001 | c0002 | t0002 | g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0002g0139 | a0001 | c0002 | t0002 | g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0002g0160 | a0001 | c0002 | t0002 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0002g0167 | a0001 | c0002 | t0002 | g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0002t0006g0133 | a0001 | c0002 | t0006 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0003t0001g0038 | a0001 | c0003 | t0001 | g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0003t0001g0065 | a0001 | c0003 | t0001 | g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0003t0001g0082 | a0001 | c0003 | t0001 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0003t0001g0084 | a0001 | c0003 | t0001 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0003t0001g0088 | a0001 | c0003 | t0001 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0003t0001g0091 | a0001 | c0003 | t0001 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0003t0002g0047 | a0001 | c0003 | t0002 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0003t0002g0060 | a0001 | c0003 | t0002 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0003t0002g0064 | a0001 | c0003 | t0002 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0003t0002g0080 | a0001 | c0003 | t0002 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0003t0002g0087 | a0001 | c0003 | t0002 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0003t0002g0131 | a0001 | c0003 | t0002 | g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0006t0001g0017 | a0001 | c0006 | t0001 | g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0006t0001g0033 | a0001 | c0006 | t0001 | g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0006t0001g0120 | a0001 | c0006 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0006t0001g0149 | a0001 | c0006 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0006t0001g0155 | a0001 | c0006 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0008t0001g0051 | a0001 | c0008 | t0001 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0008t0001g0057 | a0001 | c0008 | t0001 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0008t0001g0204 | a0001 | c0008 | t0001 | g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0009t0001g0012 | a0001 | c0009 | t0001 | g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0009t0001g0014 | a0001 | c0009 | t0001 | g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0011t0002g0081 | a0001 | c0011 | t0002 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0013t0001g0092 | a0001 | c0013 | t0001 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0001c0014t0008g0015 | a0001 | c0014 | t0008 | g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0002c0004t0001g0089 | a0002 | c0004 | t0001 | g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0002c0004t0002g0077 | a0002 | c0004 | t0002 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0002c0004t0002g0079 | a0002 | c0004 | t0002 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0002c0004t0002g0097 | a0002 | c0004 | t0002 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0002c0004t0002g0156 | a0002 | c0004 | t0002 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0002c0004t0002g0182 | a0002 | c0004 | t0002 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0002c0005t0001g0003 | a0002 | c0005 | t0001 | g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0002c0005t0001g0104 | a0002 | c0005 | t0001 | g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0002c0005t0001g0203 | a0002 | c0005 | t0001 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0002c0005t0003g0170 | a0002 | c0005 | t0003 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0002c0005t0004g0024 | a0002 | c0005 | t0004 | g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0002c0012t0001g0013 | a0002 | c0012 | t0001 | g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0003c0007t0001g0059 | a0003 | c0007 | t0001 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0003c0007t0001g0066 | a0003 | c0007 | t0001 | g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0003c0007t0001g0110 | a0003 | c0007 | t0001 | g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0003c0007t0001g0119 | a0003 | c0007 | t0001 | g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0003c0007t0001g0205 | a0003 | c0007 | t0001 | g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0004c0010t0001g0063 | a0004 | c0010 | t0001 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0004c0010t0002g0061 | a0004 | c0010 | t0002 | g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0005c0015t0001g0070 | a0005 | c0015 | t0001 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 |
| a0006c0016t0001g0194 | a0006 | c0016 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0107 | EUR | GBR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | CAP2_chr6_17388595_17562780 | CAP2 |
| HG00438 | hp2 | a0001 | c0006 | t0001 | g0149 | EAS | CHS | CAP2_chr6_17388595_17562780 | CAP2 |
| HG00597 | hp1 | a0002 | c0004 | t0002 | g0156 | EAS | CHS | CAP2_chr6_17388595_17562780 | CAP2 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | CAP2_chr6_17388595_17562780 | CAP2 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | CHS | CAP2_chr6_17388595_17562780 | CAP2 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | CHS | CAP2_chr6_17388595_17562780 | CAP2 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG00735 | hp2 | a0002 | c0004 | t0001 | g0089 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0187 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01106 | hp2 | a0003 | c0007 | t0001 | g0110 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0129 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01243 | hp2 | a0003 | c0007 | t0001 | g0119 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01255 | hp1 | a0004 | c0010 | t0002 | g0061 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01361 | hp2 | a0001 | c0014 | t0008 | g0015 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0065 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0152 | EUR | IBS | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0191 | EUR | IBS | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0167 | EUR | IBS | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0192 | EUR | IBS | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01884 | hp2 | a0002 | c0012 | t0001 | g0013 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0201 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0114 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0115 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0111 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0135 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0116 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02055 | hp1 | a0001 | c0013 | t0001 | g0092 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02055 | hp2 | a0001 | c0008 | t0001 | g0204 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02135 | hp1 | a0001 | c0006 | t0001 | g0155 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02135 | hp2 | a0002 | c0005 | t0001 | g0003 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02280 | hp2 | a0003 | c0007 | t0001 | g0059 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0108 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0073 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02622 | hp1 | a0005 | c0015 | t0001 | g0070 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0145 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02717 | hp2 | a0002 | c0004 | t0002 | g0079 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02886 | hp2 | a0001 | c0002 | t0006 | g0133 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0072 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02897 | hp2 | a0004 | c0010 | t0001 | g0063 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0188 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02970 | hp1 | a0001 | c0003 | t0002 | g0064 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02976 | hp2 | a0002 | c0004 | t0002 | g0077 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03017 | hp2 | a0002 | c0005 | t0001 | g0104 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0047 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0060 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0144 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0084 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0189 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0131 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0093 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03453 | hp1 | a0001 | c0011 | t0002 | g0081 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03453 | hp2 | a0003 | c0007 | t0001 | g0066 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0106 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03540 | hp1 | a0003 | c0007 | t0001 | g0205 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03540 | hp2 | a0001 | c0009 | t0001 | g0014 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0082 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03579 | hp2 | a0001 | c0008 | t0001 | g0057 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03831 | hp2 | a0006 | c0016 | t0001 | g0194 | SAS | BEB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | BEB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0094 | SAS | BEB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | STU | CAP2_chr6_17388595_17562780 | CAP2 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | CAP2_chr6_17388595_17562780 | CAP2 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0056 | SAS | STU | CAP2_chr6_17388595_17562780 | CAP2 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | YRI | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0088 | AFR | YRI | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | CHB | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | CHB | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | CHB | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | YRI | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18990 | hp1 | a0001 | c0006 | t0001 | g0120 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18990 | hp2 | a0001 | c0006 | t0001 | g0033 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18995 | hp1 | a0002 | c0005 | t0003 | g0170 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA18999 | hp2 | a0001 | c0006 | t0001 | g0017 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19002 | hp2 | a0002 | c0004 | t0002 | g0097 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19003 | hp1 | a0002 | c0005 | t0001 | g0203 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19006 | hp2 | a0002 | c0005 | t0004 | g0024 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19043 | hp1 | a0001 | c0009 | t0001 | g0012 | AFR | LWK | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19057 | hp1 | a0002 | c0004 | t0002 | g0182 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0118 | AFR | ASW | CAP2_chr6_17388595_17562780 | CAP2 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0113 | AFR | ASW | CAP2_chr6_17388595_17562780 | CAP2 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0193 | EUR | TSI | CAP2_chr6_17388595_17562780 | CAP2 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02109 | hp1 | a0001 | c0003 | t0002 | g0087 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02486 | hp1 | a0001 | c0008 | t0001 | g0051 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0091 | AFR | LWK | CAP2_chr6_17388595_17562780 | CAP2 |
| NA21309 | hp2 | a0001 | c0003 | t0002 | g0080 | AFR | LWK | CAP2_chr6_17388595_17562780 | CAP2 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0183 | REF | REF | CAP2_chr6_17388595_17562780 | CAP2 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0139 | REF | REF | CAP2_chr6_17388595_17562780 | CAP2 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:17513875
|
A | C | 1 | a0006 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.557A>C | p.Lys186Thr | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/13 | 710/2925 | 557/1434 | 186/477 | chr6 | 17513875 | ||
| chr6:17513932
|
C | T | 1 | a0005 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.614C>T | p.Thr205Met | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/13 | 767/2925 | 614/1434 | 205/477 | chr6 | 17513932 | ||
| chr6:17541074
|
C | A | 1 | a0002 | 12 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(9): Show |
missense_variant | MODERATE | c.928C>A | p.Pro310Thr | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/13 | 1081/2925 | 928/1434 | 310/477 | chr6 | 17541074 | ||
| chr6:17541077
|
A | G | 1 | a0004 | 2 | HG01255.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.931A>G | p.Thr311Ala | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/13 | 1084/2925 | 931/1434 | 311/477 | chr6 | 17541077 | ||
| chr6:17541093
|
A | G | 1 | a0003 | 5 | HG01106.hp2 HG01243.hp2 HG02280.hp2 others(2): Show |
missense_variant | MODERATE | c.947A>G | p.Tyr316Cys | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/13 | 1100/2925 | 947/1434 | 316/477 | chr6 | 17541093 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:17421615
|
G | A | 1 | a0001c0011 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.60G>A | p.Ser20Ser | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/13 | 213/2925 | 60/1434 | 20/477 | chr6 | 17421615 | ||
| chr6:17426615
|
T | C | 5 | a0001c0008a0001c0009a0001c0013others(2): Show | 8 | HG01361.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
synonymous_variant | LOW | c.147T>C | p.Phe49Phe | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/13 | 300/2925 | 147/1434 | 49/477 | chr6 | 17426615 | ||
| chr6:17542956
|
A | C | 3 | a0001c0003a0001c0014a0005c0015 | 14 | HG01361.hp2 HG01496.hp2 HG02109.hp1 others(11): Show |
synonymous_variant | LOW | c.1122A>C | p.Ile374Ile | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 10/13 | 1275/2925 | 1122/1434 | 374/477 | chr6 | 17542956 | ||
| chr6:17543071
|
A | G | 13 | a0001c0001a0001c0003a0001c0006others(10): Show | 140 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(137): Show |
synonymous_variant | LOW | c.1137A>G | p.Lys379Lys | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/13 | 1290/2925 | 1137/1434 | 379/477 | chr6 | 17543071 | ||
| chr6:17551550
|
C | T | 2 | a0001c0006a0002c0005 | 10 | HG00438.hp2 HG02135.hp1 HG02135.hp2 others(7): Show |
synonymous_variant | LOW | c.1296C>T | p.Ile432Ile | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/13 | 1449/2925 | 1296/1434 | 432/477 | chr6 | 17551550 | ||
| chr6:17556370
|
C | T | 1 | a0001c0013 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1362C>T | p.Pro454Pro | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 1515/2925 | 1362/1434 | 454/477 | chr6 | 17556370 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:17393710
|
G | C | 1 | a0002c0005t0003 | 1 | NA18995.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/13 | 27846 | chr6 | 17393710 | |||||
| chr6:17556470
|
T | C | 1 | a0002c0005t0004 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*28T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 28 | chr6 | 17556470 | |||||
| chr6:17556557
|
A | T | 1 | a0001c0014t0008 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 115 | chr6 | 17556557 | |||||
| chr6:17556925
|
T | C | 1 | a0001c0001t0005 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 483 | chr6 | 17556925 | |||||
| chr6:17556996
|
A | ATT | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(17): Show | 139 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*554_*555insTT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 555 | chr6 | 17556996 | |||||
| chr6:17557010
|
A | C | 1 | a0001c0001t0007 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*568A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 568 | chr6 | 17557010 | |||||
| chr6:17557171
|
AT | A | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(17): Show | 139 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*737delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 737 | INFO_REALIGN_3_PRIME | chr6 | 17557171 | ||||
| chr6:17557497
|
A | G | 1 | a0001c0002t0006 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1055A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 1055 | chr6 | 17557497 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:17393872
|
T | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+126T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17393872 | ||||||
| chr6:17393999
|
C | T | 4 | a0001c0001t0002g0206a0001c0008t0001g0204a0002c0005t0001g0203others(1): Show | 4 | HG01943.hp2 HG02055.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+253C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17393999 | ||||||
| chr6:17394135
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-2+389C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394135 | ||||||
| chr6:17394158
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-2+412T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394158 | ||||||
| chr6:17394162
|
G | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-2+416G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394162 | ||||||
| chr6:17394210
|
C | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+464C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394210 | ||||||
| chr6:17394537
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+791G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394537 | ||||||
| chr6:17394602
|
C | T | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2+856C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394602 | ||||||
| chr6:17394748
|
G | GATACAAC others(4): Show |
1 | a0001c0001t0002g0055 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-2+1002_-2+1003ins others(11): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394748 | ||||||
| chr6:17394750
|
G | C | 1 | a0001c0001t0002g0055 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-2+1004G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394750 | ||||||
| chr6:17394861
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+1115G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394861 | ||||||
| chr6:17394892
|
A | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+1146A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394892 | ||||||
| chr6:17395069
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(47): Show | 50 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2+1323G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395069 | ||||||
| chr6:17395239
|
A | G | 4 | a0001c0001t0001g0202a0001c0001t0002g0199a0001c0001t0005g0200others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+1493A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395239 | ||||||
| chr6:17395365
|
T | C | 1 | a0001c0002t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-2+1619T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395365 | ||||||
| chr6:17395426
|
A | C | 3 | a0001c0001t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02970.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2+1680A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395426 | ||||||
| chr6:17395505
|
G | A | 2 | a0001c0002t0001g0058a0001c0008t0001g0057 | 2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-2+1759G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395505 | ||||||
| chr6:17395581
|
A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+1835A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395581 | ||||||
| chr6:17395626
|
C | A | 28 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(25): Show | 28 | HG01167.hp2 HG01255.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.-2+1880C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395626 | ||||||
| chr6:17395701
|
T | C | 2 | a0001c0001t0001g0001a0001c0002t0001g0002 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-2+1955T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395701 | ||||||
| chr6:17395702
|
T | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(93): Show |
intron_variant | MODIFIER | c.-2+1956T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395702 | ||||||
| chr6:17395761
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+2015C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395761 | ||||||
| chr6:17395791
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+2045G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395791 | ||||||
| chr6:17395889
|
T | G | 2 | a0001c0001t0001g0196a0001c0002t0001g0197 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2+2143T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395889 | ||||||
| chr6:17396208
|
T | C | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0002t0001g0062others(7): Show | 10 | HG01255.hp1 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+2462T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17396208 | ||||||
| chr6:17396291
|
T | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+2545T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17396291 | ||||||
| chr6:17396424
|
A | G | 3 | a0001c0001t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02970.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2+2678A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17396424 | ||||||
| chr6:17396556
|
G | C | 2 | a0001c0002t0001g0093a0001c0002t0001g0094 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-2+2810G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17396556 | ||||||
| chr6:17396749
|
C | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+3003C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17396749 | ||||||
| chr6:17396885
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(95): Show |
intron_variant | MODIFIER | c.-2+3139T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17396885 | ||||||
| chr6:17397100
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+3354C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397100 | ||||||
| chr6:17397203
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(52): Show | 55 | HG00099.hp1 HG01106.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.-2+3457A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397203 | ||||||
| chr6:17397205
|
G | A | 3 | a0001c0001t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02970.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2+3459G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397205 | ||||||
| chr6:17397207
|
G | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+3461G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397207 | ||||||
| chr6:17397306
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+3560G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397306 | ||||||
| chr6:17397349
|
C | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+3603C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397349 | ||||||
| chr6:17397432
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+3686C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397432 | ||||||
| chr6:17397466
|
G | A | 4 | a0001c0001t0001g0202a0001c0001t0002g0199a0001c0001t0005g0200others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+3720G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397466 | ||||||
| chr6:17397588
|
G | C | 4 | a0001c0001t0001g0095a0001c0001t0002g0096a0001c0002t0001g0098others(1): Show | 4 | HG00438.hp1 HG00597.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+3842G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397588 | ||||||
| chr6:17397596
|
G | A | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-2+3850G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397596 | ||||||
| chr6:17397694
|
C | CA | 68 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(65): Show | 68 | HG00099.hp2 HG01071.hp1 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.-2+3971dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17397694 | |||||
| chr6:17397694
|
C | CAA | 15 | a0001c0001t0001g0069a0001c0001t0001g0103a0001c0001t0001g0196others(12): Show | 15 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2+3970_-2+3971dup others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17397694 | |||||
| chr6:17397694
|
CAAAAAAA others(4): Show |
C | 8 | a0001c0002t0001g0056a0001c0002t0001g0188a0001c0002t0001g0189others(5): Show | 8 | HG00741.hp2 HG01516.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2+3961_-2+3971del others(11): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17397694 | |||||
| chr6:17397720
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-2+3974A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397720 | ||||||
| chr6:17397800
|
G | A | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0002t0001g0062others(7): Show | 10 | HG01255.hp1 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+4054G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397800 | ||||||
| chr6:17397924
|
G | A | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0002t0001g0062others(7): Show | 10 | HG01255.hp1 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+4178G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397924 | ||||||
| chr6:17397924
|
GA | G | 8 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0002t0001g0136others(5): Show | 8 | HG00642.hp2 HG00741.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+4191delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17397924 | |||||
| chr6:17397925
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-2+4179A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397925 | ||||||
| chr6:17398141
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-2+4395C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398141 | ||||||
| chr6:17398252
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(53): Show | 56 | HG00099.hp1 HG01106.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.-2+4506A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398252 | ||||||
| chr6:17398288
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-2+4542A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398288 | ||||||
| chr6:17398299
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.-2+4553A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398299 | ||||||
| chr6:17398519
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-2+4773G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398519 | ||||||
| chr6:17398528
|
C | CT | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(49): Show | 52 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.-2+4796dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17398528 | |||||
| chr6:17398563
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(38): Show | 41 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.-2+4817C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398563 | ||||||
| chr6:17398681
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0002g0042others(3): Show | 6 | HG00099.hp1 HG01175.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+4935C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398681 | ||||||
| chr6:17398814
|
G | A | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-2+5068G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398814 | ||||||
| chr6:17398954
|
T | G | 1 | a0001c0002t0001g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-2+5208T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398954 | ||||||
| chr6:17399122
|
G | A | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-2+5376G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17399122 | ||||||
| chr6:17399295
|
T | C | 1 | a0001c0003t0002g0060 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-2+5549T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17399295 | ||||||
| chr6:17399333
|
G | A | 28 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(25): Show | 28 | HG01167.hp2 HG01255.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.-2+5587G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17399333 | ||||||
| chr6:17399500
|
G | A | 6 | a0001c0002t0001g0090a0001c0003t0001g0088a0001c0003t0001g0091others(3): Show | 6 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+5754G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17399500 | ||||||
| chr6:17399505
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-2+5759A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17399505 | ||||||
| chr6:17399655
|
A | G | 2 | a0001c0001t0002g0181a0002c0004t0002g0182 | 2 | NA18939.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-2+5909A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17399655 | ||||||
| chr6:17400064
|
C | CA | 59 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(56): Show | 59 | HG00099.hp1 HG01106.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.-2+6330dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17400064 | |||||
| chr6:17400064
|
C | CAA | 7 | a0001c0002t0001g0090a0001c0003t0001g0088a0001c0003t0001g0091others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+6329_-2+6330dup others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17400064 | |||||
| chr6:17400104
|
T | C | 23 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0016others(20): Show | 23 | HG01192.hp1 HG02027.hp2 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+6358T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17400104 | ||||||
| chr6:17400141
|
G | A | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-2+6395G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17400141 | ||||||
| chr6:17400349
|
G | A | 14 | a0001c0001t0001g0202a0001c0001t0002g0010a0001c0001t0002g0049others(11): Show | 14 | HG01109.hp2 HG01361.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2+6603G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17400349 | ||||||
| chr6:17400408
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-2+6662T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17400408 | ||||||
| chr6:17400411
|
A | G | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-2+6665A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17400411 | ||||||
| chr6:17400758
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-2+7012G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17400758 | ||||||
| chr6:17400864
|
CA | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(92): Show | 95 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(92): Show |
intron_variant | MODIFIER | c.-2+7134delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17400864 | |||||
| chr6:17401193
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-2+7447G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17401193 | ||||||
| chr6:17401519
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-2+7773T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17401519 | ||||||
| chr6:17401568
|
T | G | 4 | a0001c0001t0001g0202a0001c0001t0002g0199a0001c0001t0005g0200others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+7822T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17401568 | ||||||
| chr6:17401600
|
G | A | 14 | a0001c0001t0001g0202a0001c0001t0002g0010a0001c0001t0002g0049others(11): Show | 14 | HG01109.hp2 HG01361.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2+7854G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17401600 | ||||||
| chr6:17402113
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-2+8367G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17402113 | ||||||
| chr6:17402250
|
C | T | 1 | a0001c0008t0001g0204 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-2+8504C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17402250 | ||||||
| chr6:17402358
|
CA | C | 3 | a0001c0001t0001g0127a0001c0002t0001g0128a0001c0002t0002g0129 | 3 | HG01071.hp1 HG01167.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-2+8618delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17402358 | |||||
| chr6:17402389
|
T | G | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-2+8643T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17402389 | ||||||
| chr6:17402490
|
G | C | 1 | a0001c0006t0001g0017 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-2+8744G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17402490 | ||||||
| chr6:17402668
|
G | C | 1 | a0001c0001t0002g0148 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-2+8922G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17402668 | ||||||
| chr6:17402786
|
C | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(95): Show |
intron_variant | MODIFIER | c.-2+9040C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17402786 | ||||||
| chr6:17403061
|
T | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(39): Show | 42 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.-2+9315T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403061 | ||||||
| chr6:17403370
|
G | T | 40 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(37): Show | 40 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.-2+9624G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403370 | ||||||
| chr6:17403471
|
A | G | 31 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(28): Show | 31 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-2+9725A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403471 | ||||||
| chr6:17403473
|
A | G | 4 | a0001c0003t0002g0060a0001c0003t0002g0064a0001c0003t0002g0087others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+9727A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403473 | ||||||
| chr6:17403602
|
T | A | 40 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(37): Show | 40 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.-2+9856T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403602 | ||||||
| chr6:17403716
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.-2+9970A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403716 | ||||||
| chr6:17403735
|
A | T | 3 | a0001c0003t0002g0060a0001c0003t0002g0064a0001c0003t0002g0087 | 3 | HG02109.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-2+9989A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403735 | ||||||
| chr6:17403934
|
G | T | 40 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(37): Show | 40 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.-2+10188G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403934 | ||||||
| chr6:17404333
|
C | T | 4 | a0001c0001t0001g0069a0001c0002t0001g0062a0004c0010t0001g0063others(1): Show | 4 | HG01255.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+10587C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404333 | ||||||
| chr6:17404370
|
C | T | 8 | a0001c0001t0001g0069a0001c0002t0001g0062a0001c0003t0002g0060others(5): Show | 8 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+10624C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404370 | ||||||
| chr6:17404408
|
A | G | 4 | a0001c0001t0002g0096a0001c0002t0001g0098a0001c0002t0001g0146others(1): Show | 4 | HG00597.hp2 HG00609.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+10662A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404408 | ||||||
| chr6:17404422
|
G | A | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-2+10676G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404422 | ||||||
| chr6:17404538
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-2+10792G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404538 | ||||||
| chr6:17404559
|
G | A | 32 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(29): Show | 32 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.-2+10813G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404559 | ||||||
| chr6:17404604
|
CA | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(55): Show | 58 | HG00099.hp1 HG00609.hp2 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.-2+10874delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17404604 | |||||
| chr6:17404727
|
C | T | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-2+10981C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404727 | ||||||
| chr6:17404770
|
C | CA | 15 | a0001c0001t0001g0018a0001c0001t0001g0202a0001c0001t0002g0010others(12): Show | 15 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2+11043dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17404770 | |||||
| chr6:17404814
|
C | T | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-2+11068C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404814 | ||||||
| chr6:17404917
|
A | C | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-2+11171A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404917 | ||||||
| chr6:17404918
|
C | A | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-2+11172C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404918 | ||||||
| chr6:17404919
|
C | A | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-2+11173C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404919 | ||||||
| chr6:17404947
|
T | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(53): Show | 56 | HG00099.hp1 HG00438.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.-2+11201T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404947 | ||||||
| chr6:17405018
|
C | G | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-2+11272C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405018 | ||||||
| chr6:17405051
|
T | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(86): Show | 89 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.-2+11305T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405051 | ||||||
| chr6:17405079
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-2+11333C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405079 | ||||||
| chr6:17405120
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(40): Show | 43 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.-2+11374C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405120 | ||||||
| chr6:17405267
|
A | G | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-2+11521A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405267 | ||||||
| chr6:17405275
|
G | A | 1 | a0001c0001t0002g0150 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-2+11529G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405275 | ||||||
| chr6:17405277
|
G | T | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-2+11531G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405277 | ||||||
| chr6:17405285
|
G | A | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-2+11539G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405285 | ||||||
| chr6:17405298
|
T | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(98): Show | 101 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(98): Show |
intron_variant | MODIFIER | c.-2+11552T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405298 | ||||||
| chr6:17405299
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(53): Show | 56 | HG00099.hp1 HG00438.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.-2+11553G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405299 | ||||||
| chr6:17405318
|
G | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(40): Show | 43 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.-2+11572G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405318 | ||||||
| chr6:17405360
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-2+11614C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405360 | ||||||
| chr6:17405368
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-2+11622T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405368 | ||||||
| chr6:17405498
|
G | GTC | 8 | a0001c0001t0001g0069a0001c0001t0001g0095a0001c0001t0001g0202others(5): Show | 8 | HG00438.hp1 HG01109.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+11783_-2+11784d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17405498 | |||||
| chr6:17405498
|
G | GTCTCTC | 6 | a0001c0002t0001g0062a0001c0003t0002g0060a0001c0003t0002g0064others(3): Show | 6 | HG01255.hp1 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+11779_-2+11784d others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17405498 | |||||
| chr6:17405498
|
GTCTC | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0195others(2): Show | 5 | HG01516.hp1 HG01952.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+11781_-2+11784d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17405498 | |||||
| chr6:17405498
|
GTCTCTCT others(1): Show |
G | 55 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(52): Show | 55 | HG00099.hp1 HG00438.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2+11777_-2+11784d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17405498 | |||||
| chr6:17405498
|
GTCTCTCT others(5): Show |
G | 30 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(27): Show | 30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-2+11773_-2+11784d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17405498 | |||||
| chr6:17405683
|
G | C | 4 | a0001c0001t0001g0179a0001c0006t0001g0149a0001c0008t0001g0051others(1): Show | 4 | HG00438.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+11937G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405683 | ||||||
| chr6:17405763
|
C | T | 30 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(27): Show | 30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-2+12017C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405763 | ||||||
| chr6:17405777
|
G | A | 4 | a0001c0003t0002g0060a0001c0003t0002g0064a0001c0003t0002g0087others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+12031G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405777 | ||||||
| chr6:17405784
|
A | C | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2+12038A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405784 | ||||||
| chr6:17405807
|
C | G | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-2+12061C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405807 | ||||||
| chr6:17405815
|
G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 86 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.-2+12069G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405815 | ||||||
| chr6:17405825
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-2+12079C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405825 | ||||||
| chr6:17405857
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(53): Show | 56 | HG00099.hp1 HG00438.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.-2+12111C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405857 | ||||||
| chr6:17405878
|
C | T | 30 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(27): Show | 30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-2+12132C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405878 | ||||||
| chr6:17405894
|
C | T | 4 | a0001c0002t0001g0090a0001c0003t0001g0088a0001c0003t0001g0091others(1): Show | 4 | HG00735.hp2 HG01243.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+12148C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405894 | ||||||
| chr6:17406128
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-2+12382C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406128 | ||||||
| chr6:17406145
|
C | G | 4 | a0001c0001t0001g0179a0001c0006t0001g0149a0001c0008t0001g0051others(1): Show | 4 | HG00438.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+12399C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406145 | ||||||
| chr6:17406372
|
A | G | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2+12626A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406372 | ||||||
| chr6:17406398
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0002g0049 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-2+12657_-2+12667d others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | |||||
| chr6:17406398
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0002g0010a0001c0002t0001g0011 | 2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-2+12656_-2+12667d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | |||||
| chr6:17406398
|
C | CTTTTTTT others(8): Show |
1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2+12653_-2+12667d others(17): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | |||||
| chr6:17406398
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0004 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-2+12667_-2+12668i others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | |||||
| chr6:17406398
|
C | CTTTTTTT others(10): Show |
15 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(12): Show | 15 | HG00099.hp1 HG01106.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(19): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | |||||
| chr6:17406398
|
C | CTTTTTTT others(11): Show |
19 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0018others(16): Show | 19 | HG01192.hp1 HG01361.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(20): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | |||||
| chr6:17406398
|
C | CTTTTTTT others(12): Show |
6 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0040others(3): Show | 6 | HG01175.hp2 HG02071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(21): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | |||||
| chr6:17406398
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0001g0041a0001c0006t0001g0033 | 2 | HG03209.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | |||||
| chr6:17406398
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0001g0179 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-2+12667_-2+12668i others(24): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | |||||
| chr6:17406398
|
C | CTTTTTTT others(16): Show |
5 | a0001c0006t0001g0149a0001c0008t0001g0204a0001c0009t0001g0012others(2): Show | 5 | HG00438.hp2 HG01361.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(25): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | |||||
| chr6:17406398
|
C | CTTTTTTT others(17): Show |
1 | a0001c0009t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-2+12667_-2+12668i others(26): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | |||||
| chr6:17406398
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2+12667_-2+12668i others(27): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | |||||
| chr6:17406412
|
T | TTTTTTTT others(14): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG01167.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(23): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406412 | |||||
| chr6:17406412
|
T | TTTTTTTT others(15): Show |
7 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0002t0001g0002others(4): Show | 7 | HG02258.hp1 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(24): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406412 | |||||
| chr6:17406412
|
T | TTTTTTTT others(16): Show |
10 | a0001c0002t0001g0197a0001c0002t0006g0133a0001c0003t0001g0065others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(25): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406412 | |||||
| chr6:17406412
|
T | TTTTTTTT others(17): Show |
8 | a0001c0001t0001g0067a0001c0001t0001g0083a0001c0001t0001g0085others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(26): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406412 | |||||
| chr6:17406412
|
T | TTTTTTTT others(18): Show |
3 | a0001c0001t0001g0068a0001c0001t0001g0086a0005c0015t0001g0070 | 3 | HG02622.hp1 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(27): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406412 | |||||
| chr6:17406454
|
T | G | 1 | a0001c0002t0001g0106 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-2+12708T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406454 | ||||||
| chr6:17406479
|
C | T | 11 | a0001c0001t0001g0069a0001c0001t0001g0202a0001c0001t0002g0199others(8): Show | 11 | HG01109.hp2 HG01255.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2+12733C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406479 | ||||||
| chr6:17406583
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(98): Show | 101 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(98): Show |
intron_variant | MODIFIER | c.-2+12837A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406583 | ||||||
| chr6:17406677
|
C | T | 13 | a0001c0001t0001g0179a0001c0001t0002g0010a0001c0001t0002g0049others(10): Show | 13 | HG00438.hp2 HG01361.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-2+12931C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406677 | ||||||
| chr6:17406771
|
C | T | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-2+13025C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406771 | ||||||
| chr6:17406795
|
A | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(40): Show | 43 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.-2+13049A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406795 | ||||||
| chr6:17406843
|
C | G | 4 | a0001c0003t0002g0060a0001c0003t0002g0064a0001c0003t0002g0087others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+13097C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406843 | ||||||
| chr6:17406925
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-2+13179G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406925 | ||||||
| chr6:17406942
|
A | C | 4 | a0001c0003t0002g0060a0001c0003t0002g0064a0001c0003t0002g0087others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+13196A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406942 | ||||||
| chr6:17407394
|
G | A | 4 | a0001c0001t0001g0179a0001c0002t0001g0198a0001c0006t0001g0149others(1): Show | 4 | HG00438.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+13648G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17407394 | ||||||
| chr6:17407479
|
G | GA | 10 | a0001c0001t0001g0179a0001c0001t0002g0010a0001c0001t0002g0026others(7): Show | 10 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+13747dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17407479 | |||||
| chr6:17407514
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-2+13768C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17407514 | ||||||
| chr6:17407563
|
G | T | 1 | a0001c0001t0001g0001 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2+13817G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17407563 | ||||||
| chr6:17407778
|
CA | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.-1-13753delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17407778 | |||||
| chr6:17407778
|
CAA | C | 10 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0002g0176others(7): Show | 10 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-13754_-1-13753d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17407778 | |||||
| chr6:17407778
|
CAAA | C | 29 | a0001c0001t0001g0067a0001c0001t0001g0074a0001c0001t0001g0075others(26): Show | 29 | HG00438.hp2 HG00735.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1-13755_-1-13753d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17407778 | |||||
| chr6:17408032
|
T | C | 1 | a0002c0004t0002g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-1-13523T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408032 | ||||||
| chr6:17408160
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(86): Show | 89 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.-1-13395G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408160 | ||||||
| chr6:17408272
|
C | T | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-1-13283C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408272 | ||||||
| chr6:17408273
|
G | A | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-13282G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408273 | ||||||
| chr6:17408275
|
C | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(41): Show | 44 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.-1-13280C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408275 | ||||||
| chr6:17408385
|
C | T | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-13170C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408385 | ||||||
| chr6:17408470
|
T | C | 33 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(30): Show | 33 | HG00438.hp2 HG00735.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1-13085T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408470 | ||||||
| chr6:17408551
|
C | T | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-13004C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408551 | ||||||
| chr6:17408567
|
G | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(40): Show | 43 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.-1-12988G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408567 | ||||||
| chr6:17408602
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(86): Show | 89 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.-1-12953G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408602 | ||||||
| chr6:17408660
|
C | CT | 25 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0083others(22): Show | 25 | HG00735.hp2 HG01243.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.-1-12876dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17408660 | |||||
| chr6:17408660
|
C | CTT | 60 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(57): Show | 60 | HG00099.hp1 HG01106.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-1-12877_-1-12876d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17408660 | |||||
| chr6:17408660
|
CT | C | 10 | a0001c0001t0001g0052a0001c0001t0001g0159a0001c0001t0002g0157others(7): Show | 10 | HG01891.hp2 HG01943.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-12876delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17408660 | |||||
| chr6:17408685
|
G | A | 30 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(27): Show | 30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-12870G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408685 | ||||||
| chr6:17408818
|
C | A | 6 | a0001c0001t0001g0202a0001c0001t0002g0199a0001c0001t0005g0200others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-12737C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408818 | ||||||
| chr6:17408818
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-1-12737C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408818 | ||||||
| chr6:17408836
|
A | AT | 8 | a0001c0001t0002g0010a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 8 | HG01361.hp2 HG01884.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-12713dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17408836 | |||||
| chr6:17408841
|
T | G | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-12714T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408841 | ||||||
| chr6:17408859
|
C | T | 3 | a0001c0001t0001g0179a0001c0006t0001g0149a0001c0008t0001g0204 | 3 | HG00438.hp2 HG02055.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.-1-12696C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408859 | ||||||
| chr6:17408862
|
G | T | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-12693G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408862 | ||||||
| chr6:17408904
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(50): Show | 53 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.-1-12651T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408904 | ||||||
| chr6:17408968
|
C | A | 1 | a0001c0001t0002g0199 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-1-12587C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408968 | ||||||
| chr6:17409025
|
T | C | 30 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(27): Show | 30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-12530T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409025 | ||||||
| chr6:17409035
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-1-12520G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409035 | ||||||
| chr6:17409109
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-12446C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409109 | ||||||
| chr6:17409241
|
A | G | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-12314A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409241 | ||||||
| chr6:17409264
|
C | T | 1 | a0002c0004t0002g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-1-12291C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409264 | ||||||
| chr6:17409265
|
G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(49): Show | 52 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.-1-12290G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409265 | ||||||
| chr6:17409294
|
C | T | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-12261C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409294 | ||||||
| chr6:17409334
|
T | C | 1 | a0001c0002t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-1-12221T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409334 | ||||||
| chr6:17409562
|
G | A | 33 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(30): Show | 33 | HG00438.hp2 HG00735.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1-11993G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409562 | ||||||
| chr6:17409747
|
G | A | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-11808G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409747 | ||||||
| chr6:17409882
|
G | C | 1 | a0001c0002t0001g0183 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-1-11673G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409882 | ||||||
| chr6:17409960
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-1-11595G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409960 | ||||||
| chr6:17409998
|
G | A | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-11557G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409998 | ||||||
| chr6:17410046
|
C | G | 1 | a0001c0008t0001g0204 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-1-11509C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410046 | ||||||
| chr6:17410113
|
C | G | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-11442C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410113 | ||||||
| chr6:17410142
|
T | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-1-11413T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410142 | ||||||
| chr6:17410440
|
T | A | 1 | a0001c0002t0001g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-1-11115T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410440 | ||||||
| chr6:17410537
|
C | T | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-11018C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410537 | ||||||
| chr6:17410572
|
AT | A | 5 | a0001c0001t0001g0004a0001c0001t0002g0206a0001c0002t0001g0005others(2): Show | 5 | HG01943.hp2 HG02486.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-10968delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17410572 | |||||
| chr6:17410597
|
T | TCTCGCTC others(6): Show |
1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-10957_-1-10956i others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17410597 | |||||
| chr6:17410626
|
C | T | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-10929C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410626 | ||||||
| chr6:17410658
|
C | T | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-10897C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410658 | ||||||
| chr6:17410701
|
G | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-1-10854G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410701 | ||||||
| chr6:17410703
|
G | A | 1 | a0001c0002t0001g0161 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-1-10852G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410703 | ||||||
| chr6:17410801
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(103): Show | 106 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(103): Show |
intron_variant | MODIFIER | c.-1-10754T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410801 | ||||||
| chr6:17410802
|
G | A | 2 | a0001c0008t0001g0051a0001c0013t0001g0092 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-1-10753G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410802 | ||||||
| chr6:17411046
|
TAC | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(51): Show | 54 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(51): Show |
intron_variant | MODIFIER | c.-1-10505_-1-10504d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17411046 | |||||
| chr6:17411133
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-1-10422C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411133 | ||||||
| chr6:17411354
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(92): Show | 95 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(92): Show |
intron_variant | MODIFIER | c.-1-10201C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411354 | ||||||
| chr6:17411483
|
A | C | 30 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(27): Show | 30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-10072A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411483 | ||||||
| chr6:17411555
|
C | T | 6 | a0001c0001t0001g0069a0001c0002t0001g0062a0001c0002t0001g0144others(3): Show | 6 | HG01255.hp1 HG02109.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-10000C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411555 | ||||||
| chr6:17411728
|
C | T | 2 | a0001c0001t0002g0126a0001c0001t0002g0175 | 2 | NA18747.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-1-9827C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411728 | ||||||
| chr6:17411798
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-1-9757C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411798 | ||||||
| chr6:17411799
|
G | C | 1 | a0001c0002t0001g0019 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-1-9756G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411799 | ||||||
| chr6:17411841
|
T | A | 30 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(27): Show | 30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-9714T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411841 | ||||||
| chr6:17411897
|
A | G | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-9658A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411897 | ||||||
| chr6:17412028
|
T | C | 30 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(27): Show | 30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-9527T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412028 | ||||||
| chr6:17412076
|
T | C | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-9479T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412076 | ||||||
| chr6:17412134
|
A | G | 30 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(27): Show | 30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-9421A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412134 | ||||||
| chr6:17412328
|
T | C | 30 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(27): Show | 30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-9227T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412328 | ||||||
| chr6:17412498
|
A | G | 30 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(27): Show | 30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-9057A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412498 | ||||||
| chr6:17412545
|
T | C | 5 | a0001c0001t0001g0202a0001c0001t0002g0199a0001c0001t0005g0200others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-9010T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412545 | ||||||
| chr6:17412954
|
A | G | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-8601A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412954 | ||||||
| chr6:17413055
|
G | T | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-1-8500G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413055 | ||||||
| chr6:17413062
|
A | G | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-8493A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413062 | ||||||
| chr6:17413114
|
C | A | 1 | a0001c0002t0001g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-1-8441C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413114 | ||||||
| chr6:17413149
|
A | C | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-8406A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413149 | ||||||
| chr6:17413332
|
T | C | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-8223T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413332 | ||||||
| chr6:17413371
|
C | T | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-8184C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413371 | ||||||
| chr6:17413416
|
C | T | 2 | a0001c0001t0001g0085a0001c0002t0006g0133 | 2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-1-8139C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413416 | ||||||
| chr6:17413757
|
G | A | 3 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0002g0131 | 3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-1-7798G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413757 | ||||||
| chr6:17413875
|
G | A | 2 | a0001c0002t0001g0106a0001c0002t0001g0107 | 2 | HG00099.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-1-7680G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413875 | ||||||
| chr6:17413922
|
A | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(103): Show | 106 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(103): Show |
intron_variant | MODIFIER | c.-1-7633A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413922 | ||||||
| chr6:17413926
|
C | T | 2 | a0001c0002t0001g0188a0001c0002t0001g0189 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-1-7629C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413926 | ||||||
| chr6:17413927
|
G | A | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-1-7628G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413927 | ||||||
| chr6:17414053
|
CA | C | 39 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(36): Show | 39 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.-1-7487delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17414053 | |||||
| chr6:17414168
|
T | G | 1 | a0001c0002t0001g0183 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-1-7387T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414168 | ||||||
| chr6:17414261
|
C | CT | 28 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(25): Show | 28 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1-7284dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17414261 | |||||
| chr6:17414284
|
T | C | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-7271T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414284 | ||||||
| chr6:17414285
|
TA | T | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-7262delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17414285 | |||||
| chr6:17414299
|
T | A | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-7256T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414299 | ||||||
| chr6:17414342
|
A | G | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-7213A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414342 | ||||||
| chr6:17414344
|
G | T | 1 | a0002c0004t0002g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-1-7211G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414344 | ||||||
| chr6:17414461
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(103): Show | 106 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(103): Show |
intron_variant | MODIFIER | c.-1-7094A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414461 | ||||||
| chr6:17414468
|
A | G | 7 | a0001c0001t0002g0010a0001c0001t0002g0050a0001c0002t0001g0011others(4): Show | 7 | HG01361.hp2 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-7087A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414468 | ||||||
| chr6:17414485
|
A | G | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-7070A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414485 | ||||||
| chr6:17414597
|
C | T | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-6958C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414597 | ||||||
| chr6:17414993
|
C | T | 2 | a0001c0009t0001g0012a0002c0012t0001g0013 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-1-6562C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414993 | ||||||
| chr6:17415054
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-1-6501T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415054 | ||||||
| chr6:17415209
|
A | G | 2 | a0001c0002t0001g0132a0001c0003t0002g0131 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-1-6346A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415209 | ||||||
| chr6:17415286
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 86 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.-1-6269T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415286 | ||||||
| chr6:17415677
|
G | A | 12 | a0001c0001t0001g0069a0001c0001t0001g0202a0001c0001t0002g0199others(9): Show | 12 | HG01109.hp2 HG01255.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-5878G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415677 | ||||||
| chr6:17415758
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-1-5797G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415758 | ||||||
| chr6:17415822
|
A | G | 2 | a0001c0001t0002g0126a0001c0001t0002g0175 | 2 | NA18747.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-1-5733A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415822 | ||||||
| chr6:17415825
|
G | T | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-5730G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415825 | ||||||
| chr6:17415832
|
C | T | 1 | a0001c0002t0001g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-1-5723C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415832 | ||||||
| chr6:17415833
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(52): Show | 55 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.-1-5722G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415833 | ||||||
| chr6:17415931
|
A | C | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-5624A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415931 | ||||||
| chr6:17416027
|
T | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(52): Show | 55 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.-1-5528T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416027 | ||||||
| chr6:17416070
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-1-5485A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416070 | ||||||
| chr6:17416153
|
T | TGAGAAAA others(316): Show |
1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(323): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | |||||
| chr6:17416153
|
T | TGAGAAAA others(317): Show |
3 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0002g0037 | 3 | HG02258.hp2 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(324): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | |||||
| chr6:17416153
|
T | TGAGAAAA others(318): Show |
14 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0039others(11): Show | 14 | HG01106.hp1 HG01361.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(325): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | |||||
| chr6:17416153
|
T | TGAGAAAA others(319): Show |
20 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(17): Show | 20 | HG00099.hp1 HG01175.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(326): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | |||||
| chr6:17416153
|
T | TGAGAAAA others(320): Show |
14 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0028others(11): Show | 14 | HG01496.hp1 HG02027.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(327): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | |||||
| chr6:17416153
|
T | TGAGAAAA others(321): Show |
2 | a0001c0001t0001g0009a0001c0001t0001g0029 | 2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(328): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | |||||
| chr6:17416153
|
T | TGAGAAAA others(323): Show |
1 | a0001c0001t0002g0030 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(330): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | |||||
| chr6:17416212
|
G | T | 1 | a0003c0007t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-1-5343G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416212 | ||||||
| chr6:17416359
|
G | T | 3 | a0001c0009t0001g0014a0001c0013t0001g0092a0001c0014t0008g0015 | 3 | HG01361.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-5196G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416359 | ||||||
| chr6:17416528
|
G | A | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-1-5027G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416528 | ||||||
| chr6:17416554
|
G | A | 2 | a0001c0002t0001g0035a0001c0003t0001g0038 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-1-5001G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416554 | ||||||
| chr6:17416560
|
G | A | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-4995G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416560 | ||||||
| chr6:17416895
|
C | A | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-1-4660C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416895 | ||||||
| chr6:17416976
|
A | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(114): Show | 117 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(114): Show |
intron_variant | MODIFIER | c.-1-4579A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416976 | ||||||
| chr6:17416996
|
A | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(56): Show | 59 | HG00099.hp1 HG01071.hp1 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.-1-4559A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416996 | ||||||
| chr6:17417145
|
GA | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(65): Show | 68 | HG00099.hp1 HG01071.hp1 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.-1-4399delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17417145 | |||||
| chr6:17417247
|
A | C | 20 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0202others(17): Show | 20 | HG00741.hp2 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1-4308A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17417247 | ||||||
| chr6:17417274
|
A | AT | 40 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0034others(37): Show | 40 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.-1-4264dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17417274 | |||||
| chr6:17417274
|
AT | A | 7 | a0001c0001t0001g0052a0001c0002t0001g0130a0001c0002t0001g0132others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-4264delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17417274 | |||||
| chr6:17417326
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-1-4229A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17417326 | ||||||
| chr6:17417413
|
T | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(116): Show | 119 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(116): Show |
intron_variant | MODIFIER | c.-1-4142T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17417413 | ||||||
| chr6:17417420
|
C | T | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-4135C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17417420 | ||||||
| chr6:17417521
|
C | T | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-4034C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17417521 | ||||||
| chr6:17417963
|
G | A | 1 | a0001c0008t0001g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1-3592G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17417963 | ||||||
| chr6:17418085
|
G | C | 1 | a0001c0002t0001g0190 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-1-3470G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418085 | ||||||
| chr6:17418158
|
G | C | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-3397G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418158 | ||||||
| chr6:17418176
|
C | T | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-3379C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418176 | ||||||
| chr6:17418177
|
G | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(60): Show | 63 | HG00099.hp1 HG01071.hp1 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.-1-3378G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418177 | ||||||
| chr6:17418669
|
A | AT | 30 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(27): Show | 30 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.-1-2876dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17418669 | |||||
| chr6:17418682
|
A | G | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-2873A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418682 | ||||||
| chr6:17418756
|
G | A | 1 | a0001c0002t0001g0058 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-1-2799G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418756 | ||||||
| chr6:17418803
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-2752C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418803 | ||||||
| chr6:17419381
|
G | A | 5 | a0001c0001t0002g0010a0001c0001t0002g0050a0001c0002t0001g0011others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-2174G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419381 | ||||||
| chr6:17419426
|
G | A | 1 | a0001c0001t0002g0162 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-1-2129G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419426 | ||||||
| chr6:17419468
|
T | C | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-1-2087T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419468 | ||||||
| chr6:17419480
|
G | A | 5 | a0001c0002t0001g0197a0001c0003t0001g0065a0003c0007t0001g0059others(2): Show | 5 | HG01496.hp2 HG02280.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-2075G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419480 | ||||||
| chr6:17419548
|
A | T | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-2007A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419548 | ||||||
| chr6:17419899
|
G | C | 2 | a0001c0002t0001g0093a0001c0002t0001g0094 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-1-1656G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419899 | ||||||
| chr6:17419964
|
T | C | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-1591T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419964 | ||||||
| chr6:17420025
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(114): Show | 117 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(114): Show |
intron_variant | MODIFIER | c.-1-1530T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420025 | ||||||
| chr6:17420060
|
C | T | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-1495C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420060 | ||||||
| chr6:17420166
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.-1-1389A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420166 | ||||||
| chr6:17420311
|
C | T | 1 | a0001c0008t0001g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1-1244C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420311 | ||||||
| chr6:17420570
|
C | T | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-985C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420570 | ||||||
| chr6:17420882
|
G | T | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-1-673G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420882 | ||||||
| chr6:17420973
|
C | T | 2 | a0001c0001t0002g0126a0001c0001t0002g0175 | 2 | NA18747.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-1-582C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420973 | ||||||
| chr6:17420983
|
G | GT | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1-570dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17420983 | |||||
| chr6:17421072
|
A | G | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1-483A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17421072 | ||||||
| chr6:17421218
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-1-337C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17421218 | ||||||
| chr6:17421251
|
G | A | 15 | a0001c0001t0001g0052a0001c0001t0002g0055a0001c0002t0001g0056others(12): Show | 15 | HG00741.hp2 HG01168.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1-304G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17421251 | ||||||
| chr6:17421793
|
C | T | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.121+117C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17421793 | ||||||
| chr6:17421838
|
A | G | 5 | a0001c0001t0002g0010a0001c0001t0002g0050a0001c0002t0001g0011others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+162A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17421838 | ||||||
| chr6:17421855
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0078 | 2 | HG01167.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.121+179C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17421855 | ||||||
| chr6:17421981
|
C | G | 5 | a0001c0001t0002g0010a0001c0001t0002g0050a0001c0002t0001g0011others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+305C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17421981 | ||||||
| chr6:17422008
|
G | A | 1 | a0001c0008t0001g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.121+332G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17422008 | ||||||
| chr6:17422305
|
C | T | 15 | a0001c0001t0001g0052a0001c0001t0002g0055a0001c0002t0001g0056others(12): Show | 15 | HG00741.hp2 HG01168.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.121+629C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17422305 | ||||||
| chr6:17422346
|
CT | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(98): Show | 101 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(98): Show |
intron_variant | MODIFIER | c.121+691delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 17422346 | |||||
| chr6:17422498
|
C | T | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.121+822C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17422498 | ||||||
| chr6:17422628
|
C | T | 1 | a0001c0002t0001g0173 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.121+952C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17422628 | ||||||
| chr6:17422912
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.121+1236T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17422912 | ||||||
| chr6:17422974
|
A | G | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.121+1298A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17422974 | ||||||
| chr6:17423044
|
T | C | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.121+1368T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17423044 | ||||||
| chr6:17423704
|
T | C | 1 | a0001c0002t0001g0193 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.121+2028T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17423704 | ||||||
| chr6:17423845
|
A | G | 4 | a0001c0001t0001g0069a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 4 | HG02615.hp2 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+2169A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17423845 | ||||||
| chr6:17424018
|
C | A | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.121+2342C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424018 | ||||||
| chr6:17424126
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(119): Show | 122 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(119): Show |
intron_variant | MODIFIER | c.121+2450A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424126 | ||||||
| chr6:17424177
|
G | A | 1 | a0001c0009t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.122-2413G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424177 | ||||||
| chr6:17424225
|
T | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122-2365T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424225 | ||||||
| chr6:17424228
|
G | A | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122-2362G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424228 | ||||||
| chr6:17424243
|
G | A | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122-2347G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424243 | ||||||
| chr6:17424244
|
A | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122-2346A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424244 | ||||||
| chr6:17424256
|
T | C | 2 | a0001c0008t0001g0051a0001c0013t0001g0092 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.122-2334T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424256 | ||||||
| chr6:17424262
|
T | C | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122-2328T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424262 | ||||||
| chr6:17424263
|
G | A | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122-2327G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424263 | ||||||
| chr6:17424269
|
G | A | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.122-2321G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424269 | ||||||
| chr6:17424306
|
A | G | 26 | a0001c0001t0001g0154a0001c0001t0001g0159a0001c0001t0001g0179others(23): Show | 26 | HG00438.hp2 HG00609.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.122-2284A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424306 | ||||||
| chr6:17424365
|
A | T | 13 | a0001c0001t0001g0052a0001c0001t0002g0055a0001c0002t0001g0056others(10): Show | 13 | HG00741.hp2 HG01168.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-2225A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424365 | ||||||
| chr6:17424381
|
C | A | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122-2209C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424381 | ||||||
| chr6:17424426
|
G | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 53 | HG00099.hp1 HG01071.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.122-2164G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424426 | ||||||
| chr6:17424587
|
C | T | 1 | a0001c0008t0001g0204 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.122-2003C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424587 | ||||||
| chr6:17425067
|
A | T | 1 | a0001c0008t0001g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.122-1523A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425067 | ||||||
| chr6:17425323
|
G | A | 1 | a0001c0003t0002g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.122-1267G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425323 | ||||||
| chr6:17425387
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.122-1203T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425387 | ||||||
| chr6:17425395
|
C | A | 1 | a0001c0001t0001g0029 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.122-1195C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425395 | ||||||
| chr6:17425587
|
C | A | 44 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(41): Show | 44 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.122-1003C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425587 | ||||||
| chr6:17425745
|
G | A | 8 | a0001c0001t0001g0069a0001c0002t0001g0144a0001c0002t0001g0145others(5): Show | 8 | HG01496.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.122-845G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425745 | ||||||
| chr6:17425811
|
A | G | 1 | a0001c0002t0001g0094 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.122-779A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425811 | ||||||
| chr6:17425815
|
C | A | 2 | a0001c0009t0001g0012a0002c0012t0001g0013 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.122-775C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425815 | ||||||
| chr6:17425870
|
C | G | 1 | a0001c0001t0001g0001 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.122-720C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425870 | ||||||
| chr6:17425936
|
A | T | 1 | a0001c0001t0002g0023 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.122-654A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425936 | ||||||
| chr6:17426051
|
C | T | 1 | a0001c0002t0001g0058 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.122-539C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426051 | ||||||
| chr6:17426099
|
C | A | 2 | a0001c0002t0001g0058a0001c0013t0001g0092 | 2 | HG00642.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.122-491C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426099 | ||||||
| chr6:17426103
|
C | A | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122-487C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426103 | ||||||
| chr6:17426115
|
C | A | 2 | a0001c0001t0002g0010a0001c0002t0001g0011 | 2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.122-475C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426115 | ||||||
| chr6:17426231
|
CT | C | 16 | a0001c0001t0001g0052a0001c0001t0001g0142a0001c0001t0002g0055others(13): Show | 16 | HG00642.hp1 HG00741.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.122-343delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 17426231 | |||||
| chr6:17426232
|
T | G | 1 | a0001c0001t0001g0025 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.122-358T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426232 | ||||||
| chr6:17426370
|
G | T | 29 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(26): Show | 29 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.122-220G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426370 | ||||||
| chr6:17426491
|
T | C | 13 | a0001c0001t0001g0052a0001c0001t0002g0055a0001c0002t0001g0056others(10): Show | 13 | HG00741.hp2 HG01168.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-99T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426491 | ||||||
| chr6:17426555
|
C | T | 2 | a0001c0001t0001g0095a0001c0002t0001g0002 | 2 | HG00438.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.122-35C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426555 | ||||||
| chr6:17426902
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(55): Show | 58 | HG00099.hp1 HG01071.hp1 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.222+212G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17426902 | ||||||
| chr6:17426935
|
A | T | 34 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(31): Show | 34 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.222+245A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17426935 | ||||||
| chr6:17426984
|
T | A | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+294T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17426984 | ||||||
| chr6:17427043
|
C | A | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.222+353C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427043 | ||||||
| chr6:17427308
|
C | T | 34 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(31): Show | 34 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.222+618C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427308 | ||||||
| chr6:17427350
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.222+660C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427350 | ||||||
| chr6:17427548
|
G | A | 29 | a0001c0001t0001g0009a0001c0001t0001g0067a0001c0001t0001g0068others(26): Show | 29 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.222+858G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427548 | ||||||
| chr6:17427608
|
C | CA | 22 | a0001c0001t0001g0052a0001c0001t0001g0069a0001c0001t0002g0055others(19): Show | 22 | HG00741.hp2 HG01168.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.222+933dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17427608 | |||||
| chr6:17427608
|
CA | C | 35 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(32): Show | 35 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.222+933delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17427608 | |||||
| chr6:17427625
|
G | A | 61 | a0001c0001t0001g0052a0001c0001t0001g0067a0001c0001t0001g0068others(58): Show | 61 | HG00735.hp2 HG00741.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.222+935G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427625 | ||||||
| chr6:17427634
|
G | A | 56 | a0001c0001t0001g0052a0001c0001t0001g0067a0001c0001t0001g0068others(53): Show | 56 | HG00735.hp2 HG00741.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.222+944G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427634 | ||||||
| chr6:17427970
|
T | C | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.222+1280T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427970 | ||||||
| chr6:17428012
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.222+1322C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428012 | ||||||
| chr6:17428023
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+1333G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428023 | ||||||
| chr6:17428393
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.222+1703C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428393 | ||||||
| chr6:17428476
|
A | G | 8 | a0001c0001t0001g0069a0001c0002t0001g0144a0001c0002t0001g0145others(5): Show | 8 | HG01496.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+1786A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428476 | ||||||
| chr6:17428540
|
C | T | 1 | a0001c0003t0001g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.222+1850C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428540 | ||||||
| chr6:17428628
|
A | G | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.222+1938A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428628 | ||||||
| chr6:17428630
|
G | C | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.222+1940G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428630 | ||||||
| chr6:17428774
|
T | TA | 58 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(55): Show | 58 | HG00099.hp1 HG01071.hp1 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.222+2095dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17428774 | |||||
| chr6:17428896
|
G | A | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.222+2206G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428896 | ||||||
| chr6:17429135
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.222+2445T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429135 | ||||||
| chr6:17429325
|
T | C | 5 | a0001c0008t0001g0051a0001c0009t0001g0012a0001c0009t0001g0014others(2): Show | 5 | HG01361.hp2 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+2635T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429325 | ||||||
| chr6:17429379
|
G | T | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+2689G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429379 | ||||||
| chr6:17429380
|
G | A | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+2690G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429380 | ||||||
| chr6:17429381
|
A | ACATCATA others(12): Show |
1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+2691_222+2692i others(21): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429381 | ||||||
| chr6:17429382
|
G | A | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+2692G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429382 | ||||||
| chr6:17429385
|
T | A | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+2695T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429385 | ||||||
| chr6:17429497
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.222+2807G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429497 | ||||||
| chr6:17429505
|
A | G | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.222+2815A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429505 | ||||||
| chr6:17429632
|
C | T | 3 | a0001c0008t0001g0051a0001c0009t0001g0014a0001c0014t0008g0015 | 3 | HG01361.hp2 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.222+2942C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429632 | ||||||
| chr6:17429947
|
C | T | 28 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(25): Show | 28 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.222+3257C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429947 | ||||||
| chr6:17429983
|
A | G | 1 | a0001c0002t0002g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.222+3293A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429983 | ||||||
| chr6:17430167
|
A | G | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+3477A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430167 | ||||||
| chr6:17430212
|
A | G | 2 | a0001c0009t0001g0012a0002c0012t0001g0013 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.222+3522A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430212 | ||||||
| chr6:17430507
|
C | A | 1 | a0001c0008t0001g0204 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.222+3817C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430507 | ||||||
| chr6:17430540
|
G | GT | 32 | a0001c0001t0001g0018a0001c0001t0001g0052a0001c0001t0002g0010others(29): Show | 32 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.222+3865dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17430540 | |||||
| chr6:17430607
|
G | C | 3 | a0001c0008t0001g0051a0001c0009t0001g0014a0001c0014t0008g0015 | 3 | HG01361.hp2 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.222+3917G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430607 | ||||||
| chr6:17430621
|
C | T | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+3931C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430621 | ||||||
| chr6:17430683
|
C | T | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+3993C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430683 | ||||||
| chr6:17430719
|
C | T | 8 | a0001c0001t0001g0069a0001c0002t0001g0144a0001c0002t0001g0145others(5): Show | 8 | HG01496.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+4029C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430719 | ||||||
| chr6:17430819
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.222+4129G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430819 | ||||||
| chr6:17430898
|
A | T | 11 | a0001c0001t0001g0069a0001c0002t0001g0144a0001c0002t0001g0145others(8): Show | 11 | HG01361.hp2 HG01496.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.222+4208A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430898 | ||||||
| chr6:17430926
|
A | G | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.222+4236A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430926 | ||||||
| chr6:17431194
|
C | G | 1 | a0001c0001t0001g0004 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.222+4504C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431194 | ||||||
| chr6:17431290
|
C | T | 1 | a0004c0010t0001g0063 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.222+4600C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431290 | ||||||
| chr6:17431324
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+4634G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431324 | ||||||
| chr6:17431371
|
A | G | 5 | a0001c0008t0001g0051a0001c0009t0001g0012a0001c0009t0001g0014others(2): Show | 5 | HG01361.hp2 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+4681A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431371 | ||||||
| chr6:17431390
|
A | C | 4 | a0001c0001t0001g0069a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 4 | HG02615.hp2 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+4700A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431390 | ||||||
| chr6:17431478
|
A | G | 28 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(25): Show | 28 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.222+4788A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431478 | ||||||
| chr6:17431655
|
G | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(121): Show | 124 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(121): Show |
intron_variant | MODIFIER | c.222+4965G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431655 | ||||||
| chr6:17431851
|
T | C | 1 | a0001c0001t0002g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.222+5161T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431851 | ||||||
| chr6:17431856
|
G | A | 1 | a0001c0003t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.222+5166G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431856 | ||||||
| chr6:17431931
|
G | A | 1 | a0001c0001t0002g0162 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.222+5241G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431931 | ||||||
| chr6:17432057
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+5367G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432057 | ||||||
| chr6:17432142
|
G | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(121): Show | 124 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(121): Show |
intron_variant | MODIFIER | c.222+5452G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432142 | ||||||
| chr6:17432178
|
A | C | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+5488A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432178 | ||||||
| chr6:17432604
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(50): Show | 53 | HG00099.hp1 HG00741.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.222+5914C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432604 | ||||||
| chr6:17432633
|
A | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+5943A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432633 | ||||||
| chr6:17432664
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 53 | HG00099.hp1 HG00741.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.222+5974T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432664 | ||||||
| chr6:17432719
|
C | CCTTG | 170 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.222+6041_222+6044d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17432719 | |||||
| chr6:17432886
|
G | A | 1 | a0001c0003t0001g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.222+6196G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432886 | ||||||
| chr6:17432962
|
T | TC | 8 | a0001c0001t0001g0039a0001c0001t0001g0154a0001c0001t0001g0185others(5): Show | 8 | HG00642.hp2 HG01192.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+6278dupC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17432962 | |||||
| chr6:17432969
|
T | C | 3 | a0001c0002t0001g0058a0001c0008t0001g0057a0002c0004t0001g0089 | 3 | HG00642.hp1 HG00735.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.222+6279T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432969 | ||||||
| chr6:17433046
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.222+6356A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433046 | ||||||
| chr6:17433090
|
G | A | 3 | a0001c0002t0001g0058a0001c0008t0001g0057a0002c0004t0001g0089 | 3 | HG00642.hp1 HG00735.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.222+6400G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433090 | ||||||
| chr6:17433142
|
G | A | 24 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(21): Show | 24 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.222+6452G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433142 | ||||||
| chr6:17433166
|
A | G | 14 | a0001c0001t0001g0069a0001c0001t0001g0099a0001c0002t0001g0062others(11): Show | 14 | HG01255.hp1 HG01361.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.222+6476A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433166 | ||||||
| chr6:17433333
|
G | A | 12 | a0001c0001t0001g0069a0001c0002t0001g0058a0001c0002t0001g0144others(9): Show | 12 | HG00642.hp1 HG01361.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.222+6643G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433333 | ||||||
| chr6:17433572
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.222+6882A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433572 | ||||||
| chr6:17433661
|
C | T | 1 | a0001c0001t0007g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.222+6971C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433661 | ||||||
| chr6:17433720
|
G | A | 16 | a0001c0001t0001g0069a0001c0001t0002g0010a0001c0002t0001g0011others(13): Show | 16 | HG00642.hp1 HG01255.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.222+7030G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433720 | ||||||
| chr6:17433759
|
T | C | 4 | a0001c0001t0002g0010a0001c0002t0001g0011a0001c0002t0001g0062others(1): Show | 4 | HG01255.hp1 HG02109.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+7069T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433759 | ||||||
| chr6:17433828
|
A | G | 2 | a0001c0001t0002g0181a0001c0002t0001g0098 | 2 | NA18939.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.222+7138A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433828 | ||||||
| chr6:17433924
|
C | T | 23 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(20): Show | 23 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.222+7234C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433924 | ||||||
| chr6:17434046
|
C | T | 7 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0001g0065others(4): Show | 7 | HG01496.hp2 HG02280.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+7356C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434046 | ||||||
| chr6:17434231
|
C | CT | 5 | a0001c0003t0002g0060a0001c0003t0002g0064a0001c0003t0002g0087others(2): Show | 5 | HG01361.hp2 HG02109.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+7544dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17434231 | |||||
| chr6:17434231
|
C | CTT | 5 | a0001c0001t0001g0069a0001c0002t0001g0002a0001c0002t0001g0144others(2): Show | 5 | HG02258.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+7543_222+7544d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17434231 | |||||
| chr6:17434235
|
C | CT | 22 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0078others(19): Show | 22 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.222+7556dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17434235 | |||||
| chr6:17434235
|
C | CTT | 8 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(5): Show | 8 | HG01167.hp2 HG01884.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+7555_222+7556d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17434235 | |||||
| chr6:17434235
|
C | T | 11 | a0001c0001t0001g0069a0001c0002t0001g0002a0001c0002t0001g0144others(8): Show | 11 | HG01361.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+7545C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434235 | ||||||
| chr6:17434235
|
CT | C | 7 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0001g0065others(4): Show | 7 | HG01496.hp2 HG02280.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+7556delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17434235 | |||||
| chr6:17434417
|
C | G | 23 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(20): Show | 23 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.222+7727C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434417 | ||||||
| chr6:17434481
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.222+7791G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434481 | ||||||
| chr6:17434636
|
A | G | 25 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.222+7946A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434636 | ||||||
| chr6:17434646
|
A | G | 11 | a0001c0001t0001g0069a0001c0002t0001g0002a0001c0002t0001g0144others(8): Show | 11 | HG01361.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+7956A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434646 | ||||||
| chr6:17434848
|
AC | A | 11 | a0001c0001t0001g0069a0001c0002t0001g0002a0001c0002t0001g0144others(8): Show | 11 | HG01361.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+8162delC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17434848 | |||||
| chr6:17434867
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.222+8177G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434867 | ||||||
| chr6:17434976
|
A | G | 9 | a0001c0001t0001g0099a0001c0002t0001g0100a0001c0002t0001g0130others(6): Show | 9 | HG01496.hp2 HG02280.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+8286A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434976 | ||||||
| chr6:17434977
|
T | G | 11 | a0001c0001t0001g0069a0001c0002t0001g0002a0001c0002t0001g0144others(8): Show | 11 | HG01361.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+8287T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434977 | ||||||
| chr6:17435051
|
G | A | 11 | a0001c0001t0001g0069a0001c0002t0001g0002a0001c0002t0001g0144others(8): Show | 11 | HG01361.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+8361G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435051 | ||||||
| chr6:17435206
|
A | G | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.222+8516A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435206 | ||||||
| chr6:17435211
|
G | T | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+8521G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435211 | ||||||
| chr6:17435545
|
G | C | 9 | a0001c0001t0001g0099a0001c0002t0001g0100a0001c0002t0001g0130others(6): Show | 9 | HG01496.hp2 HG02280.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+8855G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435545 | ||||||
| chr6:17435605
|
G | A | 4 | a0001c0001t0002g0010a0001c0002t0001g0011a0001c0002t0001g0062others(1): Show | 4 | HG01255.hp1 HG02109.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+8915G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435605 | ||||||
| chr6:17435673
|
G | A | 2 | a0001c0001t0002g0181a0001c0002t0001g0098 | 2 | NA18939.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.222+8983G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435673 | ||||||
| chr6:17435681
|
TA | T | 90 | a0001c0001t0001g0028a0001c0001t0001g0048a0001c0001t0001g0052others(87): Show | 90 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.222+9014delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435681 | |||||
| chr6:17435681
|
TAA | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.222+9013_222+9014d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435681 | |||||
| chr6:17435681
|
TAAA | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0029others(4): Show | 7 | HG02083.hp1 HG02486.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+9012_222+9014d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435681 | |||||
| chr6:17435681
|
TAAAA | T | 27 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(24): Show | 27 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.222+9011_222+9014d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435681 | |||||
| chr6:17435702
|
A | G | 15 | a0001c0001t0001g0069a0001c0001t0002g0010a0001c0002t0001g0002others(12): Show | 15 | HG01255.hp1 HG01361.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.222+9012A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435702 | ||||||
| chr6:17435717
|
T | TA | 7 | a0001c0001t0001g0034a0001c0001t0001g0127a0001c0001t0002g0023others(4): Show | 7 | HG01175.hp1 HG02027.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+9042dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435717 | |||||
| chr6:17435717
|
TA | T | 7 | a0001c0001t0001g0140a0001c0001t0002g0050a0001c0002t0001g0191others(4): Show | 7 | HG00735.hp2 HG01516.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+9042delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435717 | |||||
| chr6:17435717
|
TAAA | T | 9 | a0001c0001t0001g0099a0001c0002t0001g0100a0001c0002t0001g0130others(6): Show | 9 | HG01496.hp2 HG02280.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+9040_222+9042d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435717 | |||||
| chr6:17435727
|
AAAAAAC | A | 9 | a0001c0001t0001g0069a0001c0002t0001g0144a0001c0002t0001g0145others(6): Show | 9 | HG01361.hp2 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+9043_222+9048d others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435727 | |||||
| chr6:17435732
|
A | C | 6 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0002g0199others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+9042A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435732 | ||||||
| chr6:17435733
|
C | A | 7 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0002g0010others(4): Show | 7 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+9043C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435733 | ||||||
| chr6:17435742
|
A | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.222+9052A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435742 | ||||||
| chr6:17436061
|
T | C | 11 | a0001c0001t0001g0069a0001c0002t0001g0002a0001c0002t0001g0144others(8): Show | 11 | HG01361.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+9371T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436061 | ||||||
| chr6:17436067
|
A | ATCTTTCT others(1): Show |
4 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0144others(1): Show | 4 | HG01255.hp1 HG02258.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+9392_222+9399d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436067 | |||||
| chr6:17436067
|
A | ATCTTTCT others(5): Show |
1 | a0001c0001t0002g0010 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.222+9388_222+9399d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436067 | |||||
| chr6:17436067
|
A | ATCTTTCT others(9): Show |
1 | a0001c0002t0001g0145 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.222+9384_222+9399d others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436067 | |||||
| chr6:17436078
|
T | TTTCCTTC others(5): Show |
1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.222+9391_222+9392i others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436078 | |||||
| chr6:17436078
|
T | TTTCCTTC others(9): Show |
3 | a0001c0001t0001g0202a0001c0001t0002g0199a0001c0001t0007g0201 | 3 | HG01109.hp2 HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.222+9391_222+9392i others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436078 | |||||
| chr6:17436078
|
T | TTTCCTTC others(13): Show |
2 | a0001c0001t0001g0196a0001c0001t0005g0200 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.222+9391_222+9392i others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436078 | |||||
| chr6:17436082
|
T | C | 6 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0002g0199others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+9392T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436082 | ||||||
| chr6:17436082
|
T | TTTCCTTC others(5): Show |
7 | a0001c0001t0001g0099a0001c0002t0001g0100a0001c0002t0001g0130others(4): Show | 7 | HG01496.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+9395_222+9396i others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436082 | |||||
| chr6:17436082
|
T | TTTCCTTC others(9): Show |
1 | a0001c0002t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.222+9395_222+9396i others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436082 | |||||
| chr6:17436082
|
T | TTTCCTTC others(13): Show |
1 | a0003c0007t0001g0059 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.222+9395_222+9396i others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436082 | |||||
| chr6:17436086
|
T | C | 16 | a0001c0001t0001g0099a0001c0001t0001g0196a0001c0001t0001g0202others(13): Show | 16 | HG01109.hp2 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.222+9396T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436086 | ||||||
| chr6:17436086
|
T | TTTCC | 13 | a0001c0001t0001g0095a0001c0001t0002g0147a0001c0001t0002g0162others(10): Show | 13 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.222+9429_222+9432d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | |||||
| chr6:17436086
|
T | TTTCCTTC others(1): Show |
17 | a0001c0001t0001g0067a0001c0001t0001g0074a0001c0001t0001g0075others(14): Show | 17 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.222+9425_222+9432d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | |||||
| chr6:17436086
|
T | TTTCCTTC others(5): Show |
4 | a0001c0001t0001g0068a0001c0003t0001g0091a0002c0004t0002g0077others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+9421_222+9432d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | |||||
| chr6:17436086
|
T | TTTCTTTC others(1): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0002t0001g0019 | 3 | HG01978.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.222+9399_222+9400i others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | |||||
| chr6:17436086
|
T | TTTCTTTC others(5): Show |
50 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.222+9399_222+9400i others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | |||||
| chr6:17436086
|
T | TTTCTTTC others(9): Show |
4 | a0001c0001t0001g0041a0001c0001t0002g0037a0001c0002t0002g0129others(1): Show | 4 | HG01167.hp1 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+9399_222+9400i others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | |||||
| chr6:17436086
|
T | TTTCTTTC others(13): Show |
1 | a0001c0001t0001g0032 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.222+9399_222+9400i others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | |||||
| chr6:17436086
|
TTTCC | T | 3 | a0002c0012t0001g0013a0003c0007t0001g0110a0003c0007t0001g0119 | 3 | HG01106.hp2 HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.222+9429_222+9432d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | |||||
| chr6:17436090
|
C | T | 15 | a0001c0001t0001g0069a0001c0001t0002g0010a0001c0002t0001g0002others(12): Show | 15 | HG01255.hp1 HG01361.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.222+9400C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436090 | ||||||
| chr6:17436094
|
C | T | 14 | a0001c0001t0001g0069a0001c0001t0002g0010a0001c0002t0001g0011others(11): Show | 14 | HG01255.hp1 HG01361.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.222+9404C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436094 | ||||||
| chr6:17436098
|
C | T | 4 | a0001c0001t0001g0069a0001c0002t0001g0062a0001c0002t0001g0198others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+9408C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436098 | ||||||
| chr6:17436119
|
T | C | 11 | a0001c0001t0002g0010a0001c0002t0001g0002a0001c0002t0001g0011others(8): Show | 11 | HG01255.hp1 HG01361.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+9429T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436119 | ||||||
| chr6:17436123
|
C | CTCCT | 8 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0069others(5): Show | 8 | HG01168.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+9447_222+9450d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436123 | |||||
| chr6:17436123
|
C | T | 11 | a0001c0001t0002g0010a0001c0002t0001g0002a0001c0002t0001g0011others(8): Show | 11 | HG01255.hp1 HG01361.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+9433C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436123 | ||||||
| chr6:17436284
|
A | G | 25 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(22): Show | 25 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.222+9594A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436284 | ||||||
| chr6:17436585
|
G | A | 4 | a0001c0003t0002g0060a0001c0003t0002g0064a0001c0003t0002g0087others(1): Show | 4 | HG02109.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+9895G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436585 | ||||||
| chr6:17437002
|
G | A | 6 | a0001c0001t0001g0069a0001c0002t0001g0002a0001c0002t0001g0144others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+10312G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437002 | ||||||
| chr6:17437261
|
CTGGTCTA others(3): Show |
C | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051 | 3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.222+10572_222+1058 others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437261 | ||||||
| chr6:17437433
|
A | G | 2 | a0001c0002t0001g0062a0004c0010t0002g0061 | 2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.222+10743A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437433 | ||||||
| chr6:17437504
|
T | C | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.222+10814T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437504 | ||||||
| chr6:17437649
|
C | T | 1 | a0001c0002t0001g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.222+10959C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437649 | ||||||
| chr6:17437650
|
G | A | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+10960G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437650 | ||||||
| chr6:17437737
|
C | T | 2 | a0001c0002t0001g0058a0001c0008t0001g0057 | 2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.222+11047C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437737 | ||||||
| chr6:17437803
|
G | C | 3 | a0001c0001t0002g0157a0001c0002t0001g0056a0001c0002t0001g0153 | 3 | HG03491.hp2 HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.222+11113G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437803 | ||||||
| chr6:17437834
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.222+11144G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437834 | ||||||
| chr6:17437856
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0002g0055 | 3 | HG01168.hp1 HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.222+11166G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437856 | ||||||
| chr6:17437870
|
G | A | 15 | a0001c0001t0001g0069a0001c0001t0002g0010a0001c0002t0001g0002others(12): Show | 15 | HG01255.hp1 HG01361.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.222+11180G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437870 | ||||||
| chr6:17437964
|
G | C | 2 | a0001c0002t0001g0062a0004c0010t0002g0061 | 2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.222+11274G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437964 | ||||||
| chr6:17438011
|
C | T | 2 | a0001c0002t0001g0062a0004c0010t0002g0061 | 2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.222+11321C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438011 | ||||||
| chr6:17438053
|
A | C | 9 | a0001c0001t0001g0099a0001c0002t0001g0100a0001c0002t0001g0130others(6): Show | 9 | HG01496.hp2 HG02280.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+11363A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438053 | ||||||
| chr6:17438064
|
A | AGTG | 5 | a0001c0001t0001g0069a0001c0002t0001g0144a0001c0002t0001g0145others(2): Show | 5 | HG02486.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+11374_222+1137 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438064 | ||||||
| chr6:17438066
|
G | C | 5 | a0001c0001t0001g0069a0001c0002t0001g0144a0001c0002t0001g0145others(2): Show | 5 | HG02486.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+11376G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438066 | ||||||
| chr6:17438069
|
T | TG | 5 | a0001c0001t0001g0069a0001c0002t0001g0144a0001c0002t0001g0145others(2): Show | 5 | HG02486.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+11379_222+1138 others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438069 | ||||||
| chr6:17438071
|
GATTATAA others(3602): Show |
G | 5 | a0001c0001t0001g0069a0001c0002t0001g0144a0001c0002t0001g0145others(2): Show | 5 | HG02486.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+11382_222+1499 others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438071 | ||||||
| chr6:17438121
|
G | T | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+11431G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438121 | ||||||
| chr6:17438173
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.222+11483T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438173 | ||||||
| chr6:17438194
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0002g0050 | 2 | HG02486.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.222+11504C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438194 | ||||||
| chr6:17438355
|
GATT | G | 141 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(138): Show | 141 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.222+11666_222+1166 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438355 | ||||||
| chr6:17438393
|
A | T | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+11703A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438393 | ||||||
| chr6:17438401
|
T | G | 97 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(94): Show | 97 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.222+11711T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438401 | ||||||
| chr6:17438404
|
T | G | 140 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(137): Show | 140 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.222+11714T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438404 | ||||||
| chr6:17438431
|
G | GTAT | 3 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0002g0131 | 3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.222+11742_222+1174 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438431 | |||||
| chr6:17438431
|
G | GTGTTT | 74 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(71): Show | 74 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.222+11743_222+1174 others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438431 | |||||
| chr6:17438433
|
G | GT | 19 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0016others(16): Show | 19 | HG00642.hp2 HG01106.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.222+11766dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | |||||
| chr6:17438433
|
G | GTTT | 5 | a0001c0001t0001g0099a0001c0002t0001g0058a0001c0002t0001g0100others(2): Show | 5 | HG00642.hp1 HG01496.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+11764_222+1176 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | |||||
| chr6:17438433
|
G | GTTTTGT | 19 | a0001c0001t0001g0034a0001c0001t0001g0054a0001c0001t0001g0103others(16): Show | 19 | HG00597.hp1 HG00597.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.222+11747_222+1174 others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | |||||
| chr6:17438433
|
G | GTTTTGTT others(4): Show |
8 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0078others(5): Show | 8 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+11747_222+1174 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | |||||
| chr6:17438433
|
G | GTTTTGTT others(5): Show |
8 | a0001c0001t0001g0076a0001c0003t0001g0082a0001c0003t0002g0060others(5): Show | 8 | HG01361.hp2 HG02897.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+11747_222+1174 others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | |||||
| chr6:17438433
|
G | GTTTTGTT others(6): Show |
1 | a0001c0003t0002g0087 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.222+11747_222+1174 others(17): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | |||||
| chr6:17438433
|
G | GTTTTTTT others(1): Show |
6 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0003t0001g0088others(3): Show | 6 | HG02622.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+11759_222+1176 others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | |||||
| chr6:17438433
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0001g0067a0001c0002t0001g0197 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.222+11757_222+1176 others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | |||||
| chr6:17438433
|
G | GTTTTTTT others(4): Show |
1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+11756_222+1176 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | |||||
| chr6:17438433
|
G | T | 3 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0002g0131 | 3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.222+11743G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438433 | ||||||
| chr6:17438584
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.222+11894G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438584 | ||||||
| chr6:17438600
|
A | G | 141 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(138): Show | 141 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.222+11910A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438600 | ||||||
| chr6:17438640
|
A | C | 10 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0002g0199others(7): Show | 10 | HG01109.hp2 HG01361.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+11950A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438640 | ||||||
| chr6:17438641
|
G | A | 5 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0002g0199others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+11951G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438641 | ||||||
| chr6:17438643
|
G | A | 94 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(91): Show | 94 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.222+11953G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438643 | ||||||
| chr6:17438674
|
T | C | 2 | a0001c0001t0001g0127a0001c0002t0001g0128 | 2 | HG01071.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.222+11984T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438674 | ||||||
| chr6:17438681
|
C | T | 2 | a0001c0001t0001g0127a0001c0002t0001g0128 | 2 | HG01071.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.222+11991C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438681 | ||||||
| chr6:17438686
|
A | G | 2 | a0001c0001t0001g0127a0001c0002t0001g0128 | 2 | HG01071.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.222+11996A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438686 | ||||||
| chr6:17438690
|
C | T | 2 | a0001c0001t0001g0127a0001c0002t0001g0128 | 2 | HG01071.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.222+12000C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438690 | ||||||
| chr6:17438714
|
T | C | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0086others(7): Show | 10 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+12024T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438714 | ||||||
| chr6:17438718
|
T | C | 142 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0048others(139): Show | 142 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.222+12028T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438718 | ||||||
| chr6:17438745
|
T | G | 119 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(116): Show | 119 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.222+12055T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438745 | ||||||
| chr6:17438779
|
CTT | C | 140 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(137): Show | 140 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.222+12098_222+1209 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438779 | |||||
| chr6:17438802
|
A | G | 140 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(137): Show | 140 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.222+12112A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438802 | ||||||
| chr6:17438850
|
C | T | 140 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(137): Show | 140 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.222+12160C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438850 | ||||||
| chr6:17438930
|
G | A | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.222+12240G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438930 | ||||||
| chr6:17438968
|
G | A | 1 | a0001c0002t0001g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.222+12278G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438968 | ||||||
| chr6:17439147
|
A | G | 5 | a0001c0003t0002g0060a0001c0003t0002g0064a0001c0003t0002g0087others(2): Show | 5 | HG01361.hp2 HG02109.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+12457A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17439147 | ||||||
| chr6:17439255
|
G | GT | 134 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(131): Show | 134 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.222+12577dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17439255 | |||||
| chr6:17439255
|
G | GTT | 9 | a0001c0001t0001g0124a0001c0001t0002g0199a0001c0002t0001g0134others(6): Show | 9 | HG01361.hp2 HG02109.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+12576_222+1257 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17439255 | |||||
| chr6:17439728
|
T | G | 22 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(19): Show | 22 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.222+13038T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17439728 | ||||||
| chr6:17439760
|
T | C | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+13070T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17439760 | ||||||
| chr6:17439775
|
G | A | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+13085G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17439775 | ||||||
| chr6:17439847
|
T | G | 1 | a0001c0014t0008g0015 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.222+13157T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17439847 | ||||||
| chr6:17439974
|
A | G | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+13284A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17439974 | ||||||
| chr6:17440021
|
T | C | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+13331T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440021 | ||||||
| chr6:17440150
|
T | C | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+13460T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440150 | ||||||
| chr6:17440527
|
A | T | 2 | a0001c0001t0001g0085a0002c0004t0001g0089 | 2 | HG00735.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.222+13837A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440527 | ||||||
| chr6:17440606
|
C | CTGTGTGG | 16 | a0001c0001t0001g0142a0001c0001t0001g0180a0001c0001t0001g0196others(13): Show | 16 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.222+13922_222+1392 others(11): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440606 | |||||
| chr6:17440606
|
C | CTGTGTGG others(2): Show |
3 | a0001c0001t0002g0105a0001c0001t0002g0121a0001c0001t0002g0157 | 3 | HG01928.hp2 HG01952.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.222+13922_222+1392 others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440606 | |||||
| chr6:17440606
|
C | CTGTGTGG others(4): Show |
1 | a0001c0002t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.222+13922_222+1392 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440606 | |||||
| chr6:17440606
|
CTG | C | 17 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(14): Show | 17 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.222+13923_222+1392 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440606 | |||||
| chr6:17440607
|
T | TGTGTG | 59 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(56): Show | 59 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.222+13918_222+1392 others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440607 | |||||
| chr6:17440609
|
T | TGTG | 17 | a0001c0001t0001g0068a0001c0001t0001g0095a0001c0001t0002g0150others(14): Show | 17 | HG00438.hp1 HG00609.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.222+13920_222+1392 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440609 | |||||
| chr6:17440611
|
T | TG | 17 | a0001c0001t0001g0099a0001c0001t0002g0122a0001c0001t0002g0172others(14): Show | 17 | HG00642.hp1 HG01243.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.222+13922dupG | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440611 | |||||
| chr6:17440613
|
T | G | 8 | a0001c0001t0001g0067a0001c0002t0001g0130a0001c0002t0001g0132others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+13923T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440613 | ||||||
| chr6:17440614
|
G | GGTGT | 33 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(30): Show | 33 | HG01071.hp1 HG01192.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.222+13952_222+1395 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440614 | |||||
| chr6:17440614
|
G | GGTGTGT | 4 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0002g0021others(1): Show | 4 | HG02027.hp2 HG02083.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+13950_222+1395 others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440614 | |||||
| chr6:17440614
|
G | GT | 113 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(110): Show | 113 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.222+13924_222+1392 others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440614 | ||||||
| chr6:17440614
|
G | T | 8 | a0001c0001t0001g0067a0001c0002t0001g0130a0001c0002t0001g0132others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+13924G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440614 | ||||||
| chr6:17440667
|
G | A | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+13977G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440667 | ||||||
| chr6:17440719
|
A | G | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+14029A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440719 | ||||||
| chr6:17440726
|
T | C | 6 | a0001c0002t0001g0058a0001c0002t0001g0090a0001c0008t0001g0057others(3): Show | 6 | HG00642.hp1 HG01243.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+14036T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440726 | ||||||
| chr6:17440751
|
G | A | 1 | a0001c0009t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.222+14061G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440751 | ||||||
| chr6:17440777
|
C | T | 1 | a0001c0009t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.222+14087C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440777 | ||||||
| chr6:17440818
|
A | T | 1 | a0001c0001t0001g0004 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.222+14128A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440818 | ||||||
| chr6:17440882
|
C | G | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+14192C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440882 | ||||||
| chr6:17440976
|
C | T | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+14286C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440976 | ||||||
| chr6:17441005
|
CT | C | 5 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0002g0199others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+14321delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17441005 | |||||
| chr6:17441170
|
T | A | 1 | a0001c0001t0001g0004 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.222+14480T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441170 | ||||||
| chr6:17441171
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+14481G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441171 | ||||||
| chr6:17441188
|
T | C | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+14498T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441188 | ||||||
| chr6:17441546
|
A | C | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+14856A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441546 | ||||||
| chr6:17441672
|
A | G | 1 | a0001c0002t0001g0071 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.222+14982A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441672 | ||||||
| chr6:17441688
|
T | C | 1 | a0001c0001t0002g0030 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.222+14998T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441688 | ||||||
| chr6:17441733
|
C | T | 2 | a0001c0002t0001g0058a0001c0008t0001g0057 | 2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.222+15043C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441733 | ||||||
| chr6:17441741
|
T | C | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+15051T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441741 | ||||||
| chr6:17441828
|
G | A | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+15138G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441828 | ||||||
| chr6:17441874
|
T | G | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+15184T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441874 | ||||||
| chr6:17441959
|
A | G | 138 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(135): Show | 138 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.222+15269A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441959 | ||||||
| chr6:17442095
|
A | G | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+15405A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17442095 | ||||||
| chr6:17442152
|
A | C | 1 | a0001c0002t0001g0108 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.222+15462A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17442152 | ||||||
| chr6:17442407
|
C | T | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+15717C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17442407 | ||||||
| chr6:17442654
|
A | G | 139 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(136): Show | 139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+15964A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17442654 | ||||||
| chr6:17442723
|
A | AT | 97 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(94): Show | 97 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.222+16045dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17442723 | |||||
| chr6:17442723
|
A | ATT | 40 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(37): Show | 40 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.222+16044_222+1604 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17442723 | |||||
| chr6:17442866
|
C | T | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.222+16176C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17442866 | ||||||
| chr6:17442867
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+16177G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17442867 | ||||||
| chr6:17443112
|
C | T | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222+16422C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443112 | ||||||
| chr6:17443145
|
G | A | 2 | a0001c0002t0001g0132a0001c0003t0002g0131 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.222+16455G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443145 | ||||||
| chr6:17443155
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.222+16465A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443155 | ||||||
| chr6:17443209
|
G | A | 13 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(10): Show | 13 | HG00735.hp2 HG01167.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.222+16519G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443209 | ||||||
| chr6:17443394
|
C | G | 106 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(103): Show | 106 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.222+16704C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443394 | ||||||
| chr6:17443521
|
G | A | 7 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(4): Show | 7 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+16831G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443521 | ||||||
| chr6:17443574
|
G | GACAC | 9 | a0001c0001t0001g0099a0001c0002t0001g0100a0001c0002t0002g0073others(6): Show | 9 | HG01106.hp2 HG01361.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+16901_222+1690 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17443574 | |||||
| chr6:17443574
|
G | GACACAC | 77 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(74): Show | 77 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.222+16899_222+1690 others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17443574 | |||||
| chr6:17443574
|
G | GACACACA others(1): Show |
50 | a0001c0001t0001g0034a0001c0001t0001g0074a0001c0001t0001g0075others(47): Show | 50 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.222+16897_222+1690 others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17443574 | |||||
| chr6:17443595
|
G | T | 1 | a0001c0001t0001g0007 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.222+16905G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443595 | ||||||
| chr6:17443864
|
T | C | 138 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(135): Show | 138 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.222+17174T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443864 | ||||||
| chr6:17443874
|
T | C | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.222+17184T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443874 | ||||||
| chr6:17443943
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.222+17253G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443943 | ||||||
| chr6:17443945
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.222+17255G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443945 | ||||||
| chr6:17444020
|
G | C | 1 | a0001c0002t0001g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.222+17330G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444020 | ||||||
| chr6:17444072
|
A | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222+17382A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444072 | ||||||
| chr6:17444097
|
A | G | 138 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(135): Show | 138 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.222+17407A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444097 | ||||||
| chr6:17444234
|
C | T | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+17544C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444234 | ||||||
| chr6:17444377
|
G | A | 1 | a0001c0011t0002g0081 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.222+17687G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444377 | ||||||
| chr6:17444429
|
G | A | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+17739G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444429 | ||||||
| chr6:17444510
|
T | C | 4 | a0001c0001t0002g0152a0001c0002t0001g0188a0001c0002t0001g0189others(1): Show | 4 | HG00741.hp2 HG01516.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+17820T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444510 | ||||||
| chr6:17444618
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0002g0105 | 2 | HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.222+17928C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444618 | ||||||
| chr6:17444639
|
C | CA | 111 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0034others(108): Show | 111 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.222+17968dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444639 | |||||
| chr6:17444639
|
C | CAA | 5 | a0001c0001t0001g0124a0001c0001t0001g0140a0001c0001t0001g0196others(2): Show | 5 | HG01255.hp1 HG01978.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+17967_222+1796 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444639 | |||||
| chr6:17444639
|
CA | C | 7 | a0001c0001t0001g0069a0001c0001t0002g0102a0001c0002t0001g0144others(4): Show | 7 | HG01496.hp1 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+17968delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444639 | |||||
| chr6:17444655
|
A | AG | 2 | a0001c0002t0001g0058a0001c0008t0001g0057 | 2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.222+17965_222+1796 others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444655 | ||||||
| chr6:17444674
|
G | T | 115 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(112): Show | 115 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.222+17984G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444674 | ||||||
| chr6:17444740
|
A | T | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222+18050A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444740 | ||||||
| chr6:17444804
|
C | A | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222+18114C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444804 | ||||||
| chr6:17444804
|
C | CCA | 25 | a0001c0001t0001g0048a0001c0001t0001g0068a0001c0001t0001g0074others(22): Show | 25 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.222+18153_223-1815 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | |||||
| chr6:17444804
|
C | CCACA | 13 | a0001c0001t0001g0103a0001c0001t0001g0123a0001c0001t0001g0124others(10): Show | 13 | HG01978.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.222+18151_223-1815 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | |||||
| chr6:17444804
|
C | CCACACA | 41 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0095others(38): Show | 41 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.222+18149_223-1815 others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | |||||
| chr6:17444804
|
C | CCACACAC others(1): Show |
22 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0142others(19): Show | 22 | HG01516.hp1 HG01975.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.222+18147_223-1815 others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | |||||
| chr6:17444804
|
C | CCACACAC others(3): Show |
6 | a0001c0001t0002g0126a0001c0001t0002g0162a0001c0002t0002g0135others(3): Show | 6 | HG01106.hp2 HG01981.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+18145_223-1815 others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | |||||
| chr6:17444804
|
C | CCACACAC others(5): Show |
2 | a0001c0001t0002g0050a0001c0002t0001g0198 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.222+18143_223-1815 others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | |||||
| chr6:17444804
|
CCA | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.222+18153_223-1815 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | |||||
| chr6:17444804
|
CCACA | C | 4 | a0001c0002t0001g0002a0001c0003t0002g0060a0001c0003t0002g0064others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+18151_223-1815 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | |||||
| chr6:17444804
|
CCACACA | C | 10 | a0001c0001t0001g0099a0001c0002t0001g0058a0001c0002t0001g0072others(7): Show | 10 | HG00642.hp1 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.222+18149_223-1815 others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | |||||
| chr6:17444804
|
CCACACAC others(7): Show |
C | 1 | a0001c0002t0001g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.222+18141_223-1815 others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | |||||
| chr6:17444804
|
CCACACAC others(9): Show |
C | 1 | a0001c0002t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.222+18139_223-1815 others(20): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | |||||
| chr6:17444911
|
C | T | 2 | a0002c0004t0002g0077a0002c0004t0002g0079 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.223-18085C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444911 | ||||||
| chr6:17444977
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.223-18019A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444977 | ||||||
| chr6:17444994
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.223-18002T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444994 | ||||||
| chr6:17445010
|
T | A | 98 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(95): Show | 98 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.223-17986T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445010 | ||||||
| chr6:17445021
|
T | C | 115 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(112): Show | 115 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.223-17975T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445021 | ||||||
| chr6:17445273
|
G | A | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-17723G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445273 | ||||||
| chr6:17445354
|
A | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-17642A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445354 | ||||||
| chr6:17445491
|
C | A | 1 | a0001c0002t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.223-17505C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445491 | ||||||
| chr6:17445496
|
C | T | 100 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(97): Show | 100 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.223-17500C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445496 | ||||||
| chr6:17445550
|
G | A | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-17446G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445550 | ||||||
| chr6:17445551
|
A | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-17445A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445551 | ||||||
| chr6:17445596
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.223-17400G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445596 | ||||||
| chr6:17445757
|
C | T | 4 | a0001c0001t0001g0069a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 4 | HG02486.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-17239C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445757 | ||||||
| chr6:17445850
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.223-17146G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445850 | ||||||
| chr6:17446032
|
C | T | 121 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(118): Show | 121 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.223-16964C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446032 | ||||||
| chr6:17446196
|
C | G | 8 | a0001c0002t0001g0002a0001c0002t0001g0058a0001c0002t0001g0090others(5): Show | 8 | HG00642.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-16800C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446196 | ||||||
| chr6:17446212
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.223-16784A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446212 | ||||||
| chr6:17446292
|
G | A | 98 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(95): Show | 98 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.223-16704G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446292 | ||||||
| chr6:17446353
|
C | T | 1 | a0001c0002t0001g0138 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.223-16643C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446353 | ||||||
| chr6:17446367
|
A | T | 109 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(106): Show | 109 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.223-16629A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446367 | ||||||
| chr6:17446425
|
G | T | 1 | a0003c0007t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.223-16571G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446425 | ||||||
| chr6:17446433
|
A | G | 24 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(21): Show | 24 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.223-16563A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446433 | ||||||
| chr6:17446451
|
T | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0022others(2): Show | 5 | HG02027.hp2 HG02083.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-16545T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446451 | ||||||
| chr6:17446551
|
T | C | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051 | 3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.223-16445T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446551 | ||||||
| chr6:17446569
|
G | T | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-16427G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446569 | ||||||
| chr6:17446582
|
T | C | 6 | a0001c0002t0001g0058a0001c0002t0001g0090a0001c0008t0001g0057others(3): Show | 6 | HG00642.hp1 HG01243.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.223-16414T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446582 | ||||||
| chr6:17446584
|
T | C | 2 | a0001c0002t0001g0191a0001c0002t0001g0192 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.223-16412T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446584 | ||||||
| chr6:17446594
|
T | C | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051 | 3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.223-16402T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446594 | ||||||
| chr6:17446610
|
C | T | 3 | a0001c0001t0001g0099a0001c0002t0001g0100a0004c0010t0002g0061 | 3 | HG01255.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-16386C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446610 | ||||||
| chr6:17446831
|
G | A | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-16165G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446831 | ||||||
| chr6:17446864
|
G | A | 98 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(95): Show | 98 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.223-16132G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446864 | ||||||
| chr6:17446904
|
C | T | 15 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(12): Show | 15 | HG00735.hp2 HG01167.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.223-16092C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446904 | ||||||
| chr6:17446975
|
G | A | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-16021G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446975 | ||||||
| chr6:17447020
|
G | A | 111 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(108): Show | 111 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.223-15976G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17447020 | ||||||
| chr6:17447034
|
A | T | 132 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(129): Show | 132 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.223-15962A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17447034 | ||||||
| chr6:17447175
|
TA | T | 128 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(125): Show | 128 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.223-15803delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17447175 | |||||
| chr6:17447228
|
C | G | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-15768C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17447228 | ||||||
| chr6:17447504
|
A | G | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051 | 3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.223-15492A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17447504 | ||||||
| chr6:17447754
|
T | C | 1 | a0001c0002t0006g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.223-15242T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17447754 | ||||||
| chr6:17447784
|
T | C | 1 | a0001c0009t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.223-15212T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17447784 | ||||||
| chr6:17448057
|
A | G | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051 | 3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.223-14939A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448057 | ||||||
| chr6:17448072
|
C | G | 131 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(128): Show | 131 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.223-14924C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448072 | ||||||
| chr6:17448149
|
C | T | 3 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0002g0131 | 3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.223-14847C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448149 | ||||||
| chr6:17448346
|
T | C | 1 | a0001c0002t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.223-14650T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448346 | ||||||
| chr6:17448679
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.223-14317T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448679 | ||||||
| chr6:17448712
|
C | T | 31 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(28): Show | 31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-14284C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448712 | ||||||
| chr6:17448731
|
G | A | 1 | a0001c0009t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223-14265G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448731 | ||||||
| chr6:17448768
|
CT | C | 107 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0048others(104): Show | 107 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.223-14215delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17448768 | |||||
| chr6:17448825
|
G | C | 31 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(28): Show | 31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-14171G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448825 | ||||||
| chr6:17448841
|
A | C | 1 | a0001c0009t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223-14155A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448841 | ||||||
| chr6:17448860
|
C | G | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-14136C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448860 | ||||||
| chr6:17448892
|
C | G | 131 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(128): Show | 131 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.223-14104C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448892 | ||||||
| chr6:17449053
|
C | T | 31 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(28): Show | 31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-13943C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449053 | ||||||
| chr6:17449057
|
C | A | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(7): Show | 10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-13939C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449057 | ||||||
| chr6:17449413
|
A | T | 17 | a0001c0001t0001g0053a0001c0001t0001g0074a0001c0001t0001g0075others(14): Show | 17 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.223-13583A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449413 | ||||||
| chr6:17449416
|
T | A | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-13580T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449416 | ||||||
| chr6:17449449
|
C | T | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-13547C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449449 | ||||||
| chr6:17449516
|
C | T | 6 | a0001c0002t0001g0058a0001c0002t0001g0090a0001c0008t0001g0057others(3): Show | 6 | HG00642.hp1 HG01243.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.223-13480C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449516 | ||||||
| chr6:17449545
|
TA | T | 4 | a0001c0002t0001g0090a0003c0007t0001g0059a0003c0007t0001g0066others(1): Show | 4 | HG01243.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-13450delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449545 | ||||||
| chr6:17449611
|
G | A | 100 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(97): Show | 100 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.223-13385G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449611 | ||||||
| chr6:17449664
|
C | G | 1 | a0001c0002t0001g0128 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.223-13332C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449664 | ||||||
| chr6:17450054
|
C | A | 1 | a0001c0002t0001g0128 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.223-12942C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17450054 | ||||||
| chr6:17450055
|
CT | C | 5 | a0001c0001t0001g0025a0001c0001t0002g0163a0001c0002t0002g0160others(2): Show | 5 | HG03017.hp2 HG03041.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-12927delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17450055 | |||||
| chr6:17450104
|
T | A | 21 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(18): Show | 21 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.223-12892T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17450104 | ||||||
| chr6:17450134
|
C | T | 1 | a0002c0004t0001g0089 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.223-12862C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17450134 | ||||||
| chr6:17450244
|
G | T | 31 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(28): Show | 31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-12752G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17450244 | ||||||
| chr6:17450496
|
G | C | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-12500G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17450496 | ||||||
| chr6:17450885
|
G | A | 2 | a0001c0002t0001g0109a0001c0002t0001g0164 | 2 | HG02027.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.223-12111G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17450885 | ||||||
| chr6:17451221
|
ATCT | A | 14 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0002t0001g0144others(11): Show | 14 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.223-11771_223-1176 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17451221 | |||||
| chr6:17451231
|
CA | C | 112 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(109): Show | 112 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.223-11753delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17451231 | |||||
| chr6:17451232
|
A | T | 1 | a0002c0004t0001g0089 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.223-11764A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451232 | ||||||
| chr6:17451241
|
A | T | 5 | a0001c0001t0001g0054a0001c0001t0002g0055a0001c0002t0001g0058others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-11755A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451241 | ||||||
| chr6:17451242
|
AAT | A | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-11752_223-1175 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17451242 | |||||
| chr6:17451412
|
C | T | 1 | a0002c0012t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.223-11584C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451412 | ||||||
| chr6:17451569
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0002g0055 | 3 | HG01168.hp1 HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.223-11427G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451569 | ||||||
| chr6:17451667
|
G | A | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-11329G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451667 | ||||||
| chr6:17451819
|
C | G | 2 | a0001c0002t0001g0191a0001c0002t0001g0192 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.223-11177C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451819 | ||||||
| chr6:17451850
|
CT | C | 31 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(28): Show | 31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-11145delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451850 | ||||||
| chr6:17452111
|
G | A | 31 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(28): Show | 31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-10885G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452111 | ||||||
| chr6:17452154
|
T | G | 31 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(28): Show | 31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-10842T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452154 | ||||||
| chr6:17452345
|
C | T | 1 | a0001c0009t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223-10651C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452345 | ||||||
| chr6:17452374
|
C | T | 1 | a0002c0004t0001g0089 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.223-10622C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452374 | ||||||
| chr6:17452469
|
G | T | 131 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(128): Show | 131 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.223-10527G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452469 | ||||||
| chr6:17452508
|
G | A | 37 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(34): Show | 37 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.223-10488G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452508 | ||||||
| chr6:17452526
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.223-10470C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452526 | ||||||
| chr6:17452609
|
A | T | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-10387A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452609 | ||||||
| chr6:17452680
|
T | G | 31 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(28): Show | 31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-10316T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452680 | ||||||
| chr6:17452692
|
C | G | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-10304C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452692 | ||||||
| chr6:17452730
|
G | A | 32 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(29): Show | 32 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.223-10266G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452730 | ||||||
| chr6:17452730
|
G | C | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-10266G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452730 | ||||||
| chr6:17452770
|
GTTTCACT others(4): Show |
G | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051 | 3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.223-10221_223-1021 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17452770 | |||||
| chr6:17452854
|
G | A | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-10142G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452854 | ||||||
| chr6:17453266
|
AAC | A | 2 | a0001c0001t0002g0163a0001c0002t0002g0135 | 2 | HG01981.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.223-9727_223-9726d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17453266 | |||||
| chr6:17453552
|
C | T | 32 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(29): Show | 32 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.223-9444C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453552 | ||||||
| chr6:17453603
|
A | C | 17 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(14): Show | 17 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.223-9393A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453603 | ||||||
| chr6:17453705
|
C | T | 2 | a0001c0002t0001g0093a0001c0002t0001g0094 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.223-9291C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453705 | ||||||
| chr6:17453793
|
G | A | 1 | a0001c0002t0002g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.223-9203G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453793 | ||||||
| chr6:17453839
|
C | T | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-9157C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453839 | ||||||
| chr6:17453884
|
CTCTT | C | 2 | a0001c0002t0001g0062a0001c0002t0002g0073 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.223-9108_223-9105d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17453884 | |||||
| chr6:17453901
|
CT | C | 97 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(94): Show | 97 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.223-9077delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17453901 | |||||
| chr6:17453902
|
T | TTTC | 31 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(28): Show | 31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-9092_223-9091i others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17453902 | |||||
| chr6:17453906
|
T | C | 4 | a0001c0001t0001g0085a0001c0003t0002g0060a0001c0003t0002g0064others(1): Show | 4 | HG02109.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-9090T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453906 | ||||||
| chr6:17453919
|
T | C | 1 | a0001c0011t0002g0081 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.223-9077T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453919 | ||||||
| chr6:17453941
|
A | G | 121 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(118): Show | 121 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.223-9055A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453941 | ||||||
| chr6:17453990
|
CCCTCCCA others(6): Show |
C | 16 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(13): Show | 16 | HG00735.hp2 HG01167.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.223-8973_223-8961d others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17453990 | |||||
| chr6:17454419
|
C | A | 33 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(30): Show | 33 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.223-8577C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454419 | ||||||
| chr6:17454545
|
C | T | 3 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0002g0131 | 3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.223-8451C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454545 | ||||||
| chr6:17454614
|
T | C | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.223-8382T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454614 | ||||||
| chr6:17454618
|
G | T | 33 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(30): Show | 33 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.223-8378G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454618 | ||||||
| chr6:17454920
|
C | T | 2 | a0001c0002t0001g0193a0006c0016t0001g0194 | 2 | HG03831.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.223-8076C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454920 | ||||||
| chr6:17454921
|
G | A | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(7): Show | 10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-8075G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454921 | ||||||
| chr6:17454977
|
T | C | 8 | a0001c0002t0001g0002a0001c0002t0001g0058a0001c0002t0001g0090others(5): Show | 8 | HG00642.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-8019T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454977 | ||||||
| chr6:17454980
|
A | G | 33 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(30): Show | 33 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.223-8016A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454980 | ||||||
| chr6:17455034
|
C | T | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-7962C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455034 | ||||||
| chr6:17455283
|
G | GA | 5 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0022others(2): Show | 5 | HG02027.hp2 HG02083.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-7701dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17455283 | |||||
| chr6:17455283
|
GA | G | 110 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(107): Show | 110 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.223-7701delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17455283 | |||||
| chr6:17455314
|
G | A | 3 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0002g0131 | 3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.223-7682G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455314 | ||||||
| chr6:17455600
|
A | G | 17 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(14): Show | 17 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.223-7396A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455600 | ||||||
| chr6:17455677
|
A | G | 22 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(19): Show | 22 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.223-7319A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455677 | ||||||
| chr6:17455680
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.223-7316C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455680 | ||||||
| chr6:17455725
|
T | C | 142 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(139): Show | 142 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.223-7271T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455725 | ||||||
| chr6:17455814
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.223-7182C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455814 | ||||||
| chr6:17455819
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.223-7177G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455819 | ||||||
| chr6:17455824
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.223-7172C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455824 | ||||||
| chr6:17455831
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.223-7165A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455831 | ||||||
| chr6:17455931
|
A | G | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.223-7065A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455931 | ||||||
| chr6:17455958
|
T | TA | 2 | a0001c0002t0001g0125a0001c0002t0002g0129 | 2 | HG01167.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.223-7037dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17455958 | |||||
| chr6:17455999
|
C | T | 1 | a0001c0009t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223-6997C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455999 | ||||||
| chr6:17456019
|
A | T | 3 | a0001c0002t0001g0058a0001c0002t0001g0090a0001c0008t0001g0057 | 3 | HG00642.hp1 HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.223-6977A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456019 | ||||||
| chr6:17456046
|
G | A | 5 | a0001c0002t0001g0002a0001c0002t0001g0058a0001c0002t0001g0090others(2): Show | 5 | HG00642.hp1 HG01243.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-6950G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456046 | ||||||
| chr6:17456186
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.223-6810G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456186 | ||||||
| chr6:17456269
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0078 | 2 | HG01167.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.223-6727C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456269 | ||||||
| chr6:17456361
|
G | C | 18 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(15): Show | 18 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.223-6635G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456361 | ||||||
| chr6:17456463
|
T | A | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-6533T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456463 | ||||||
| chr6:17456504
|
G | C | 9 | a0001c0001t0002g0102a0001c0002t0001g0108a0001c0002t0002g0111others(6): Show | 9 | HG01496.hp1 HG01928.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-6492G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456504 | ||||||
| chr6:17456584
|
C | T | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-6412C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456584 | ||||||
| chr6:17456595
|
C | T | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-6401C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456595 | ||||||
| chr6:17456669
|
T | C | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-6327T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456669 | ||||||
| chr6:17456670
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.223-6326T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456670 | ||||||
| chr6:17456825
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.223-6171C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456825 | ||||||
| chr6:17456826
|
C | A | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-6170C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456826 | ||||||
| chr6:17456876
|
T | G | 141 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(138): Show | 141 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.223-6120T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456876 | ||||||
| chr6:17456966
|
G | C | 1 | a0001c0001t0001g0016 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.223-6030G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456966 | ||||||
| chr6:17457195
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.223-5801C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457195 | ||||||
| chr6:17457318
|
G | A | 3 | a0001c0002t0001g0107a0001c0002t0001g0136a0001c0002t0001g0184 | 3 | HG00099.hp2 HG01175.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.223-5678G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457318 | ||||||
| chr6:17457399
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.223-5597C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457399 | ||||||
| chr6:17457440
|
G | A | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-5556G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457440 | ||||||
| chr6:17457473
|
A | T | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-5523A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457473 | ||||||
| chr6:17457547
|
G | T | 1 | a0001c0009t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223-5449G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457547 | ||||||
| chr6:17457637
|
G | C | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-5359G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457637 | ||||||
| chr6:17457677
|
C | A | 3 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0002g0131 | 3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.223-5319C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457677 | ||||||
| chr6:17457906
|
A | G | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.223-5090A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457906 | ||||||
| chr6:17458030
|
C | G | 6 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0002g0055others(3): Show | 6 | HG01168.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-4966C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458030 | ||||||
| chr6:17458128
|
T | G | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.223-4868T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458128 | ||||||
| chr6:17458234
|
A | G | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-4762A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458234 | ||||||
| chr6:17458349
|
A | G | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-4647A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458349 | ||||||
| chr6:17458359
|
A | G | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-4637A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458359 | ||||||
| chr6:17458513
|
A | G | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(7): Show | 10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-4483A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458513 | ||||||
| chr6:17458621
|
T | C | 1 | a0002c0004t0001g0089 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.223-4375T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458621 | ||||||
| chr6:17458722
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.223-4274C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458722 | ||||||
| chr6:17458814
|
T | C | 36 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(33): Show | 36 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.223-4182T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458814 | ||||||
| chr6:17458885
|
G | A | 36 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(33): Show | 36 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.223-4111G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458885 | ||||||
| chr6:17458886
|
C | CA | 13 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0002g0137others(10): Show | 13 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.223-4095dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17458886 | |||||
| chr6:17458886
|
C | CAA | 11 | a0001c0002t0001g0002a0001c0002t0001g0058a0001c0002t0001g0090others(8): Show | 11 | HG00642.hp1 HG01243.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-4096_223-4095d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17458886 | |||||
| chr6:17458886
|
C | CAAA | 25 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(22): Show | 25 | HG00735.hp2 HG01167.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.223-4097_223-4095d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17458886 | |||||
| chr6:17459055
|
C | A | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.223-3941C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459055 | ||||||
| chr6:17459099
|
T | G | 9 | a0001c0002t0001g0002a0001c0002t0001g0058a0001c0002t0001g0090others(6): Show | 9 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-3897T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459099 | ||||||
| chr6:17459214
|
C | T | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-3782C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459214 | ||||||
| chr6:17459302
|
T | C | 3 | a0001c0001t0002g0050a0001c0009t0001g0014a0001c0014t0008g0015 | 3 | HG01361.hp2 HG02486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.223-3694T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459302 | ||||||
| chr6:17459486
|
G | A | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-3510G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459486 | ||||||
| chr6:17459522
|
G | T | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-3474G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459522 | ||||||
| chr6:17459739
|
AATG | A | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(7): Show | 10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-3254_223-3252d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17459739 | |||||
| chr6:17459815
|
G | A | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-3181G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459815 | ||||||
| chr6:17459850
|
C | T | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-3146C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459850 | ||||||
| chr6:17459930
|
G | A | 98 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(95): Show | 98 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.223-3066G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459930 | ||||||
| chr6:17459934
|
C | T | 100 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(97): Show | 100 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.223-3062C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459934 | ||||||
| chr6:17459945
|
C | T | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-3051C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459945 | ||||||
| chr6:17459994
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.223-3002T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459994 | ||||||
| chr6:17460026
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.223-2970G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460026 | ||||||
| chr6:17460150
|
T | C | 1 | a0001c0009t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223-2846T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460150 | ||||||
| chr6:17460153
|
C | T | 28 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(25): Show | 28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-2843C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460153 | ||||||
| chr6:17460168
|
C | T | 95 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(92): Show | 95 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.223-2828C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460168 | ||||||
| chr6:17460284
|
C | CTT | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-2711_223-2710i others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17460284 | |||||
| chr6:17460320
|
G | A | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-2676G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460320 | ||||||
| chr6:17460617
|
C | G | 18 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(15): Show | 18 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.223-2379C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460617 | ||||||
| chr6:17460620
|
G | A | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-2376G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460620 | ||||||
| chr6:17460738
|
C | T | 7 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(4): Show | 7 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-2258C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460738 | ||||||
| chr6:17460847
|
A | T | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-2149A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460847 | ||||||
| chr6:17460928
|
G | A | 6 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0002g0055others(3): Show | 6 | HG01168.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-2068G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460928 | ||||||
| chr6:17460994
|
C | T | 136 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(133): Show | 136 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.223-2002C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460994 | ||||||
| chr6:17461005
|
C | T | 2 | a0001c0002t0001g0193a0006c0016t0001g0194 | 2 | HG03831.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.223-1991C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461005 | ||||||
| chr6:17461013
|
G | A | 1 | a0001c0002t0002g0167 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.223-1983G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461013 | ||||||
| chr6:17461188
|
CAA | C | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-1798_223-1797d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461188 | |||||
| chr6:17461191
|
A | C | 2 | a0001c0001t0002g0031a0001c0002t0001g0134 | 2 | HG02071.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.223-1805A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461191 | ||||||
| chr6:17461199
|
A | C | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(7): Show | 10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-1797A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461199 | ||||||
| chr6:17461218
|
C | G | 26 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(23): Show | 26 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.223-1778C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461218 | ||||||
| chr6:17461218
|
C | T | 1 | a0001c0002t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.223-1778C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461218 | ||||||
| chr6:17461218
|
CT | C | 108 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0052others(105): Show | 108 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.223-1767delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461218 | |||||
| chr6:17461219
|
T | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.223-1777T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461219 | ||||||
| chr6:17461238
|
G | T | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(7): Show | 10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-1758G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461238 | ||||||
| chr6:17461239
|
A | T | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(7): Show | 10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-1757A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461239 | ||||||
| chr6:17461240
|
G | A | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(7): Show | 10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-1756G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461240 | ||||||
| chr6:17461242
|
C | T | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.223-1754C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461242 | ||||||
| chr6:17461428
|
T | G | 28 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(25): Show | 28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-1568T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461428 | ||||||
| chr6:17461476
|
T | C | 38 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0074others(35): Show | 38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-1520T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461476 | ||||||
| chr6:17461638
|
G | A | 97 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(94): Show | 97 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.223-1358G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461638 | ||||||
| chr6:17461709
|
A | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0040 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.223-1287A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461709 | ||||||
| chr6:17461737
|
G | A | 134 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(131): Show | 134 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.223-1259G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461737 | ||||||
| chr6:17461776
|
A | T | 28 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(25): Show | 28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-1220A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461776 | ||||||
| chr6:17461793
|
C | T | 5 | a0001c0001t0001g0099a0001c0002t0001g0100a0001c0002t0001g0130others(2): Show | 5 | HG03130.hp2 HG03195.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-1203C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461793 | ||||||
| chr6:17461795
|
A | G | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.223-1201A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461795 | ||||||
| chr6:17461803
|
G | T | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.223-1193G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461803 | ||||||
| chr6:17461809
|
T | G | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.223-1187T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461809 | ||||||
| chr6:17461861
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.223-1135C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461861 | ||||||
| chr6:17461882
|
A | C | 97 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0048others(94): Show | 97 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.223-1114A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461882 | ||||||
| chr6:17461917
|
T | C | 28 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(25): Show | 28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-1079T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461917 | ||||||
| chr6:17461950
|
A | G | 134 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(131): Show | 134 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.223-1046A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461950 | ||||||
| chr6:17461950
|
A | T | 3 | a0001c0001t0001g0099a0001c0001t0002g0050a0001c0002t0001g0100 | 3 | HG02486.hp2 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-1046A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461950 | ||||||
| chr6:17461954
|
T | C | 1 | a0001c0001t0002g0169 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.223-1042T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461954 | ||||||
| chr6:17461976
|
G | C | 27 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(24): Show | 27 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.223-1020G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461976 | ||||||
| chr6:17461977
|
G | A | 1 | a0001c0003t0002g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.223-1019G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461977 | ||||||
| chr6:17461992
|
C | CA | 19 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0018others(16): Show | 19 | HG00642.hp2 HG00735.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.223-973dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0002g0172a0001c0006t0001g0155a0002c0005t0001g0003others(1): Show | 4 | HG02135.hp1 HG02135.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-982_223-973dup others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0002t0001g0112others(1): Show | 4 | HG02735.hp1 HG02976.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-985_223-973dup others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0103a0001c0001t0001g0123 | 2 | HG03130.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.223-986_223-973dup others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(8): Show |
10 | a0001c0001t0002g0126a0001c0001t0002g0163a0001c0001t0002g0175others(7): Show | 10 | HG01243.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-987_223-973dup others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(9): Show |
5 | a0001c0001t0001g0165a0001c0001t0002g0206a0001c0002t0001g0093others(2): Show | 5 | HG00609.hp1 HG01943.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-988_223-973dup others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(10): Show |
8 | a0001c0001t0001g0174a0001c0001t0002g0049a0001c0001t0002g0162others(5): Show | 8 | HG00438.hp2 HG01517.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-989_223-973dup others(17): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(11): Show |
4 | a0001c0001t0001g0143a0001c0001t0002g0030a0001c0001t0002g0150others(1): Show | 4 | HG01168.hp2 NA18990.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-990_223-973dup others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0052a0001c0001t0001g0142 | 2 | HG01891.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.223-991_223-973dup others(19): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0140 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.223-992_223-973dup others(20): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.223-993_223-973dup others(21): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(15): Show |
3 | a0001c0001t0001g0053a0001c0001t0002g0105a0001c0002t0001g0072 | 3 | HG01952.hp2 HG02896.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.223-994_223-973dup others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(16): Show |
1 | a0001c0002t0001g0071 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.223-995_223-973dup others(23): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(19): Show |
1 | a0001c0002t0001g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.223-998_223-973dup others(26): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
C | CAAAAAAA others(31): Show |
1 | a0001c0008t0001g0204 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.223-973_223-972ins others(38): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
CA | C | 10 | a0001c0001t0002g0121a0001c0001t0002g0158a0001c0001t0002g0171others(7): Show | 10 | HG01261.hp1 HG01928.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-973delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
CAA | C | 5 | a0001c0001t0001g0099a0001c0001t0002g0147a0001c0001t0002g0169others(2): Show | 5 | HG01255.hp2 HG01261.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-974_223-973del others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
CAAAAA | C | 8 | a0001c0001t0001g0069a0001c0001t0001g0159a0001c0001t0001g0196others(5): Show | 8 | HG00741.hp2 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.223-977_223-973del others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
CAAAAAAA others(1): Show |
C | 25 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0078others(22): Show | 25 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.223-980_223-973del others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
CAAAAAAA others(2): Show |
C | 10 | a0001c0001t0001g0076a0001c0001t0001g0179a0001c0001t0001g0180others(7): Show | 10 | HG02083.hp2 HG02897.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-981_223-973del others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0002g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.223-984_223-973del others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
CAAAAAAA others(7): Show |
C | 1 | a0003c0007t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.223-986_223-973del others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
CAAAAAAA others(10): Show |
C | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-989_223-973del others(17): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17461992
|
CAAAAAAA others(11): Show |
C | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-990_223-973del others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | |||||
| chr6:17462085
|
A | T | 28 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(25): Show | 28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-911A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462085 | ||||||
| chr6:17462089
|
A | G | 28 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(25): Show | 28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-907A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462089 | ||||||
| chr6:17462114
|
T | C | 28 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(25): Show | 28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-882T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462114 | ||||||
| chr6:17462214
|
G | C | 2 | a0001c0002t0001g0093a0001c0002t0001g0094 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.223-782G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462214 | ||||||
| chr6:17462243
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.223-753C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462243 | ||||||
| chr6:17462302
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.223-694G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462302 | ||||||
| chr6:17462418
|
CAT | C | 5 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0002g0199others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-577_223-576del others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462418 | ||||||
| chr6:17462568
|
GC | G | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(7): Show | 10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-424delC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17462568 | |||||
| chr6:17462815
|
G | A | 28 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(25): Show | 28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-181G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462815 | ||||||
| chr6:17463250
|
C | G | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.300+177C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463250 | ||||||
| chr6:17463268
|
G | GT | 15 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(12): Show | 15 | HG00735.hp2 HG01167.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.300+207dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17463268 | |||||
| chr6:17463268
|
G | GTT | 10 | a0001c0002t0001g0002a0001c0002t0001g0058a0001c0002t0001g0090others(7): Show | 10 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+206_300+207dup others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17463268 | |||||
| chr6:17463295
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.300+222C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463295 | ||||||
| chr6:17463319
|
G | A | 18 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(15): Show | 18 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.300+246G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463319 | ||||||
| chr6:17463362
|
C | G | 1 | a0001c0002t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.300+289C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463362 | ||||||
| chr6:17463365
|
A | G | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+292A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463365 | ||||||
| chr6:17463435
|
C | T | 94 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(91): Show | 94 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.300+362C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463435 | ||||||
| chr6:17463472
|
T | A | 10 | a0001c0002t0001g0002a0001c0002t0001g0058a0001c0002t0001g0090others(7): Show | 10 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+399T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463472 | ||||||
| chr6:17463573
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.300+500C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463573 | ||||||
| chr6:17463574
|
G | A | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.300+501G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463574 | ||||||
| chr6:17463613
|
T | C | 10 | a0001c0002t0001g0002a0001c0002t0001g0058a0001c0002t0001g0090others(7): Show | 10 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+540T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463613 | ||||||
| chr6:17463698
|
C | G | 132 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(129): Show | 132 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.300+625C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463698 | ||||||
| chr6:17463816
|
A | G | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(6): Show | 9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+743A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463816 | ||||||
| chr6:17464043
|
T | C | 140 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(137): Show | 140 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.300+970T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464043 | ||||||
| chr6:17464111
|
G | A | 3 | a0001c0001t0002g0050a0001c0009t0001g0014a0001c0014t0008g0015 | 3 | HG01361.hp2 HG02486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+1038G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464111 | ||||||
| chr6:17464195
|
G | A | 3 | a0001c0002t0001g0058a0001c0002t0001g0090a0001c0008t0001g0057 | 3 | HG00642.hp1 HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.300+1122G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464195 | ||||||
| chr6:17464269
|
G | A | 1 | a0001c0003t0002g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.300+1196G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464269 | ||||||
| chr6:17464456
|
A | G | 132 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(129): Show | 132 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.300+1383A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464456 | ||||||
| chr6:17464535
|
A | G | 3 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0002g0131 | 3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.300+1462A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464535 | ||||||
| chr6:17464565
|
G | C | 134 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(131): Show | 134 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.300+1492G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464565 | ||||||
| chr6:17464574
|
T | C | 88 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(85): Show | 88 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.300+1501T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464574 | ||||||
| chr6:17464661
|
A | G | 10 | a0001c0002t0001g0002a0001c0002t0001g0058a0001c0002t0001g0090others(7): Show | 10 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+1588A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464661 | ||||||
| chr6:17464784
|
A | G | 113 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(110): Show | 113 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.300+1711A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464784 | ||||||
| chr6:17464829
|
G | A | 11 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0002g0137others(8): Show | 11 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+1756G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464829 | ||||||
| chr6:17464848
|
G | A | 2 | a0001c0002t0001g0090a0004c0010t0002g0061 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.300+1775G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464848 | ||||||
| chr6:17464867
|
G | A | 10 | a0001c0002t0001g0002a0001c0002t0001g0058a0001c0002t0001g0090others(7): Show | 10 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+1794G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464867 | ||||||
| chr6:17464884
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.300+1811G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464884 | ||||||
| chr6:17465034
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0174 | 2 | HG02071.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.300+1961A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465034 | ||||||
| chr6:17465097
|
A | G | 13 | a0001c0002t0001g0002a0001c0002t0001g0058a0001c0002t0001g0090others(10): Show | 13 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.300+2024A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465097 | ||||||
| chr6:17465268
|
T | C | 1 | a0006c0016t0001g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.300+2195T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465268 | ||||||
| chr6:17465343
|
C | A | 8 | a0001c0001t0001g0069a0001c0001t0001g0196a0001c0001t0001g0202others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+2270C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465343 | ||||||
| chr6:17465365
|
C | A | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.300+2292C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465365 | ||||||
| chr6:17465513
|
C | T | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+2440C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465513 | ||||||
| chr6:17465690
|
A | G | 6 | a0001c0001t0002g0037a0001c0002t0001g0144a0001c0002t0001g0145others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+2617A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465690 | ||||||
| chr6:17465691
|
A | G | 6 | a0001c0001t0002g0037a0001c0002t0001g0144a0001c0002t0001g0145others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+2618A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465691 | ||||||
| chr6:17465697
|
T | C | 8 | a0001c0001t0001g0069a0001c0001t0001g0196a0001c0001t0001g0202others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+2624T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465697 | ||||||
| chr6:17465732
|
C | T | 1 | a0001c0002t0001g0062 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.300+2659C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465732 | ||||||
| chr6:17465750
|
A | G | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.300+2677A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465750 | ||||||
| chr6:17465911
|
G | T | 1 | a0001c0001t0002g0121 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.300+2838G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465911 | ||||||
| chr6:17466056
|
G | A | 12 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(9): Show | 12 | HG01496.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+2983G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466056 | ||||||
| chr6:17466223
|
T | A | 9 | a0001c0001t0001g0099a0001c0001t0002g0050a0001c0002t0001g0100others(6): Show | 9 | HG02280.hp2 HG02486.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+3150T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466223 | ||||||
| chr6:17466430
|
C | A | 8 | a0001c0001t0001g0069a0001c0001t0001g0196a0001c0001t0001g0202others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+3357C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466430 | ||||||
| chr6:17466491
|
G | C | 15 | a0001c0001t0001g0099a0001c0001t0002g0037a0001c0001t0002g0050others(12): Show | 15 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.300+3418G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466491 | ||||||
| chr6:17466493
|
A | G | 6 | a0001c0001t0002g0037a0001c0002t0001g0144a0001c0002t0001g0145others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+3420A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466493 | ||||||
| chr6:17466666
|
C | T | 6 | a0001c0001t0002g0037a0001c0002t0001g0144a0001c0002t0001g0145others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+3593C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466666 | ||||||
| chr6:17466678
|
T | C | 136 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0048others(133): Show | 136 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.300+3605T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466678 | ||||||
| chr6:17466691
|
C | T | 1 | a0001c0002t0001g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.300+3618C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466691 | ||||||
| chr6:17466750
|
T | C | 1 | a0001c0001t0002g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.300+3677T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466750 | ||||||
| chr6:17466860
|
C | T | 6 | a0001c0001t0002g0037a0001c0002t0001g0144a0001c0002t0001g0145others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+3787C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466860 | ||||||
| chr6:17466928
|
A | G | 6 | a0001c0001t0002g0037a0001c0002t0001g0144a0001c0002t0001g0145others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+3855A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466928 | ||||||
| chr6:17467050
|
T | C | 1 | a0001c0001t0002g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.300+3977T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467050 | ||||||
| chr6:17467110
|
C | T | 9 | a0001c0001t0001g0099a0001c0001t0002g0050a0001c0002t0001g0100others(6): Show | 9 | HG02280.hp2 HG02486.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+4037C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467110 | ||||||
| chr6:17467112
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.300+4039C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467112 | ||||||
| chr6:17467232
|
A | G | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+4159A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467232 | ||||||
| chr6:17467533
|
T | G | 3 | a0001c0001t0001g0085a0002c0004t0001g0089a0004c0010t0002g0061 | 3 | HG00735.hp2 HG01255.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.300+4460T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467533 | ||||||
| chr6:17467611
|
C | A | 1 | a0001c0001t0002g0163 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.300+4538C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467611 | ||||||
| chr6:17467636
|
G | C | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+4563G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467636 | ||||||
| chr6:17467775
|
G | T | 3 | a0001c0001t0001g0085a0002c0004t0001g0089a0004c0010t0002g0061 | 3 | HG00735.hp2 HG01255.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.300+4702G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467775 | ||||||
| chr6:17467803
|
A | G | 1 | a0001c0002t0002g0115 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.300+4730A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467803 | ||||||
| chr6:17467815
|
A | C | 35 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0075others(32): Show | 35 | HG01109.hp2 HG01167.hp2 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.300+4742A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467815 | ||||||
| chr6:17467830
|
C | T | 5 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0002g0199others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+4757C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467830 | ||||||
| chr6:17468300
|
G | A | 3 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0002g0131 | 3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.300+5227G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17468300 | ||||||
| chr6:17468467
|
C | G | 16 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(13): Show | 16 | HG01167.hp2 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.300+5394C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17468467 | ||||||
| chr6:17468631
|
C | T | 1 | a0002c0005t0003g0170 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.300+5558C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17468631 | ||||||
| chr6:17468809
|
T | C | 6 | a0001c0001t0002g0037a0001c0002t0001g0144a0001c0002t0001g0145others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+5736T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17468809 | ||||||
| chr6:17468906
|
C | T | 1 | a0001c0014t0008g0015 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.300+5833C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17468906 | ||||||
| chr6:17469030
|
CCACCT | C | 6 | a0001c0001t0002g0037a0001c0002t0001g0144a0001c0002t0001g0145others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+5973_300+5977d others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17469030 | |||||
| chr6:17469090
|
A | G | 1 | a0001c0002t0001g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.300+6017A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469090 | ||||||
| chr6:17469270
|
C | T | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051 | 3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+6197C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469270 | ||||||
| chr6:17469285
|
T | C | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.300+6212T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469285 | ||||||
| chr6:17469416
|
C | CTGTGTGT others(1): Show |
2 | a0001c0001t0002g0126a0001c0001t0002g0175 | 2 | NA18747.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.300+6353_300+6360d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17469416 | |||||
| chr6:17469416
|
CTG | C | 4 | a0001c0001t0001g0086a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+6359_300+6360d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17469416 | |||||
| chr6:17469558
|
A | G | 5 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0002g0199others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+6485A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469558 | ||||||
| chr6:17469593
|
G | C | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.300+6520G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469593 | ||||||
| chr6:17469618
|
G | A | 3 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0002g0131 | 3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.300+6545G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469618 | ||||||
| chr6:17469624
|
A | G | 5 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+6551A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469624 | ||||||
| chr6:17469957
|
A | G | 3 | a0001c0001t0001g0099a0001c0001t0002g0050a0001c0002t0001g0100 | 3 | HG02486.hp2 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.300+6884A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469957 | ||||||
| chr6:17470183
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0002g0050a0001c0002t0001g0100 | 3 | HG02486.hp2 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.300+7110G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470183 | ||||||
| chr6:17470208
|
A | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+7135A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470208 | ||||||
| chr6:17470295
|
G | A | 3 | a0001c0001t0001g0085a0002c0004t0001g0089a0004c0010t0002g0061 | 3 | HG00735.hp2 HG01255.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.300+7222G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470295 | ||||||
| chr6:17470336
|
G | C | 7 | a0001c0001t0001g0099a0001c0001t0002g0037a0001c0001t0002g0050others(4): Show | 7 | HG02486.hp2 HG02630.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.300+7263G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470336 | ||||||
| chr6:17470406
|
T | G | 1 | a0001c0001t0002g0031 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.300+7333T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470406 | ||||||
| chr6:17470462
|
A | G | 126 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(123): Show | 126 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.300+7389A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470462 | ||||||
| chr6:17470466
|
A | T | 3 | a0001c0001t0001g0099a0001c0001t0002g0050a0001c0002t0001g0100 | 3 | HG02486.hp2 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.300+7393A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470466 | ||||||
| chr6:17470769
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.300+7696A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470769 | ||||||
| chr6:17470797
|
G | T | 2 | a0001c0002t0001g0062a0001c0002t0002g0073 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.300+7724G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470797 | ||||||
| chr6:17470840
|
T | C | 10 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+7767T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470840 | ||||||
| chr6:17471362
|
T | C | 3 | a0001c0001t0001g0085a0002c0004t0001g0089a0004c0010t0002g0061 | 3 | HG00735.hp2 HG01255.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.300+8289T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471362 | ||||||
| chr6:17471561
|
G | A | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+8488G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471561 | ||||||
| chr6:17471603
|
C | G | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+8530C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471603 | ||||||
| chr6:17471615
|
G | A | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+8542G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471615 | ||||||
| chr6:17471645
|
A | C | 1 | a0001c0003t0001g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.300+8572A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471645 | ||||||
| chr6:17471659
|
G | A | 10 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+8586G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471659 | ||||||
| chr6:17471788
|
G | A | 5 | a0001c0002t0001g0035a0001c0002t0001g0188a0001c0002t0001g0189others(2): Show | 5 | HG00741.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+8715G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471788 | ||||||
| chr6:17471830
|
CA | C | 79 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(76): Show | 79 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.300+8772delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17471830 | |||||
| chr6:17471830
|
CAA | C | 46 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(43): Show | 46 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.300+8771_300+8772d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17471830 | |||||
| chr6:17471997
|
G | A | 6 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051others(3): Show | 6 | HG01255.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+8924G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471997 | ||||||
| chr6:17472035
|
T | C | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051 | 3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+8962T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17472035 | ||||||
| chr6:17472038
|
TAATAGTG others(306): Show |
T | 126 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(123): Show | 126 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.300+8982_300+9294d others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17472038 | |||||
| chr6:17472207
|
G | A | 3 | a0001c0002t0001g0101a0001c0002t0001g0112a0001c0008t0001g0204 | 3 | HG02055.hp2 HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.300+9134G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17472207 | ||||||
| chr6:17472333
|
C | CA | 6 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0029others(3): Show | 6 | HG00438.hp1 HG02055.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+9280dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17472333 | |||||
| chr6:17472661
|
C | T | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+9588C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17472661 | ||||||
| chr6:17472872
|
T | C | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+9799T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17472872 | ||||||
| chr6:17472972
|
C | G | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.300+9899C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17472972 | ||||||
| chr6:17473023
|
T | G | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+9950T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473023 | ||||||
| chr6:17473037
|
CT | C | 19 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0075others(16): Show | 19 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.300+9977delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17473037 | |||||
| chr6:17473039
|
T | G | 10 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+9966T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473039 | ||||||
| chr6:17473253
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.300+10180G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473253 | ||||||
| chr6:17473515
|
C | T | 10 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+10442C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473515 | ||||||
| chr6:17473599
|
G | T | 1 | a0002c0004t0001g0089 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.300+10526G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473599 | ||||||
| chr6:17473696
|
T | G | 76 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(73): Show | 76 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.300+10623T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473696 | ||||||
| chr6:17473953
|
A | G | 10 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+10880A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473953 | ||||||
| chr6:17474151
|
T | A | 1 | a0001c0001t0002g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.300+11078T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474151 | ||||||
| chr6:17474184
|
TC | T | 4 | a0001c0008t0001g0051a0001c0009t0001g0012a0001c0009t0001g0014others(1): Show | 4 | HG01361.hp2 HG02486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+11112delC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474184 | ||||||
| chr6:17474185
|
C | CT | 15 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0095others(12): Show | 15 | HG00438.hp1 HG00741.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.300+11137dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474185 | |||||
| chr6:17474185
|
CT | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0068others(22): Show | 25 | HG00642.hp1 HG01071.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.300+11137delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474185 | |||||
| chr6:17474185
|
CTT | C | 84 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(81): Show | 84 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.300+11136_300+1113 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474185 | |||||
| chr6:17474185
|
CTTT | C | 12 | a0001c0001t0001g0069a0001c0001t0001g0099a0001c0001t0001g0196others(9): Show | 12 | HG00735.hp2 HG01109.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+11135_300+1113 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474185 | |||||
| chr6:17474185
|
CTTTT | C | 5 | a0001c0001t0002g0037a0001c0002t0001g0002a0001c0002t0001g0130others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+11134_300+1113 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474185 | |||||
| chr6:17474186
|
T | G | 4 | a0001c0008t0001g0051a0001c0009t0001g0012a0001c0009t0001g0014others(1): Show | 4 | HG01361.hp2 HG02486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+11113T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474186 | ||||||
| chr6:17474187
|
T | C | 1 | a0001c0009t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.300+11114T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474187 | ||||||
| chr6:17474187
|
T | G | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+11114T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474187 | ||||||
| chr6:17474188
|
T | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+11115T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474188 | ||||||
| chr6:17474193
|
T | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+11120T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474193 | ||||||
| chr6:17474322
|
GA | G | 12 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(9): Show | 12 | HG01496.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+11259delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474322 | |||||
| chr6:17474569
|
C | T | 5 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+11496C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474569 | ||||||
| chr6:17474724
|
A | AT | 12 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0065others(9): Show | 12 | HG01496.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+11658dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474724 | |||||
| chr6:17474808
|
G | A | 2 | a0001c0001t0001g0085a0002c0004t0001g0089 | 2 | HG00735.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.300+11735G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474808 | ||||||
| chr6:17474970
|
G | A | 1 | a0002c0005t0001g0003 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.300+11897G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474970 | ||||||
| chr6:17475054
|
A | G | 2 | a0001c0002t0001g0107a0001c0002t0001g0184 | 2 | HG00099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.300+11981A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475054 | ||||||
| chr6:17475150
|
G | A | 5 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0002g0199others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+12077G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475150 | ||||||
| chr6:17475153
|
C | T | 5 | a0001c0001t0001g0085a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG00735.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+12080C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475153 | ||||||
| chr6:17475194
|
C | CA | 20 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0103others(17): Show | 20 | HG01109.hp2 HG01255.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.300+12136dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17475194 | |||||
| chr6:17475194
|
CA | C | 13 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0002t0001g0112others(10): Show | 13 | HG01496.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.300+12136delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17475194 | |||||
| chr6:17475206
|
A | AG | 10 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+12133_300+1213 others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475206 | ||||||
| chr6:17475227
|
C | A | 1 | a0001c0002t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.300+12154C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475227 | ||||||
| chr6:17475557
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.300+12484C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475557 | ||||||
| chr6:17475851
|
C | G | 1 | a0001c0001t0002g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.300+12778C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475851 | ||||||
| chr6:17475851
|
C | T | 1 | a0001c0001t0002g0172 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.300+12778C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475851 | ||||||
| chr6:17476230
|
T | C | 38 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0075others(35): Show | 38 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.300+13157T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476230 | ||||||
| chr6:17476360
|
T | C | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051 | 3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+13287T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476360 | ||||||
| chr6:17476382
|
G | A | 18 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0075others(15): Show | 18 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+13309G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476382 | ||||||
| chr6:17476525
|
C | T | 11 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0002g0050others(8): Show | 11 | HG00735.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+13452C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476525 | ||||||
| chr6:17476528
|
C | G | 2 | a0001c0009t0001g0014a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+13455C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476528 | ||||||
| chr6:17476794
|
T | G | 1 | a0001c0001t0002g0150 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.300+13721T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476794 | ||||||
| chr6:17476864
|
C | CT | 5 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0095others(2): Show | 5 | HG00438.hp1 HG01175.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+13816dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17476864 | |||||
| chr6:17476864
|
CT | C | 51 | a0001c0001t0001g0041a0001c0001t0001g0067a0001c0001t0001g0068others(48): Show | 51 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.300+13816delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17476864 | |||||
| chr6:17476864
|
CTT | C | 74 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(71): Show | 74 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(71): Show |
intron_variant | MODIFIER | c.300+13815_300+1381 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17476864 | |||||
| chr6:17476864
|
CTTT | C | 5 | a0001c0001t0001g0123a0001c0002t0001g0098a0001c0002t0001g0146others(2): Show | 5 | HG00609.hp1 HG00609.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+13814_300+1381 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17476864 | |||||
| chr6:17476864
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0039 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.300+13807_300+1381 others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17476864 | |||||
| chr6:17476909
|
C | T | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.300+13836C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476909 | ||||||
| chr6:17476936
|
A | G | 1 | a0002c0005t0004g0024 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.300+13863A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476936 | ||||||
| chr6:17477194
|
C | G | 76 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(73): Show | 76 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.300+14121C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477194 | ||||||
| chr6:17477266
|
G | C | 2 | a0001c0001t0002g0045a0001c0001t0002g0152 | 2 | HG01516.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.300+14193G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477266 | ||||||
| chr6:17477307
|
C | T | 2 | a0001c0002t0001g0132a0001c0003t0002g0131 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.300+14234C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477307 | ||||||
| chr6:17477346
|
G | A | 1 | a0001c0002t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.300+14273G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477346 | ||||||
| chr6:17477453
|
A | T | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.300+14380A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477453 | ||||||
| chr6:17477541
|
C | T | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.300+14468C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477541 | ||||||
| chr6:17477956
|
C | T | 117 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0053others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.300+14883C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477956 | ||||||
| chr6:17478003
|
A | G | 1 | a0002c0012t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.300+14930A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478003 | ||||||
| chr6:17478195
|
C | T | 5 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+15122C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478195 | ||||||
| chr6:17478242
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.300+15169C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478242 | ||||||
| chr6:17478297
|
C | CT | 36 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(33): Show | 36 | HG01109.hp2 HG01167.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.300+15244dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17478297 | |||||
| chr6:17478297
|
C | CTT | 5 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+15243_300+1524 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17478297 | |||||
| chr6:17478297
|
CT | C | 9 | a0001c0001t0001g0154a0001c0001t0002g0026a0001c0002t0001g0107others(6): Show | 9 | HG00099.hp2 HG01261.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+15244delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17478297 | |||||
| chr6:17478312
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.300+15239T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478312 | ||||||
| chr6:17478540
|
C | G | 10 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+15467C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478540 | ||||||
| chr6:17478832
|
A | C | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.300+15759A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478832 | ||||||
| chr6:17478868
|
T | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+15795T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478868 | ||||||
| chr6:17478999
|
C | T | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+15926C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478999 | ||||||
| chr6:17479070
|
G | A | 1 | a0001c0002t0001g0193 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.300+15997G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479070 | ||||||
| chr6:17479357
|
G | C | 113 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0052others(110): Show | 113 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.300+16284G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479357 | ||||||
| chr6:17479433
|
C | T | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+16360C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479433 | ||||||
| chr6:17479435
|
T | A | 11 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0084others(8): Show | 11 | HG02109.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+16362T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479435 | ||||||
| chr6:17479526
|
G | C | 18 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0075others(15): Show | 18 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+16453G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479526 | ||||||
| chr6:17479594
|
G | C | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+16521G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479594 | ||||||
| chr6:17479607
|
A | AT | 11 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0085others(8): Show | 11 | HG00735.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+16556dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17479607 | |||||
| chr6:17479607
|
AT | A | 41 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0068others(38): Show | 41 | HG00099.hp1 HG00642.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.300+16556delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17479607 | |||||
| chr6:17479607
|
ATTT | A | 9 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(6): Show | 9 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+16554_300+1655 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17479607 | |||||
| chr6:17479635
|
A | G | 5 | a0001c0001t0001g0085a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG00735.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+16562A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479635 | ||||||
| chr6:17479697
|
C | T | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+16624C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479697 | ||||||
| chr6:17479758
|
C | T | 1 | a0001c0001t0002g0181 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.300+16685C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479758 | ||||||
| chr6:17479761
|
G | A | 1 | a0001c0003t0002g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.300+16688G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479761 | ||||||
| chr6:17479802
|
A | G | 1 | a0001c0001t0002g0158 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.300+16729A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479802 | ||||||
| chr6:17479858
|
G | A | 115 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.300+16785G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479858 | ||||||
| chr6:17479866
|
C | T | 2 | a0001c0002t0001g0062a0001c0002t0002g0073 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.300+16793C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479866 | ||||||
| chr6:17479867
|
G | A | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+16794G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479867 | ||||||
| chr6:17480144
|
C | G | 1 | a0002c0004t0001g0089 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.300+17071C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480144 | ||||||
| chr6:17480156
|
G | A | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.300+17083G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480156 | ||||||
| chr6:17480294
|
G | T | 3 | a0001c0002t0001g0101a0001c0002t0001g0112a0001c0008t0001g0204 | 3 | HG02055.hp2 HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.300+17221G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480294 | ||||||
| chr6:17480639
|
T | A | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.300+17566T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480639 | ||||||
| chr6:17480761
|
G | A | 1 | a0002c0004t0001g0089 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.300+17688G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480761 | ||||||
| chr6:17480771
|
T | G | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.300+17698T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480771 | ||||||
| chr6:17480771
|
T | TG | 11 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0099others(8): Show | 11 | HG02027.hp1 HG02109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+17700dupG | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17480771 | |||||
| chr6:17480773
|
GT | G | 28 | a0001c0001t0001g0085a0001c0001t0002g0037a0001c0001t0002g0050others(25): Show | 28 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.300+17719delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17480773 | |||||
| chr6:17480774
|
T | G | 132 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(129): Show | 132 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.300+17701T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480774 | ||||||
| chr6:17480775
|
T | G | 28 | a0001c0001t0001g0085a0001c0001t0002g0037a0001c0001t0002g0050others(25): Show | 28 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.300+17702T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480775 | ||||||
| chr6:17480806
|
C | T | 3 | a0001c0002t0001g0058a0001c0002t0001g0090a0001c0008t0001g0057 | 3 | HG00642.hp1 HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.300+17733C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480806 | ||||||
| chr6:17480848
|
C | T | 8 | a0001c0001t0001g0069a0001c0001t0001g0196a0001c0001t0001g0202others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+17775C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480848 | ||||||
| chr6:17480860
|
C | A | 1 | a0001c0002t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.300+17787C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480860 | ||||||
| chr6:17480884
|
C | A | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.300+17811C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480884 | ||||||
| chr6:17480908
|
A | T | 1 | a0001c0002t0002g0114 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.300+17835A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480908 | ||||||
| chr6:17480921
|
G | C | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.300+17848G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480921 | ||||||
| chr6:17480923
|
T | G | 7 | a0001c0001t0002g0037a0001c0002t0001g0002a0001c0002t0001g0058others(4): Show | 7 | HG00642.hp1 HG01243.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+17850T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480923 | ||||||
| chr6:17480952
|
A | AT | 7 | a0001c0001t0001g0039a0001c0001t0001g0099a0001c0001t0001g0202others(4): Show | 7 | HG01106.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+17905dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17480952 | |||||
| chr6:17480952
|
A | ATT | 7 | a0001c0001t0001g0068a0001c0003t0001g0088a0001c0003t0001g0091others(4): Show | 7 | HG02109.hp1 HG02622.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+17904_300+1790 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17480952 | |||||
| chr6:17480952
|
AT | A | 121 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(118): Show | 121 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.300+17905delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17480952 | |||||
| chr6:17480952
|
ATT | A | 9 | a0001c0002t0001g0072a0001c0003t0001g0065a0001c0003t0002g0080others(6): Show | 9 | HG01361.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+17904_300+1790 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17480952 | |||||
| chr6:17481031
|
T | A | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+17958T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481031 | ||||||
| chr6:17481141
|
A | G | 32 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0142others(29): Show | 32 | HG00438.hp2 HG00597.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.300+18068A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481141 | ||||||
| chr6:17481273
|
C | A | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+18200C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481273 | ||||||
| chr6:17481452
|
A | AT | 171 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(168): Show | 171 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.300+18379_300+1838 others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481452 | ||||||
| chr6:17481453
|
C | A | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+18380C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481453 | ||||||
| chr6:17481644
|
T | C | 3 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0002g0131 | 3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.300+18571T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481644 | ||||||
| chr6:17481672
|
A | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.300+18599A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481672 | ||||||
| chr6:17481741
|
C | T | 3 | a0001c0003t0001g0065a0001c0009t0001g0014a0001c0014t0008g0015 | 3 | HG01361.hp2 HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+18668C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481741 | ||||||
| chr6:17481816
|
C | T | 53 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(50): Show | 53 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.300+18743C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481816 | ||||||
| chr6:17481851
|
G | C | 6 | a0001c0003t0001g0065a0001c0009t0001g0014a0001c0014t0008g0015others(3): Show | 6 | HG01361.hp2 HG01496.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.300+18778G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481851 | ||||||
| chr6:17482086
|
G | A | 54 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(51): Show | 54 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.300+19013G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482086 | ||||||
| chr6:17482146
|
C | T | 6 | a0001c0001t0002g0037a0001c0002t0001g0002a0001c0002t0001g0058others(3): Show | 6 | HG00642.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+19073C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482146 | ||||||
| chr6:17482221
|
C | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+19148C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482221 | ||||||
| chr6:17482449
|
C | G | 8 | a0001c0001t0001g0069a0001c0001t0001g0196a0001c0001t0001g0202others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+19376C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482449 | ||||||
| chr6:17482453
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.300+19380A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482453 | ||||||
| chr6:17482507
|
C | CA | 14 | a0001c0001t0001g0039a0001c0001t0001g0086a0001c0001t0002g0141others(11): Show | 14 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.300+19466dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | |||||
| chr6:17482507
|
C | CAA | 5 | a0001c0002t0001g0136a0001c0002t0001g0184a0001c0014t0008g0015others(2): Show | 5 | HG01175.hp1 HG01261.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+19465_300+1946 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | |||||
| chr6:17482507
|
CAA | C | 8 | a0001c0001t0001g0067a0001c0001t0002g0037a0001c0002t0001g0002others(5): Show | 8 | HG00642.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.300+19465_300+1946 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | |||||
| chr6:17482507
|
CAAA | C | 9 | a0001c0001t0001g0068a0001c0003t0001g0084a0001c0003t0001g0088others(6): Show | 9 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+19464_300+1946 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | |||||
| chr6:17482507
|
CAAAAAAA others(3): Show |
C | 15 | a0001c0001t0001g0018a0001c0001t0001g0074a0001c0001t0001g0075others(12): Show | 15 | HG00438.hp1 HG01167.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.300+19457_300+1946 others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | |||||
| chr6:17482507
|
CAAAAAAA others(4): Show |
C | 112 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(109): Show | 112 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.300+19456_300+1946 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | |||||
| chr6:17482507
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.300+19455_300+1946 others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | |||||
| chr6:17482507
|
CAAAAAAA others(8): Show |
C | 14 | a0001c0001t0001g0069a0001c0001t0001g0085a0001c0001t0001g0196others(11): Show | 14 | HG00735.hp2 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.300+19452_300+1946 others(19): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | |||||
| chr6:17482507
|
CAAAAAAA others(9): Show |
C | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+19451_300+1946 others(20): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | |||||
| chr6:17482540
|
G | A | 6 | a0001c0003t0001g0065a0001c0009t0001g0014a0001c0014t0008g0015others(3): Show | 6 | HG01361.hp2 HG01496.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.300+19467G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482540 | ||||||
| chr6:17482595
|
C | T | 3 | a0001c0003t0001g0065a0001c0009t0001g0014a0001c0014t0008g0015 | 3 | HG01361.hp2 HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+19522C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482595 | ||||||
| chr6:17482868
|
T | C | 1 | a0002c0004t0001g0089 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.300+19795T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482868 | ||||||
| chr6:17482889
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.300+19816C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482889 | ||||||
| chr6:17482974
|
C | T | 5 | a0001c0001t0001g0085a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG00735.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+19901C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482974 | ||||||
| chr6:17483151
|
TG | T | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+20082delG | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17483151 | |||||
| chr6:17483210
|
GTGTCT | G | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.300+20141_300+2014 others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17483210 | |||||
| chr6:17483298
|
G | T | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+20225G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483298 | ||||||
| chr6:17483329
|
T | C | 5 | a0001c0001t0001g0085a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG00735.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+20256T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483329 | ||||||
| chr6:17483339
|
T | C | 2 | a0001c0002t0001g0191a0001c0002t0001g0192 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.300+20266T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483339 | ||||||
| chr6:17483420
|
G | A | 1 | a0001c0002t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.300+20347G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483420 | ||||||
| chr6:17483437
|
A | G | 6 | a0001c0002t0001g0019a0001c0002t0001g0144a0001c0002t0001g0145others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.300+20364A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483437 | ||||||
| chr6:17483605
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.300+20532G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483605 | ||||||
| chr6:17483636
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.300+20563C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483636 | ||||||
| chr6:17483644
|
C | T | 127 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(124): Show | 127 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.300+20571C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483644 | ||||||
| chr6:17483808
|
T | G | 4 | a0001c0002t0001g0019a0001c0002t0001g0144a0001c0002t0001g0145others(1): Show | 4 | HG02486.hp1 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+20735T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483808 | ||||||
| chr6:17483850
|
A | G | 8 | a0001c0001t0001g0069a0001c0001t0001g0196a0001c0001t0001g0202others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+20777A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483850 | ||||||
| chr6:17483906
|
C | G | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051 | 3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+20833C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483906 | ||||||
| chr6:17483920
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.300+20847C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483920 | ||||||
| chr6:17483961
|
C | T | 4 | a0001c0001t0001g0085a0001c0002t0001g0130a0001c0002t0001g0132others(1): Show | 4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+20888C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483961 | ||||||
| chr6:17484021
|
C | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0009 | 2 | HG03831.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.300+20948C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484021 | ||||||
| chr6:17484112
|
G | C | 1 | a0001c0001t0002g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.300+21039G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484112 | ||||||
| chr6:17484122
|
T | G | 7 | a0001c0001t0001g0069a0001c0001t0001g0196a0001c0001t0002g0199others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.300+21049T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484122 | ||||||
| chr6:17484280
|
G | A | 14 | a0001c0001t0001g0069a0001c0001t0001g0196a0001c0001t0001g0202others(11): Show | 14 | HG00642.hp1 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.300+21207G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484280 | ||||||
| chr6:17484288
|
G | A | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+21215G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484288 | ||||||
| chr6:17484322
|
C | T | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.300+21249C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484322 | ||||||
| chr6:17484324
|
C | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.300+21251C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484324 | ||||||
| chr6:17484326
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.300+21253C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484326 | ||||||
| chr6:17484362
|
G | C | 1 | a0001c0002t0002g0114 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.300+21289G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484362 | ||||||
| chr6:17484372
|
G | A | 5 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+21299G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484372 | ||||||
| chr6:17484387
|
T | C | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+21314T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484387 | ||||||
| chr6:17484438
|
C | T | 4 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0002g0131others(1): Show | 4 | HG01255.hp1 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+21365C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484438 | ||||||
| chr6:17484484
|
A | C | 1 | a0001c0002t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.300+21411A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484484 | ||||||
| chr6:17484628
|
C | T | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.300+21555C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484628 | ||||||
| chr6:17484637
|
A | G | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.300+21564A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484637 | ||||||
| chr6:17484904
|
T | G | 1 | a0001c0001t0001g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.300+21831T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484904 | ||||||
| chr6:17484952
|
A | T | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.300+21879A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484952 | ||||||
| chr6:17485014
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.300+21941A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485014 | ||||||
| chr6:17485148
|
G | GT | 5 | a0001c0001t0002g0050a0001c0002t0001g0019a0001c0002t0001g0144others(2): Show | 5 | HG02486.hp1 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-22011dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17485148 | |||||
| chr6:17485148
|
G | T | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-22021G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485148 | ||||||
| chr6:17485309
|
A | C | 8 | a0001c0003t0001g0065a0001c0009t0001g0012a0001c0009t0001g0014others(5): Show | 8 | HG01361.hp2 HG01496.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-21860A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485309 | ||||||
| chr6:17485439
|
A | G | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-21730A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485439 | ||||||
| chr6:17485449
|
C | T | 4 | a0001c0001t0001g0085a0001c0002t0001g0130a0001c0002t0001g0132others(1): Show | 4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-21720C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485449 | ||||||
| chr6:17485616
|
A | T | 1 | a0001c0001t0001g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.301-21553A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485616 | ||||||
| chr6:17485673
|
A | T | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-21496A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485673 | ||||||
| chr6:17485828
|
T | C | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-21341T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485828 | ||||||
| chr6:17485856
|
C | T | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-21313C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485856 | ||||||
| chr6:17485890
|
G | A | 8 | a0001c0001t0001g0069a0001c0001t0001g0196a0001c0001t0002g0037others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.301-21279G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485890 | ||||||
| chr6:17485915
|
G | A | 6 | a0001c0003t0001g0065a0001c0009t0001g0014a0001c0014t0008g0015others(3): Show | 6 | HG01361.hp2 HG01496.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-21254G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485915 | ||||||
| chr6:17486281
|
C | T | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-20888C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486281 | ||||||
| chr6:17486437
|
C | T | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-20732C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486437 | ||||||
| chr6:17486457
|
T | C | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.301-20712T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486457 | ||||||
| chr6:17486536
|
G | A | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.301-20633G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486536 | ||||||
| chr6:17486765
|
G | A | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-20404G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486765 | ||||||
| chr6:17486893
|
AC | A | 41 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0075others(38): Show | 41 | HG00642.hp1 HG01109.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.301-20271delC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17486893 | |||||
| chr6:17486912
|
A | C | 5 | a0001c0001t0001g0044a0001c0001t0002g0010a0001c0001t0002g0042others(2): Show | 5 | HG00099.hp1 HG01175.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-20257A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486912 | ||||||
| chr6:17486921
|
A | G | 2 | a0001c0009t0001g0012a0001c0013t0001g0092 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-20248A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486921 | ||||||
| chr6:17487275
|
A | G | 56 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(53): Show | 56 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.301-19894A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487275 | ||||||
| chr6:17487340
|
T | C | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051 | 3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-19829T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487340 | ||||||
| chr6:17487406
|
T | C | 1 | a0001c0001t0002g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.301-19763T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487406 | ||||||
| chr6:17487452
|
GGTTT | G | 39 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0075others(36): Show | 39 | HG00642.hp1 HG01109.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.301-19688_301-1968 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17487452 | |||||
| chr6:17487538
|
T | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0178a0001c0001t0002g0172others(2): Show | 5 | HG02135.hp1 NA18612.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-19631T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487538 | ||||||
| chr6:17487562
|
C | T | 2 | a0001c0002t0001g0062a0001c0002t0002g0073 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.301-19607C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487562 | ||||||
| chr6:17487630
|
C | T | 10 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.301-19539C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487630 | ||||||
| chr6:17487678
|
C | T | 2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-19491C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487678 | ||||||
| chr6:17488004
|
G | A | 1 | a0001c0001t0005g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.301-19165G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488004 | ||||||
| chr6:17488033
|
T | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(38): Show | 41 | HG00438.hp1 HG01192.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.301-19136T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488033 | ||||||
| chr6:17488037
|
G | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(38): Show | 41 | HG00438.hp1 HG01192.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.301-19132G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488037 | ||||||
| chr6:17488068
|
C | G | 3 | a0001c0002t0001g0198a0001c0009t0001g0012a0001c0013t0001g0092 | 3 | HG02055.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.301-19101C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488068 | ||||||
| chr6:17488181
|
T | G | 8 | a0001c0001t0001g0085a0001c0002t0001g0130a0001c0002t0001g0132others(5): Show | 8 | HG01255.hp1 HG01361.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.301-18988T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488181 | ||||||
| chr6:17488287
|
T | G | 3 | a0001c0002t0001g0198a0001c0009t0001g0012a0001c0013t0001g0092 | 3 | HG02055.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.301-18882T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488287 | ||||||
| chr6:17488355
|
T | C | 3 | a0001c0002t0001g0198a0001c0009t0001g0012a0001c0013t0001g0092 | 3 | HG02055.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.301-18814T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488355 | ||||||
| chr6:17489001
|
C | T | 1 | a0001c0002t0001g0161 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.301-18168C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489001 | ||||||
| chr6:17489002
|
G | A | 2 | a0001c0001t0001g0099a0001c0002t0001g0100 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.301-18167G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489002 | ||||||
| chr6:17489123
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.301-18046C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489123 | ||||||
| chr6:17489204
|
C | T | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-17965C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489204 | ||||||
| chr6:17489301
|
A | T | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.301-17868A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489301 | ||||||
| chr6:17489331
|
C | T | 14 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0075others(11): Show | 14 | HG00735.hp2 HG01167.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.301-17838C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489331 | ||||||
| chr6:17489497
|
A | C | 3 | a0001c0002t0001g0130a0001c0002t0001g0132a0001c0003t0002g0131 | 3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.301-17672A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489497 | ||||||
| chr6:17489531
|
G | C | 1 | a0002c0012t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.301-17638G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489531 | ||||||
| chr6:17489589
|
C | T | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.301-17580C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489589 | ||||||
| chr6:17489593
|
T | G | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-17576T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489593 | ||||||
| chr6:17489656
|
G | C | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-17513G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489656 | ||||||
| chr6:17489687
|
G | A | 2 | a0002c0004t0002g0182a0002c0005t0001g0203 | 2 | NA19003.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.301-17482G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489687 | ||||||
| chr6:17489748
|
G | GA | 2 | a0001c0001t0001g0196a0001c0001t0005g0200 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.301-17420dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17489748 | |||||
| chr6:17490247
|
A | G | 1 | a0001c0003t0001g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.301-16922A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17490247 | ||||||
| chr6:17490284
|
A | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(5): Show | 8 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-16885A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17490284 | ||||||
| chr6:17490614
|
G | A | 6 | a0001c0002t0001g0107a0001c0002t0001g0128a0001c0002t0001g0136others(3): Show | 6 | HG00099.hp2 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-16555G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17490614 | ||||||
| chr6:17490653
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.301-16516G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17490653 | ||||||
| chr6:17491129
|
C | T | 9 | a0001c0001t0002g0102a0001c0002t0001g0108a0001c0002t0002g0111others(6): Show | 9 | HG01496.hp1 HG01928.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-16040C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491129 | ||||||
| chr6:17491172
|
A | G | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.301-15997A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491172 | ||||||
| chr6:17491174
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.301-15995G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491174 | ||||||
| chr6:17491485
|
T | C | 2 | a0001c0002t0001g0128a0001c0002t0001g0183 | 2 | HG01071.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.301-15684T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491485 | ||||||
| chr6:17491511
|
C | T | 17 | a0001c0001t0001g0052a0001c0002t0001g0019a0001c0002t0001g0130others(14): Show | 17 | HG00597.hp1 HG01361.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.301-15658C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491511 | ||||||
| chr6:17491721
|
G | A | 1 | a0001c0014t0008g0015 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.301-15448G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491721 | ||||||
| chr6:17491914
|
A | G | 2 | a0001c0002t0001g0093a0001c0002t0001g0094 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.301-15255A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491914 | ||||||
| chr6:17491928
|
T | A | 10 | a0001c0001t0001g0068a0001c0001t0002g0037a0001c0002t0001g0130others(7): Show | 10 | HG01255.hp1 HG01361.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.301-15241T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491928 | ||||||
| chr6:17491952
|
A | G | 1 | a0001c0002t0001g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.301-15217A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491952 | ||||||
| chr6:17492022
|
T | C | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.301-15147T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492022 | ||||||
| chr6:17492123
|
C | A | 4 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0009t0001g0012others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-15046C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492123 | ||||||
| chr6:17492159
|
G | A | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0008t0001g0051 | 3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-15010G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492159 | ||||||
| chr6:17492294
|
C | CAA | 6 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-14868_301-1486 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17492294 | |||||
| chr6:17492529
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.301-14640T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492529 | ||||||
| chr6:17492622
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.301-14547G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492622 | ||||||
| chr6:17492692
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.301-14477G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492692 | ||||||
| chr6:17492862
|
A | G | 120 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 120 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.301-14307A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492862 | ||||||
| chr6:17493077
|
A | T | 46 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0048others(43): Show | 46 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.301-14092A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17493077 | ||||||
| chr6:17493294
|
C | CT | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-13873dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17493294 | |||||
| chr6:17493330
|
A | AAGATATG others(9): Show |
3 | a0001c0001t0001g0028a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG01168.hp2 HG01975.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.301-13837_301-1382 others(20): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17493330 | |||||
| chr6:17493459
|
C | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(121): Show | 124 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.301-13710C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17493459 | ||||||
| chr6:17493564
|
C | G | 1 | a0001c0001t0001g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.301-13605C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17493564 | ||||||
| chr6:17493775
|
C | CA | 15 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(12): Show | 15 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.301-13379dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17493775 | |||||
| chr6:17493775
|
C | CAA | 44 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(41): Show | 44 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.301-13380_301-1337 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17493775 | |||||
| chr6:17493860
|
G | A | 1 | a0001c0002t0001g0019 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.301-13309G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17493860 | ||||||
| chr6:17493865
|
C | T | 1 | a0001c0014t0008g0015 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.301-13304C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17493865 | ||||||
| chr6:17493872
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0041others(91): Show | 94 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.301-13297G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17493872 | ||||||
| chr6:17494117
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0041others(92): Show | 95 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.301-13052A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494117 | ||||||
| chr6:17494139
|
G | A | 2 | a0001c0002t0001g0093a0001c0002t0001g0094 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.301-13030G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494139 | ||||||
| chr6:17494232
|
T | C | 44 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(41): Show | 44 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.301-12937T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494232 | ||||||
| chr6:17494334
|
G | A | 77 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0048others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.301-12835G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494334 | ||||||
| chr6:17494507
|
C | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0041others(91): Show | 94 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.301-12662C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494507 | ||||||
| chr6:17494547
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0041others(93): Show | 96 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.301-12622G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494547 | ||||||
| chr6:17494669
|
G | A | 7 | a0001c0003t0001g0038a0001c0003t0001g0084a0001c0003t0002g0060others(4): Show | 7 | HG02109.hp1 HG02647.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.301-12500G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494669 | ||||||
| chr6:17494776
|
C | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0041 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301-12393C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494776 | ||||||
| chr6:17494807
|
T | C | 1 | a0001c0002t0001g0098 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.301-12362T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494807 | ||||||
| chr6:17494903
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0041others(91): Show | 94 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.301-12266C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494903 | ||||||
| chr6:17494934
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.301-12235T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494934 | ||||||
| chr6:17494967
|
A | T | 1 | a0001c0002t0001g0136 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.301-12202A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494967 | ||||||
| chr6:17495108
|
C | G | 1 | a0001c0006t0001g0120 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.301-12061C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495108 | ||||||
| chr6:17495229
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.301-11940G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495229 | ||||||
| chr6:17495259
|
C | G | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-11910C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495259 | ||||||
| chr6:17495371
|
C | A | 123 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(120): Show | 123 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.301-11798C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495371 | ||||||
| chr6:17495448
|
C | G | 1 | a0001c0001t0002g0010 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.301-11721C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495448 | ||||||
| chr6:17495882
|
G | A | 6 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0196others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-11287G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495882 | ||||||
| chr6:17495939
|
C | G | 78 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0048others(75): Show | 78 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.301-11230C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495939 | ||||||
| chr6:17495968
|
C | T | 24 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(21): Show | 24 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.301-11201C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495968 | ||||||
| chr6:17496027
|
T | TG | 16 | a0001c0001t0001g0103a0001c0001t0001g0202a0001c0001t0002g0037others(13): Show | 16 | HG01109.hp2 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.301-11130dupG | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496027 | |||||
| chr6:17496027
|
T | TGGCG | 17 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0022others(14): Show | 17 | HG01071.hp2 HG01168.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.301-11140_301-1113 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496027 | |||||
| chr6:17496027
|
T | TGGCGG | 40 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(37): Show | 40 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.301-11140_301-1113 others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496027 | |||||
| chr6:17496027
|
T | TGGCGGG | 39 | a0001c0001t0001g0008a0001c0001t0001g0041a0001c0001t0001g0140others(36): Show | 39 | HG00438.hp2 HG00597.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.301-11140_301-1113 others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496027 | |||||
| chr6:17496027
|
T | TGGCGGGG others(4): Show |
1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.301-11140_301-1113 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496027 | |||||
| chr6:17496030
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.301-11139G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496030 | ||||||
| chr6:17496032
|
G | T | 4 | a0001c0002t0001g0035a0001c0002t0001g0188a0001c0002t0001g0189others(1): Show | 4 | HG00741.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-11137G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496032 | ||||||
| chr6:17496033
|
G | A | 6 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0196others(3): Show | 6 | HG01517.hp1 HG01884.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-11136G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496033 | ||||||
| chr6:17496033
|
G | GGT | 23 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(20): Show | 23 | HG00735.hp2 HG01167.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.301-11135_301-1113 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496033 | |||||
| chr6:17496036
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.301-11133G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496036 | ||||||
| chr6:17496036
|
G | T | 1 | a0001c0002t0001g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.301-11133G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496036 | ||||||
| chr6:17496037
|
G | T | 3 | a0001c0002t0001g0002a0002c0004t0002g0097a0002c0005t0003g0170 | 3 | HG02258.hp1 NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.301-11132G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496037 | ||||||
| chr6:17496141
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.301-11028A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496141 | ||||||
| chr6:17496303
|
C | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(149): Show | 152 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.301-10866C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496303 | ||||||
| chr6:17496326
|
A | AGTATCTT | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0009t0001g0012 | 3 | HG02145.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-10840_301-1083 others(11): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496326 | |||||
| chr6:17496440
|
C | T | 2 | a0001c0002t0001g0019a0001c0002t0002g0118 | 2 | HG03834.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.301-10729C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496440 | ||||||
| chr6:17496721
|
G | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-10448G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496721 | ||||||
| chr6:17496830
|
T | C | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-10339T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496830 | ||||||
| chr6:17497231
|
A | G | 49 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(46): Show | 49 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.301-9938A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17497231 | ||||||
| chr6:17497260
|
T | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(149): Show | 152 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.301-9909T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17497260 | ||||||
| chr6:17497361
|
C | T | 1 | a0001c0003t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.301-9808C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17497361 | ||||||
| chr6:17497704
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(126): Show | 129 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.301-9465T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17497704 | ||||||
| chr6:17498123
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.301-9046G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17498123 | ||||||
| chr6:17498346
|
G | A | 2 | a0001c0003t0002g0064a0001c0003t0002g0087 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.301-8823G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17498346 | ||||||
| chr6:17498622
|
T | C | 84 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(81): Show | 84 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.301-8547T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17498622 | ||||||
| chr6:17498864
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.301-8305G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17498864 | ||||||
| chr6:17498891
|
G | A | 1 | a0001c0002t0001g0138 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.301-8278G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17498891 | ||||||
| chr6:17499398
|
C | CA | 81 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0028others(78): Show | 81 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.301-7749dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499398 | |||||
| chr6:17499398
|
C | CAA | 5 | a0001c0001t0001g0069a0001c0001t0002g0043a0001c0002t0002g0073others(2): Show | 5 | HG01175.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-7750_301-7749d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499398 | |||||
| chr6:17499398
|
C | CAAAAAAA others(1): Show |
5 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-7756_301-7749d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499398 | |||||
| chr6:17499398
|
CA | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0159a0001c0002t0001g0153others(2): Show | 5 | HG02970.hp1 HG03017.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-7749delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499398 | |||||
| chr6:17499398
|
CAA | C | 16 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(13): Show | 16 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.301-7750_301-7749d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499398 | |||||
| chr6:17499612
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.301-7557G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17499612 | ||||||
| chr6:17499624
|
G | A | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-7545G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17499624 | ||||||
| chr6:17499657
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0041 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301-7512T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17499657 | ||||||
| chr6:17499848
|
C | CATAA | 51 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0028others(48): Show | 51 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.301-7291_301-7288d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499848 | |||||
| chr6:17499848
|
C | CATAAATA others(1): Show |
75 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(72): Show | 75 | HG00438.hp1 HG00597.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.301-7295_301-7288d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499848 | |||||
| chr6:17499848
|
C | CATAAATA others(5): Show |
23 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0025others(20): Show | 23 | HG01361.hp1 HG01361.hp2 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.301-7299_301-7288d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499848 | |||||
| chr6:17499848
|
C | CATAAATA others(9): Show |
1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.301-7303_301-7288d others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499848 | |||||
| chr6:17500284
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.301-6885G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500284 | ||||||
| chr6:17500340
|
A | AAT | 9 | a0001c0001t0001g0123a0001c0001t0002g0121a0001c0001t0002g0171others(6): Show | 9 | HG01928.hp2 HG02027.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-6786_301-6785d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATAT | 12 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0165others(9): Show | 12 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-6788_301-6785d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATAT | 10 | a0001c0001t0001g0044a0001c0002t0001g0094a0001c0002t0001g0098others(7): Show | 10 | HG00099.hp1 HG00741.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.301-6790_301-6785d others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATATA others(1): Show |
18 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 18 | HG00609.hp1 HG01071.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.301-6792_301-6785d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATATA others(3): Show |
19 | a0001c0001t0001g0069a0001c0001t0001g0142a0001c0001t0002g0023others(16): Show | 19 | HG00099.hp2 HG01175.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.301-6794_301-6785d others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATATA others(5): Show |
28 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0075others(25): Show | 28 | HG01106.hp2 HG01109.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.301-6796_301-6785d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATATA others(7): Show |
14 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0095others(11): Show | 14 | HG00438.hp1 HG00735.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.301-6798_301-6785d others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATATA others(9): Show |
7 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0086others(4): Show | 7 | HG00741.hp2 HG01168.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-6800_301-6785d others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATATA others(11): Show |
14 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0103others(11): Show | 14 | HG00735.hp1 HG01109.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.301-6802_301-6785d others(20): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATATA others(13): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0174others(4): Show | 7 | HG02027.hp2 HG02071.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-6804_301-6785d others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATATA others(15): Show |
5 | a0001c0001t0001g0009a0001c0001t0001g0099a0001c0001t0002g0162others(2): Show | 5 | HG02818.hp2 HG03195.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-6806_301-6785d others(24): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATATA others(17): Show |
2 | a0001c0001t0002g0137a0001c0002t0001g0125 | 2 | HG01071.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.301-6808_301-6785d others(26): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATATA others(19): Show |
3 | a0001c0001t0001g0007a0001c0001t0002g0027a0004c0010t0001g0063 | 3 | HG01192.hp1 HG02897.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.301-6810_301-6785d others(28): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATATA others(21): Show |
1 | a0002c0005t0001g0003 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.301-6812_301-6785d others(30): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATATA others(25): Show |
1 | a0001c0002t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.301-6816_301-6785d others(34): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | AATATATA others(27): Show |
1 | a0001c0001t0002g0126 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.301-6818_301-6785d others(36): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0145 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.301-6829_301-6828i others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500340 | ||||||
| chr6:17500340
|
A | ATATATAT others(6): Show |
1 | a0002c0004t0002g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.301-6829_301-6828i others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500340 | ||||||
| chr6:17500340
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.301-6829_301-6828i others(23): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500340 | ||||||
| chr6:17500340
|
AAT | A | 11 | a0001c0001t0001g0054a0001c0001t0001g0180a0001c0001t0002g0096others(8): Show | 11 | HG00597.hp2 HG01928.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.301-6786_301-6785d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
AATAT | A | 4 | a0001c0001t0001g0053a0001c0001t0002g0026a0001c0002t0001g0056others(1): Show | 4 | HG03669.hp2 HG04228.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-6788_301-6785d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
AATATAT | A | 4 | a0001c0001t0001g0016a0001c0002t0001g0005a0001c0002t0001g0062others(1): Show | 4 | HG02109.hp2 HG03491.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-6790_301-6785d others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
AATATATA others(3): Show |
A | 1 | a0001c0003t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.301-6794_301-6785d others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
AATATATA others(5): Show |
A | 2 | a0001c0001t0001g0020a0001c0001t0002g0021 | 2 | HG02083.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.301-6796_301-6785d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
AATATATA others(9): Show |
A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.301-6800_301-6785d others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
AATATATA others(13): Show |
A | 5 | a0001c0001t0002g0102a0001c0001t0002g0147a0001c0001t0002g0169others(2): Show | 5 | HG01255.hp2 HG01261.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-6804_301-6785d others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
AATATATA others(19): Show |
A | 1 | a0001c0001t0002g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.301-6810_301-6785d others(28): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
AATATATA others(21): Show |
A | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.301-6812_301-6785d others(30): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500340
|
AATATATA others(25): Show |
A | 3 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0124 | 3 | HG02280.hp1 HG02738.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301-6816_301-6785d others(34): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | |||||
| chr6:17500368
|
T | TATATATA others(21): Show |
1 | a0001c0014t0008g0015 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.301-6785_301-6784i others(30): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500368 | |||||
| chr6:17500384
|
T | TATATATA others(4): Show |
1 | a0001c0001t0001g0151 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.301-6785_301-6784i others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500384 | ||||||
| chr6:17500384
|
T | TATATATA others(14): Show |
1 | a0001c0001t0002g0031 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.301-6785_301-6784i others(23): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500384 | ||||||
| chr6:17500431
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.301-6738C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500431 | ||||||
| chr6:17500762
|
A | G | 1 | a0001c0014t0008g0015 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.301-6407A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500762 | ||||||
| chr6:17500846
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.301-6323C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500846 | ||||||
| chr6:17500908
|
A | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.301-6261A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500908 | ||||||
| chr6:17501122
|
G | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0041 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301-6047G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501122 | ||||||
| chr6:17501327
|
G | A | 1 | a0001c0003t0002g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.301-5842G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501327 | ||||||
| chr6:17501382
|
C | G | 1 | a0001c0014t0008g0015 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.301-5787C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501382 | ||||||
| chr6:17501447
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.301-5722T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501447 | ||||||
| chr6:17501476
|
G | A | 12 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(9): Show | 12 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-5693G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501476 | ||||||
| chr6:17501836
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.301-5333G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501836 | ||||||
| chr6:17501880
|
C | T | 12 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(9): Show | 12 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-5289C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501880 | ||||||
| chr6:17502039
|
T | C | 1 | a0006c0016t0001g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.301-5130T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17502039 | ||||||
| chr6:17502083
|
G | A | 1 | a0002c0012t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.301-5086G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17502083 | ||||||
| chr6:17502705
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(150): Show | 153 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.301-4464T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17502705 | ||||||
| chr6:17502891
|
C | T | 12 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(9): Show | 12 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-4278C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17502891 | ||||||
| chr6:17503180
|
G | A | 2 | a0001c0002t0001g0125a0001c0002t0002g0129 | 2 | HG01167.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.301-3989G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503180 | ||||||
| chr6:17503275
|
C | T | 2 | a0001c0002t0001g0107a0001c0002t0001g0184 | 2 | HG00099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.301-3894C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503275 | ||||||
| chr6:17503320
|
C | G | 1 | a0001c0003t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.301-3849C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503320 | ||||||
| chr6:17503477
|
G | A | 1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.301-3692G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503477 | ||||||
| chr6:17503559
|
G | A | 12 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(9): Show | 12 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-3610G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503559 | ||||||
| chr6:17503563
|
C | T | 12 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(9): Show | 12 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-3606C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503563 | ||||||
| chr6:17503598
|
C | G | 84 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(81): Show | 84 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.301-3571C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503598 | ||||||
| chr6:17503604
|
C | CA | 15 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0022others(12): Show | 15 | HG01106.hp1 HG01106.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.301-3544dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17503604 | |||||
| chr6:17503604
|
CA | C | 25 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(22): Show | 25 | HG00597.hp1 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.301-3544delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17503604 | |||||
| chr6:17503698
|
A | G | 1 | a0001c0001t0002g0027 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.301-3471A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503698 | ||||||
| chr6:17503971
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.301-3198A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503971 | ||||||
| chr6:17504177
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.301-2992T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504177 | ||||||
| chr6:17504271
|
A | C | 142 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(139): Show | 142 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.301-2898A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504271 | ||||||
| chr6:17504337
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.301-2832T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504337 | ||||||
| chr6:17504344
|
T | A | 1 | a0001c0001t0002g0030 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.301-2825T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504344 | ||||||
| chr6:17504345
|
G | T | 1 | a0001c0001t0002g0030 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.301-2824G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504345 | ||||||
| chr6:17504346
|
G | T | 1 | a0001c0001t0002g0030 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.301-2823G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504346 | ||||||
| chr6:17504347
|
T | G | 1 | a0001c0001t0002g0030 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.301-2822T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504347 | ||||||
| chr6:17504537
|
G | A | 1 | a0001c0002t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.301-2632G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504537 | ||||||
| chr6:17504861
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.301-2308T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504861 | ||||||
| chr6:17505073
|
C | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0041 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301-2096C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505073 | ||||||
| chr6:17505114
|
C | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-2055C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505114 | ||||||
| chr6:17505158
|
T | G | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-2011T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505158 | ||||||
| chr6:17505326
|
C | T | 1 | a0001c0002t0002g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.301-1843C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505326 | ||||||
| chr6:17505518
|
T | A | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.301-1651T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505518 | ||||||
| chr6:17505532
|
C | T | 1 | a0002c0004t0002g0097 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.301-1637C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505532 | ||||||
| chr6:17505713
|
A | G | 134 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(131): Show | 134 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.301-1456A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505713 | ||||||
| chr6:17505841
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.301-1328C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505841 | ||||||
| chr6:17505880
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(150): Show | 153 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.301-1289C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505880 | ||||||
| chr6:17505885
|
C | T | 134 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(131): Show | 134 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.301-1284C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505885 | ||||||
| chr6:17506017
|
C | G | 1 | a0006c0016t0001g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.301-1152C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506017 | ||||||
| chr6:17506035
|
C | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-1134C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506035 | ||||||
| chr6:17506075
|
T | A | 1 | a0002c0004t0002g0182 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.301-1094T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506075 | ||||||
| chr6:17506360
|
T | C | 1 | a0002c0012t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.301-809T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506360 | ||||||
| chr6:17506404
|
G | A | 1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.301-765G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506404 | ||||||
| chr6:17506490
|
A | C | 2 | a0001c0003t0002g0047a0004c0010t0002g0061 | 2 | HG01255.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.301-679A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506490 | ||||||
| chr6:17506569
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG01167.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-600G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506569 | ||||||
| chr6:17506596
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0041 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301-573C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506596 | ||||||
| chr6:17506637
|
CA | C | 97 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(94): Show | 97 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.301-520delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17506637 | |||||
| chr6:17506717
|
A | G | 1 | a0001c0001t0002g0021 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.301-452A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506717 | ||||||
| chr6:17506793
|
A | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(148): Show | 151 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.301-376A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506793 | ||||||
| chr6:17506817
|
T | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.301-352T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506817 | ||||||
| chr6:17506946
|
T | C | 2 | a0001c0002t0001g0005a0001c0002t0001g0153 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.301-223T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506946 | ||||||
| chr6:17507025
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0022 | 2 | HG02027.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.301-144T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17507025 | ||||||
| chr6:17507035
|
G | C | 1 | a0001c0002t0001g0190 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.301-134G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17507035 | ||||||
| chr6:17507042
|
A | G | 2 | a0001c0002t0001g0101a0001c0002t0001g0112 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.301-127A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17507042 | ||||||
| chr6:17507439
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(152): Show | 155 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.444+127A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 5/12 | chr6 | 17507439 | ||||||
| chr6:17507485
|
C | A | 2 | a0001c0002t0001g0005a0001c0002t0001g0153 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.445-156C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 5/12 | chr6 | 17507485 | ||||||
| chr6:17507730
|
C | A | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | splice_region_variant&intron_variant | LOW | c.530+4C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17507730 | ||||||
| chr6:17507915
|
T | C | 2 | a0001c0002t0001g0130a0001c0002t0001g0132 | 2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.530+189T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17507915 | ||||||
| chr6:17507992
|
T | A | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.530+266T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17507992 | ||||||
| chr6:17508593
|
A | G | 145 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(142): Show | 145 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.530+867A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17508593 | ||||||
| chr6:17508755
|
C | CT | 105 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0028others(102): Show | 105 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.530+1042dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 17508755 | |||||
| chr6:17508755
|
C | CTT | 11 | a0001c0001t0001g0069a0001c0001t0001g0083a0001c0001t0001g0085others(8): Show | 11 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.530+1041_530+1042d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 17508755 | |||||
| chr6:17508755
|
C | CTTT | 26 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0016others(23): Show | 26 | HG00438.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.530+1040_530+1042d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 17508755 | |||||
| chr6:17508755
|
C | CTTTT | 6 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0074others(3): Show | 6 | HG01167.hp2 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.530+1039_530+1042d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 17508755 | |||||
| chr6:17508782
|
A | G | 36 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(33): Show | 36 | HG00438.hp1 HG00735.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.530+1056A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17508782 | ||||||
| chr6:17508838
|
A | C | 2 | a0001c0002t0001g0191a0001c0002t0001g0192 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.530+1112A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17508838 | ||||||
| chr6:17508997
|
C | T | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.530+1271C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17508997 | ||||||
| chr6:17509161
|
A | C | 1 | a0001c0002t0001g0164 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.530+1435A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17509161 | ||||||
| chr6:17509185
|
G | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.530+1459G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17509185 | ||||||
| chr6:17509388
|
A | G | 2 | a0001c0002t0001g0191a0001c0002t0001g0192 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.530+1662A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17509388 | ||||||
| chr6:17509532
|
G | A | 1 | a0002c0012t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.530+1806G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17509532 | ||||||
| chr6:17509541
|
G | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.530+1815G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17509541 | ||||||
| chr6:17509656
|
C | G | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.530+1930C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17509656 | ||||||
| chr6:17510028
|
A | T | 1 | a0001c0001t0001g0022 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.530+2302A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17510028 | ||||||
| chr6:17510065
|
G | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0124others(2): Show | 5 | HG02071.hp1 HG02071.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+2339G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17510065 | ||||||
| chr6:17510198
|
G | A | 13 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(10): Show | 13 | HG00597.hp1 HG01891.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.530+2472G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17510198 | ||||||
| chr6:17510270
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.530+2544A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17510270 | ||||||
| chr6:17510889
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.531-2960G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17510889 | ||||||
| chr6:17510895
|
C | T | 1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.531-2954C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17510895 | ||||||
| chr6:17511100
|
A | G | 7 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0086others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.531-2749A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511100 | ||||||
| chr6:17511216
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.531-2633G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511216 | ||||||
| chr6:17511256
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(40): Show | 43 | HG00438.hp1 HG00735.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.531-2593C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511256 | ||||||
| chr6:17511271
|
C | T | 9 | a0001c0001t0001g0069a0001c0001t0001g0083a0001c0001t0001g0085others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.531-2578C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511271 | ||||||
| chr6:17511364
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.531-2485T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511364 | ||||||
| chr6:17511396
|
T | C | 11 | a0001c0002t0001g0108a0001c0002t0001g0166a0001c0002t0002g0111others(8): Show | 11 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.531-2453T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511396 | ||||||
| chr6:17511450
|
C | T | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.531-2399C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511450 | ||||||
| chr6:17511474
|
C | G | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.531-2375C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511474 | ||||||
| chr6:17511517
|
T | C | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0002t0001g0198 | 3 | HG02630.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.531-2332T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511517 | ||||||
| chr6:17511537
|
T | C | 132 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 132 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.531-2312T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511537 | ||||||
| chr6:17511744
|
C | G | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.531-2105C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511744 | ||||||
| chr6:17511821
|
G | C | 5 | a0001c0001t0002g0050a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG01255.hp1 HG02486.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.531-2028G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511821 | ||||||
| chr6:17511823
|
C | A | 57 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(54): Show | 57 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.531-2026C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511823 | ||||||
| chr6:17511889
|
G | T | 24 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(21): Show | 24 | HG00438.hp1 HG00741.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.531-1960G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511889 | ||||||
| chr6:17512225
|
T | C | 1 | a0002c0004t0002g0077 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.531-1624T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512225 | ||||||
| chr6:17512401
|
A | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-1448A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512401 | ||||||
| chr6:17512411
|
G | A | 91 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(88): Show | 91 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.531-1438G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512411 | ||||||
| chr6:17512599
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(151): Show | 154 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.531-1250T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512599 | ||||||
| chr6:17512637
|
G | A | 2 | a0001c0002t0001g0098a0001c0002t0001g0161 | 2 | HG00609.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.531-1212G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512637 | ||||||
| chr6:17512748
|
A | T | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-1101A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512748 | ||||||
| chr6:17512751
|
C | G | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.531-1098C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512751 | ||||||
| chr6:17512752
|
A | T | 1 | a0002c0005t0003g0170 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.531-1097A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512752 | ||||||
| chr6:17513100
|
A | T | 1 | a0001c0011t0002g0081 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.531-749A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17513100 | ||||||
| chr6:17513424
|
C | CT | 8 | a0001c0003t0001g0065a0001c0003t0001g0082a0001c0003t0001g0088others(5): Show | 8 | HG01361.hp2 HG01496.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.531-416dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 17513424 | |||||
| chr6:17513723
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(151): Show | 154 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.531-126T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17513723 | ||||||
| chr6:17513747
|
C | A | 1 | a0001c0002t0002g0129 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.531-102C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17513747 | ||||||
| chr6:17514101
|
C | A | 9 | a0001c0001t0001g0069a0001c0001t0001g0083a0001c0001t0001g0085others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.636+147C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514101 | ||||||
| chr6:17514174
|
C | T | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.636+220C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514174 | ||||||
| chr6:17514231
|
C | T | 1 | a0001c0006t0001g0120 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.636+277C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514231 | ||||||
| chr6:17514232
|
G | A | 1 | a0001c0002t0002g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.636+278G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514232 | ||||||
| chr6:17514312
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.636+358G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514312 | ||||||
| chr6:17514364
|
A | G | 6 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.636+410A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514364 | ||||||
| chr6:17514406
|
G | T | 57 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(54): Show | 57 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.636+452G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514406 | ||||||
| chr6:17514502
|
C | A | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0002t0001g0198 | 3 | HG02630.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.636+548C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514502 | ||||||
| chr6:17514582
|
T | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(79): Show | 82 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.636+628T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514582 | ||||||
| chr6:17514834
|
G | T | 2 | a0001c0002t0001g0005a0001c0002t0001g0153 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.636+880G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514834 | ||||||
| chr6:17514863
|
T | A | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+909T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514863 | ||||||
| chr6:17514867
|
T | C | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+913T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514867 | ||||||
| chr6:17514869
|
G | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.636+915G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514869 | ||||||
| chr6:17514877
|
TTA | T | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+925_636+926del others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17514877 | |||||
| chr6:17514983
|
C | T | 10 | a0001c0001t0002g0150a0002c0004t0002g0097a0002c0004t0002g0156others(7): Show | 10 | HG00597.hp1 HG01884.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.636+1029C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514983 | ||||||
| chr6:17514995
|
C | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.636+1041C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514995 | ||||||
| chr6:17515190
|
C | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.636+1236C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17515190 | ||||||
| chr6:17515749
|
T | C | 10 | a0001c0001t0002g0150a0002c0004t0002g0097a0002c0004t0002g0156others(7): Show | 10 | HG00597.hp1 HG01884.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.636+1795T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17515749 | ||||||
| chr6:17515758
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.636+1804G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17515758 | ||||||
| chr6:17515931
|
C | A | 9 | a0001c0001t0001g0069a0001c0001t0001g0083a0001c0001t0001g0085others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.636+1977C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17515931 | ||||||
| chr6:17515991
|
G | A | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.636+2037G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17515991 | ||||||
| chr6:17516476
|
G | C | 1 | a0001c0001t0001g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.636+2522G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17516476 | ||||||
| chr6:17516940
|
T | G | 53 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(50): Show | 53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.636+2986T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17516940 | ||||||
| chr6:17517216
|
A | G | 10 | a0001c0001t0002g0150a0002c0004t0002g0097a0002c0004t0002g0156others(7): Show | 10 | HG00597.hp1 HG01884.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.636+3262A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517216 | ||||||
| chr6:17517425
|
T | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.636+3471T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517425 | ||||||
| chr6:17517459
|
G | T | 6 | a0001c0003t0001g0065a0001c0003t0001g0082a0001c0003t0001g0088others(3): Show | 6 | HG01361.hp2 HG01496.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.636+3505G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517459 | ||||||
| chr6:17517503
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0028others(67): Show | 70 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.636+3549C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517503 | ||||||
| chr6:17517508
|
A | C | 53 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(50): Show | 53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.636+3554A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517508 | ||||||
| chr6:17517605
|
T | A | 1 | a0001c0002t0001g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.636+3651T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517605 | ||||||
| chr6:17517672
|
A | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(147): Show | 150 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.636+3718A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517672 | ||||||
| chr6:17517680
|
C | A | 2 | a0001c0002t0001g0011a0001c0002t0001g0134 | 2 | HG03239.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.636+3726C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517680 | ||||||
| chr6:17517715
|
A | G | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.636+3761A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517715 | ||||||
| chr6:17517844
|
T | C | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.636+3890T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517844 | ||||||
| chr6:17517856
|
G | A | 54 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(51): Show | 54 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.636+3902G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517856 | ||||||
| chr6:17517902
|
A | AAAAT | 3 | a0001c0003t0002g0047a0001c0014t0008g0015a0005c0015t0001g0070 | 3 | HG01361.hp2 HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.636+3970_636+3973d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17517902 | |||||
| chr6:17517902
|
A | AAAATAAA others(1): Show |
5 | a0001c0003t0001g0065a0001c0003t0001g0082a0001c0003t0001g0088others(2): Show | 5 | HG01496.hp2 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+3966_636+3973d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17517902 | |||||
| chr6:17518033
|
C | T | 2 | a0001c0002t0001g0098a0001c0002t0001g0161 | 2 | HG00609.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.636+4079C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518033 | ||||||
| chr6:17518244
|
T | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(65): Show | 68 | HG00438.hp1 HG00735.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.636+4290T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518244 | ||||||
| chr6:17518389
|
T | C | 1 | a0001c0002t0001g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.636+4435T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518389 | ||||||
| chr6:17518542
|
T | G | 1 | a0001c0002t0001g0062 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.636+4588T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518542 | ||||||
| chr6:17518848
|
G | C | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.636+4894G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518848 | ||||||
| chr6:17518861
|
C | T | 53 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(50): Show | 53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.636+4907C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518861 | ||||||
| chr6:17518917
|
C | T | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.636+4963C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518917 | ||||||
| chr6:17519024
|
C | T | 13 | a0002c0004t0001g0089a0002c0004t0002g0077a0002c0004t0002g0079others(10): Show | 13 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.636+5070C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519024 | ||||||
| chr6:17519035
|
C | T | 1 | a0001c0002t0006g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.636+5081C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519035 | ||||||
| chr6:17519104
|
G | A | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.636+5150G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519104 | ||||||
| chr6:17519337
|
A | G | 2 | a0001c0002t0001g0002a0001c0002t0001g0062 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.636+5383A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519337 | ||||||
| chr6:17519400
|
G | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(28): Show | 31 | HG00438.hp1 HG00741.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.636+5446G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519400 | ||||||
| chr6:17519645
|
C | G | 1 | a0001c0002t0006g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.636+5691C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519645 | ||||||
| chr6:17519789
|
C | G | 1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.636+5835C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519789 | ||||||
| chr6:17519824
|
T | C | 56 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(53): Show | 56 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.636+5870T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519824 | ||||||
| chr6:17519877
|
G | A | 13 | a0001c0001t0002g0150a0002c0004t0001g0089a0002c0004t0002g0077others(10): Show | 13 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.636+5923G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519877 | ||||||
| chr6:17520118
|
GT | G | 6 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0002g0023others(3): Show | 6 | HG00642.hp2 HG00735.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.636+6171delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17520118 | |||||
| chr6:17520252
|
C | G | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.636+6298C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520252 | ||||||
| chr6:17520282
|
A | AT | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.636+6336dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17520282 | |||||
| chr6:17520298
|
C | T | 1 | a0001c0011t0002g0081 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.636+6344C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520298 | ||||||
| chr6:17520325
|
G | T | 59 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(56): Show | 59 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.636+6371G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520325 | ||||||
| chr6:17520353
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.636+6399G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520353 | ||||||
| chr6:17520575
|
A | G | 44 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(41): Show | 44 | HG00438.hp1 HG00741.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.636+6621A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520575 | ||||||
| chr6:17520840
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.636+6886A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520840 | ||||||
| chr6:17520942
|
C | G | 1 | a0001c0002t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.636+6988C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520942 | ||||||
| chr6:17521013
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.636+7059G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521013 | ||||||
| chr6:17521020
|
T | C | 1 | a0001c0002t0001g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.636+7066T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521020 | ||||||
| chr6:17521140
|
C | T | 53 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(50): Show | 53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.636+7186C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521140 | ||||||
| chr6:17521165
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.636+7211G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521165 | ||||||
| chr6:17521169
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.636+7215T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521169 | ||||||
| chr6:17521258
|
C | CA | 91 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(88): Show | 91 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.636+7315dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17521258 | |||||
| chr6:17521277
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.636+7323C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521277 | ||||||
| chr6:17521375
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(95): Show | 98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+7421A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521375 | ||||||
| chr6:17521508
|
G | T | 56 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(53): Show | 56 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.636+7554G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521508 | ||||||
| chr6:17521724
|
TG | T | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+7771delG | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521724 | ||||||
| chr6:17521726
|
C | T | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+7772C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521726 | ||||||
| chr6:17521752
|
C | T | 53 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(50): Show | 53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.636+7798C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521752 | ||||||
| chr6:17521887
|
T | C | 5 | a0001c0001t0002g0050a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG01255.hp1 HG02486.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.636+7933T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521887 | ||||||
| chr6:17521894
|
A | G | 2 | a0001c0002t0001g0108a0001c0002t0002g0116 | 2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.636+7940A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521894 | ||||||
| chr6:17521906
|
C | T | 12 | a0002c0004t0001g0089a0002c0004t0002g0077a0002c0004t0002g0079others(9): Show | 12 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.636+7952C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521906 | ||||||
| chr6:17521920
|
C | A | 1 | a0001c0001t0001g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.636+7966C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521920 | ||||||
| chr6:17521936
|
C | A | 3 | a0001c0002t0001g0107a0001c0002t0001g0136a0001c0002t0001g0184 | 3 | HG00099.hp2 HG01175.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.636+7982C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521936 | ||||||
| chr6:17522065
|
C | T | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+8111C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522065 | ||||||
| chr6:17522088
|
G | A | 8 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0086others(5): Show | 8 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.636+8134G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522088 | ||||||
| chr6:17522137
|
A | G | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+8183A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522137 | ||||||
| chr6:17522222
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.636+8268T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522222 | ||||||
| chr6:17522279
|
A | T | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.636+8325A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522279 | ||||||
| chr6:17522620
|
C | T | 12 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0002g0010others(9): Show | 12 | HG00642.hp2 HG00735.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.636+8666C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522620 | ||||||
| chr6:17522750
|
G | A | 6 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0002g0023others(3): Show | 6 | HG00642.hp2 HG00735.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.636+8796G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522750 | ||||||
| chr6:17522755
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(95): Show | 98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+8801T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522755 | ||||||
| chr6:17523016
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.636+9062G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523016 | ||||||
| chr6:17523076
|
A | T | 6 | a0001c0003t0001g0065a0001c0003t0001g0082a0001c0003t0001g0088others(3): Show | 6 | HG01361.hp2 HG01496.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.636+9122A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523076 | ||||||
| chr6:17523081
|
G | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(64): Show | 67 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.636+9127G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523081 | ||||||
| chr6:17523130
|
C | T | 3 | a0001c0002t0001g0090a0001c0002t0001g0101a0001c0002t0001g0112 | 3 | HG01243.hp1 HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.636+9176C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523130 | ||||||
| chr6:17523259
|
A | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(64): Show | 67 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.636+9305A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523259 | ||||||
| chr6:17523317
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(64): Show | 67 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.636+9363G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523317 | ||||||
| chr6:17523339
|
G | A | 4 | a0001c0003t0001g0065a0001c0003t0001g0082a0001c0003t0001g0088others(1): Show | 4 | HG01496.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+9385G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523339 | ||||||
| chr6:17523504
|
C | T | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+9550C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523504 | ||||||
| chr6:17523904
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.636+9950T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523904 | ||||||
| chr6:17523941
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.636+9987A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523941 | ||||||
| chr6:17524012
|
G | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(64): Show | 67 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.636+10058G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524012 | ||||||
| chr6:17524074
|
C | CA | 8 | a0001c0001t0001g0095a0001c0002t0001g0101a0001c0002t0001g0134others(5): Show | 8 | HG00438.hp1 HG01192.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.636+10142dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17524074 | |||||
| chr6:17524074
|
CA | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(46): Show | 49 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.636+10142delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17524074 | |||||
| chr6:17524074
|
CAA | C | 19 | a0001c0001t0001g0069a0001c0002t0001g0019a0001c0002t0001g0071others(16): Show | 19 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.636+10141_636+1014 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17524074 | |||||
| chr6:17524074
|
CAAAAAAA others(4): Show |
C | 53 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(50): Show | 53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.636+10132_636+1014 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17524074 | |||||
| chr6:17524076
|
A | G | 5 | a0001c0002t0002g0073a0001c0003t0002g0047a0003c0007t0001g0059others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+10122A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524076 | ||||||
| chr6:17524077
|
A | G | 18 | a0001c0002t0001g0019a0001c0002t0001g0071a0001c0002t0001g0072others(15): Show | 18 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.636+10123A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524077 | ||||||
| chr6:17524159
|
G | A | 13 | a0001c0001t0002g0150a0002c0004t0001g0089a0002c0004t0002g0077others(10): Show | 13 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.636+10205G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524159 | ||||||
| chr6:17524202
|
G | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.636+10248G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524202 | ||||||
| chr6:17524301
|
A | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(64): Show | 67 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.636+10347A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524301 | ||||||
| chr6:17524338
|
A | C | 2 | a0001c0001t0002g0126a0001c0001t0002g0175 | 2 | NA18747.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.636+10384A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524338 | ||||||
| chr6:17524346
|
T | C | 1 | a0001c0002t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.636+10392T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524346 | ||||||
| chr6:17524396
|
G | A | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+10442G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524396 | ||||||
| chr6:17524506
|
C | T | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.636+10552C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524506 | ||||||
| chr6:17524722
|
A | G | 1 | a0001c0001t0002g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.636+10768A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524722 | ||||||
| chr6:17524893
|
C | CTT | 5 | a0001c0003t0002g0047a0001c0009t0001g0014a0003c0007t0001g0059others(2): Show | 5 | HG02280.hp2 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.636+10955_636+1095 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17524893 | |||||
| chr6:17524893
|
CT | C | 175 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(172): Show | 175 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.636+10956delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17524893 | |||||
| chr6:17524899
|
T | C | 52 | a0001c0001t0001g0028a0001c0001t0001g0044a0001c0001t0001g0048others(49): Show | 52 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.636+10945T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524899 | ||||||
| chr6:17525021
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(28): Show | 31 | HG00438.hp1 HG00741.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.636+11067C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525021 | ||||||
| chr6:17525044
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.636+11090G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525044 | ||||||
| chr6:17525150
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.636+11196G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525150 | ||||||
| chr6:17525222
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(95): Show | 98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+11268T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525222 | ||||||
| chr6:17525240
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.636+11286A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525240 | ||||||
| chr6:17525372
|
G | A | 2 | a0001c0003t0002g0047a0005c0015t0001g0070 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.636+11418G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525372 | ||||||
| chr6:17525388
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(95): Show | 98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+11434T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525388 | ||||||
| chr6:17525394
|
G | A | 2 | a0001c0003t0002g0047a0005c0015t0001g0070 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.636+11440G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525394 | ||||||
| chr6:17525410
|
G | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0163 | 2 | NA18992.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.636+11456G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525410 | ||||||
| chr6:17525445
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.636+11491G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525445 | ||||||
| chr6:17525468
|
C | CA | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(86): Show | 89 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.636+11526dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17525468 | |||||
| chr6:17525551
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(170): Show | 173 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.636+11597A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525551 | ||||||
| chr6:17525736
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(95): Show | 98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+11782G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525736 | ||||||
| chr6:17525786
|
T | G | 5 | a0001c0001t0002g0050a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG01255.hp1 HG02486.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.636+11832T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525786 | ||||||
| chr6:17525865
|
G | A | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.636+11911G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525865 | ||||||
| chr6:17525869
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0140a0001c0001t0001g0142others(2): Show | 5 | HG01168.hp1 HG01168.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+11915G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525869 | ||||||
| chr6:17526029
|
G | T | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.636+12075G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526029 | ||||||
| chr6:17526082
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.636+12128G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526082 | ||||||
| chr6:17526085
|
C | G | 1 | a0001c0001t0001g0154 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.636+12131C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526085 | ||||||
| chr6:17526110
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.636+12156G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526110 | ||||||
| chr6:17526150
|
C | T | 1 | a0001c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.636+12196C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526150 | ||||||
| chr6:17526262
|
C | T | 1 | a0001c0003t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+12308C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526262 | ||||||
| chr6:17526263
|
A | G | 1 | a0001c0003t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+12309A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526263 | ||||||
| chr6:17526264
|
C | T | 1 | a0001c0003t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+12310C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526264 | ||||||
| chr6:17526266
|
C | T | 1 | a0001c0003t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+12312C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526266 | ||||||
| chr6:17526274
|
T | C | 1 | a0001c0003t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+12320T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526274 | ||||||
| chr6:17526280
|
A | G | 1 | a0001c0003t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+12326A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526280 | ||||||
| chr6:17526359
|
C | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.636+12405C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526359 | ||||||
| chr6:17526361
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(95): Show | 98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+12407A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526361 | ||||||
| chr6:17526369
|
G | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(95): Show | 98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+12415G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526369 | ||||||
| chr6:17526639
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-12630A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526639 | ||||||
| chr6:17526935
|
C | T | 2 | a0001c0003t0002g0047a0005c0015t0001g0070 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.637-12334C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526935 | ||||||
| chr6:17526956
|
C | CA | 101 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0018others(98): Show | 101 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.637-12291dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17526956 | |||||
| chr6:17526956
|
C | CAA | 21 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(18): Show | 21 | HG00438.hp1 HG01361.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.637-12292_637-1229 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17526956 | |||||
| chr6:17526956
|
C | CAAA | 19 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(16): Show | 19 | HG01106.hp2 HG01243.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.637-12293_637-1229 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17526956 | |||||
| chr6:17526956
|
CA | C | 5 | a0001c0001t0002g0050a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG01255.hp1 HG02486.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-12291delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17526956 | |||||
| chr6:17526969
|
A | AAAAG | 15 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.637-12297_637-1229 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17526969 | |||||
| chr6:17527172
|
C | A | 1 | a0001c0006t0001g0120 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.637-12097C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527172 | ||||||
| chr6:17527293
|
G | A | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.637-11976G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527293 | ||||||
| chr6:17527597
|
C | CT | 61 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0048others(58): Show | 61 | HG00438.hp2 HG00597.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.637-11655dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17527597 | |||||
| chr6:17527597
|
C | CTT | 43 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(40): Show | 43 | HG00438.hp1 HG00741.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.637-11656_637-1165 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17527597 | |||||
| chr6:17527597
|
C | CTTT | 26 | a0001c0001t0001g0018a0001c0001t0001g0124a0001c0001t0002g0150others(23): Show | 26 | HG00597.hp1 HG00735.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.637-11657_637-1165 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17527597 | |||||
| chr6:17527597
|
C | CTTTT | 6 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG01109.hp2 HG01891.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-11658_637-1165 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17527597 | |||||
| chr6:17527597
|
C | CTTTTT | 19 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(16): Show | 19 | HG01106.hp2 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.637-11659_637-1165 others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17527597 | |||||
| chr6:17527636
|
G | A | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0013t0001g0092 | 3 | HG02055.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.637-11633G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527636 | ||||||
| chr6:17527755
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(95): Show | 98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.637-11514T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527755 | ||||||
| chr6:17527892
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.637-11377T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527892 | ||||||
| chr6:17527919
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(95): Show | 98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.637-11350C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527919 | ||||||
| chr6:17527958
|
A | C | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.637-11311A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527958 | ||||||
| chr6:17528112
|
C | G | 1 | a0002c0004t0001g0089 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.637-11157C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528112 | ||||||
| chr6:17528189
|
C | G | 1 | a0001c0009t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.637-11080C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528189 | ||||||
| chr6:17528209
|
C | T | 80 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(77): Show | 80 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.637-11060C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528209 | ||||||
| chr6:17528213
|
G | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(15): Show | 18 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.637-11056G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528213 | ||||||
| chr6:17528235
|
A | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0041 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.637-11034A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528235 | ||||||
| chr6:17528284
|
G | A | 1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.637-10985G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528284 | ||||||
| chr6:17528619
|
G | T | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.637-10650G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528619 | ||||||
| chr6:17528664
|
G | A | 1 | a0001c0002t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.637-10605G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528664 | ||||||
| chr6:17528964
|
C | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-10305C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528964 | ||||||
| chr6:17528967
|
G | A | 27 | a0001c0001t0001g0069a0001c0002t0001g0002a0001c0002t0001g0019others(24): Show | 27 | HG01361.hp2 HG01496.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.637-10302G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528967 | ||||||
| chr6:17528992
|
G | A | 5 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(2): Show | 5 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-10277G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528992 | ||||||
| chr6:17529052
|
CA | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(51): Show | 54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-10207delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529052 | |||||
| chr6:17529111
|
T | C | 7 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 7 | HG01891.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.637-10158T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529111 | ||||||
| chr6:17529176
|
T | G | 32 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(29): Show | 32 | HG00438.hp1 HG00741.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.637-10093T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529176 | ||||||
| chr6:17529220
|
A | G | 9 | a0001c0002t0001g0058a0001c0003t0001g0038a0001c0003t0001g0084others(6): Show | 9 | HG00642.hp1 HG02109.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-10049A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529220 | ||||||
| chr6:17529223
|
T | G | 1 | a0001c0001t0001g0016 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.637-10046T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529223 | ||||||
| chr6:17529357
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(51): Show | 54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-9912T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529357 | ||||||
| chr6:17529361
|
T | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(51): Show | 54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-9908T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529361 | ||||||
| chr6:17529416
|
C | T | 1 | a0002c0004t0001g0089 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.637-9853C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529416 | ||||||
| chr6:17529417
|
G | A | 5 | a0001c0001t0002g0050a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG01255.hp1 HG02486.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-9852G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529417 | ||||||
| chr6:17529469
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(63): Show | 66 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.637-9800A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529469 | ||||||
| chr6:17529610
|
C | T | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.637-9659C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529610 | ||||||
| chr6:17529618
|
G | A | 2 | a0001c0003t0002g0047a0005c0015t0001g0070 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.637-9651G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529618 | ||||||
| chr6:17529638
|
C | T | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.637-9631C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529638 | ||||||
| chr6:17529640
|
C | CA | 15 | a0001c0001t0001g0008a0001c0001t0001g0039a0001c0001t0001g0044others(12): Show | 15 | HG00099.hp1 HG00597.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.637-9617dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529640 | |||||
| chr6:17529640
|
C | CAA | 26 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0016others(23): Show | 26 | HG00438.hp1 HG00741.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.637-9618_637-9617d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529640 | |||||
| chr6:17529640
|
C | CAAAAAA | 6 | a0001c0001t0001g0083a0001c0001t0001g0086a0003c0007t0001g0059others(3): Show | 6 | HG01106.hp2 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-9622_637-9617d others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529640 | |||||
| chr6:17529640
|
C | CAAAAAAA | 10 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0068others(7): Show | 10 | HG01109.hp2 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.637-9623_637-9617d others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529640 | |||||
| chr6:17529640
|
C | CAAAAAAA others(4): Show |
4 | a0001c0003t0001g0065a0001c0003t0001g0082a0001c0003t0001g0088others(1): Show | 4 | HG01496.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-9627_637-9617d others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529640 | |||||
| chr6:17529640
|
CA | C | 11 | a0002c0004t0001g0089a0002c0004t0002g0077a0002c0004t0002g0079others(8): Show | 11 | HG00597.hp1 HG00735.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.637-9617delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529640 | |||||
| chr6:17529651
|
A | AAAAAAAA others(7): Show |
1 | a0001c0002t0001g0062 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.637-9617_637-9616i others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | |||||
| chr6:17529651
|
A | AAAAAAAA others(4): Show |
2 | a0001c0002t0002g0115a0001c0002t0006g0133 | 2 | HG01952.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.637-9617_637-9616i others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | |||||
| chr6:17529651
|
A | AAAAAAAA others(5): Show |
2 | a0001c0002t0001g0019a0001c0014t0008g0015 | 2 | HG01361.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.637-9617_637-9616i others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | |||||
| chr6:17529651
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.637-9617_637-9616i others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | |||||
| chr6:17529651
|
A | AAAAAAAA others(4): Show |
11 | a0001c0002t0001g0072a0001c0002t0001g0108a0001c0002t0002g0073others(8): Show | 11 | HG01517.hp1 HG01928.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.637-9617_637-9616i others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | |||||
| chr6:17529651
|
A | AAAAAAAA others(3): Show |
1 | a0001c0002t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.637-9617_637-9616i others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | |||||
| chr6:17529651
|
A | AAAAAAAA others(5): Show |
2 | a0001c0008t0001g0204a0006c0016t0001g0194 | 2 | HG02055.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.637-9617_637-9616i others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | |||||
| chr6:17529651
|
A | AAAAAAAT others(4): Show |
1 | a0001c0002t0001g0071 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.637-9617_637-9616i others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | |||||
| chr6:17529651
|
A | AAAAAAAT others(10): Show |
1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.637-9617_637-9616i others(19): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | |||||
| chr6:17529651
|
A | AAAT | 9 | a0001c0001t0001g0099a0001c0001t0001g0103a0001c0003t0001g0038others(6): Show | 9 | HG02109.hp1 HG02647.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-9617_637-9616i others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | |||||
| chr6:17529651
|
A | ATAT | 2 | a0001c0002t0001g0058a0001c0008t0001g0057 | 2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.637-9618_637-9617i others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529651 | ||||||
| chr6:17529651
|
A | T | 4 | a0001c0002t0001g0006a0001c0002t0001g0109a0001c0002t0001g0173others(1): Show | 4 | HG01106.hp1 HG02027.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-9618A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529651 | ||||||
| chr6:17529652
|
AT | A | 4 | a0001c0001t0002g0042a0001c0001t0002g0046a0001c0001t0002g0176others(1): Show | 4 | HG01884.hp2 HG03017.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-9616delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529652 | ||||||
| chr6:17529653
|
T | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 89 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.637-9616T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529653 | ||||||
| chr6:17529655
|
T | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0036others(58): Show | 61 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.637-9614T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529655 | ||||||
| chr6:17529657
|
T | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0041a0003c0007t0001g0110others(1): Show | 4 | HG01106.hp2 HG01243.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-9612T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529657 | ||||||
| chr6:17529780
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.637-9489C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529780 | ||||||
| chr6:17529980
|
C | CA | 17 | a0001c0001t0002g0050a0001c0002t0001g0130a0001c0002t0001g0132others(14): Show | 17 | HG00597.hp1 HG00735.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.637-9276dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529980 | |||||
| chr6:17529980
|
CA | C | 5 | a0001c0001t0001g0069a0001c0002t0001g0002a0001c0002t0001g0062others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-9276delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529980 | |||||
| chr6:17530026
|
T | C | 1 | a0001c0002t0001g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.637-9243T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530026 | ||||||
| chr6:17530320
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(51): Show | 54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-8949G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530320 | ||||||
| chr6:17530386
|
G | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(51): Show | 54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-8883G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530386 | ||||||
| chr6:17530397
|
G | A | 29 | a0001c0001t0001g0069a0001c0002t0001g0002a0001c0002t0001g0019others(26): Show | 29 | HG01106.hp2 HG01243.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.637-8872G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530397 | ||||||
| chr6:17530476
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.637-8793G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530476 | ||||||
| chr6:17530635
|
T | C | 1 | a0001c0002t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.637-8634T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530635 | ||||||
| chr6:17530721
|
G | A | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.637-8548G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530721 | ||||||
| chr6:17530763
|
C | A | 1 | a0001c0002t0001g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.637-8506C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530763 | ||||||
| chr6:17530839
|
G | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.637-8430G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530839 | ||||||
| chr6:17531022
|
A | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(27): Show | 30 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.637-8247A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531022 | ||||||
| chr6:17531178
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(184): Show | 187 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.637-8091G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531178 | ||||||
| chr6:17531204
|
A | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(84): Show | 87 | HG00438.hp1 HG00741.hp1 HG01106.hp2 others(84): Show |
intron_variant | MODIFIER | c.637-8065A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531204 | ||||||
| chr6:17531353
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0158a0001c0001t0002g0168 | 3 | HG02083.hp1 HG02132.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.637-7916C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531353 | ||||||
| chr6:17531371
|
G | A | 2 | a0001c0003t0001g0084a0001c0003t0002g0131 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.637-7898G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531371 | ||||||
| chr6:17531430
|
T | C | 1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.637-7839T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531430 | ||||||
| chr6:17531590
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.637-7679A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531590 | ||||||
| chr6:17531679
|
G | T | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.637-7590G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531679 | ||||||
| chr6:17531710
|
A | G | 13 | a0001c0001t0002g0150a0002c0004t0001g0089a0002c0004t0002g0077others(10): Show | 13 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.637-7559A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531710 | ||||||
| chr6:17531733
|
G | A | 21 | a0001c0002t0001g0002a0001c0002t0001g0019a0001c0002t0001g0062others(18): Show | 21 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.637-7536G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531733 | ||||||
| chr6:17532025
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.637-7244A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532025 | ||||||
| chr6:17532037
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.637-7232C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532037 | ||||||
| chr6:17532134
|
C | CT | 14 | a0001c0001t0001g0028a0001c0001t0001g0124a0001c0001t0001g0179others(11): Show | 14 | HG00597.hp2 HG00741.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-7112dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17532134 | |||||
| chr6:17532134
|
CT | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0041others(42): Show | 45 | HG00438.hp1 HG01167.hp1 HG01517.hp1 others(42): Show |
intron_variant | MODIFIER | c.637-7112delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17532134 | |||||
| chr6:17532163
|
CAG | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(51): Show | 54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-7103_637-7102d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17532163 | |||||
| chr6:17532392
|
C | T | 1 | a0001c0001t0001g0004 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.637-6877C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532392 | ||||||
| chr6:17532430
|
C | G | 21 | a0001c0002t0001g0002a0001c0002t0001g0019a0001c0002t0001g0062others(18): Show | 21 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.637-6839C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532430 | ||||||
| chr6:17532432
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.637-6837C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532432 | ||||||
| chr6:17532511
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(51): Show | 54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-6758C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532511 | ||||||
| chr6:17532670
|
C | T | 1 | a0001c0003t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.637-6599C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532670 | ||||||
| chr6:17532703
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(51): Show | 54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-6566A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532703 | ||||||
| chr6:17532704
|
C | T | 1 | a0001c0002t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.637-6565C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532704 | ||||||
| chr6:17532727
|
G | A | 4 | a0001c0001t0001g0196a0001c0001t0002g0199a0001c0001t0005g0200others(1): Show | 4 | HG01891.hp1 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-6542G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532727 | ||||||
| chr6:17532734
|
C | T | 1 | a0001c0002t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.637-6535C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532734 | ||||||
| chr6:17532735
|
G | A | 8 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0086others(5): Show | 8 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.637-6534G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532735 | ||||||
| chr6:17532740
|
T | TC | 56 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0036others(53): Show | 56 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.637-6529_637-6528i others(3): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532740 | ||||||
| chr6:17532741
|
A | C | 89 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(86): Show | 89 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.637-6528A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532741 | ||||||
| chr6:17532750
|
A | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG01978.hp2 HG02735.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-6519A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532750 | ||||||
| chr6:17532752
|
C | A | 21 | a0001c0002t0001g0002a0001c0002t0001g0019a0001c0002t0001g0062others(18): Show | 21 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.637-6517C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532752 | ||||||
| chr6:17532754
|
C | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.637-6515C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532754 | ||||||
| chr6:17532764
|
A | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(49): Show | 52 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(49): Show |
intron_variant | MODIFIER | c.637-6505A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532764 | ||||||
| chr6:17532802
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(51): Show | 54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-6467G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532802 | ||||||
| chr6:17532839
|
A | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0052others(11): Show | 14 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-6430A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532839 | ||||||
| chr6:17532922
|
G | T | 2 | a0001c0002t0001g0130a0001c0002t0001g0132 | 2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.637-6347G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532922 | ||||||
| chr6:17532974
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.637-6295A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532974 | ||||||
| chr6:17533070
|
C | A | 1 | a0002c0004t0002g0097 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.637-6199C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17533070 | ||||||
| chr6:17533078
|
C | CAAAA | 17 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0086others(14): Show | 17 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.637-6174_637-6171d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17533078 | |||||
| chr6:17533078
|
C | CAAAAA | 24 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(21): Show | 24 | HG01517.hp1 HG01952.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.637-6175_637-6171d others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17533078 | |||||
| chr6:17533078
|
C | CAAAAAA | 11 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0002t0001g0002others(8): Show | 11 | HG01243.hp2 HG01891.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-6176_637-6171d others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17533078 | |||||
| chr6:17533078
|
CA | C | 136 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.637-6171delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17533078 | |||||
| chr6:17533214
|
TTAAA | T | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.637-6052_637-6049d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17533214 | |||||
| chr6:17533485
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.637-5784C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17533485 | ||||||
| chr6:17533572
|
C | CT | 46 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(43): Show | 46 | HG00438.hp1 HG00741.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.637-5682dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17533572 | |||||
| chr6:17533672
|
G | C | 14 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-5597G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17533672 | ||||||
| chr6:17533846
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.637-5423G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17533846 | ||||||
| chr6:17533895
|
C | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0103 | 2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.637-5374C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17533895 | ||||||
| chr6:17534008
|
A | G | 2 | a0001c0001t0002g0010a0001c0001t0002g0043 | 2 | HG01175.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.637-5261A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534008 | ||||||
| chr6:17534117
|
C | A | 1 | a0001c0014t0008g0015 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.637-5152C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534117 | ||||||
| chr6:17534220
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(89): Show | 92 | HG00438.hp1 HG00741.hp1 HG01106.hp2 others(89): Show |
intron_variant | MODIFIER | c.637-5049A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534220 | ||||||
| chr6:17534221
|
T | G | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.637-5048T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534221 | ||||||
| chr6:17534530
|
C | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(161): Show | 164 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.637-4739C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534530 | ||||||
| chr6:17534686
|
T | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.637-4583T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534686 | ||||||
| chr6:17534701
|
C | T | 54 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(51): Show | 54 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-4568C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534701 | ||||||
| chr6:17534788
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0052others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-4481T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534788 | ||||||
| chr6:17534895
|
C | T | 19 | a0001c0002t0001g0019a0001c0002t0001g0071a0001c0002t0001g0072others(16): Show | 19 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.637-4374C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534895 | ||||||
| chr6:17534947
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(28): Show | 31 | HG00438.hp1 HG00741.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.637-4322G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534947 | ||||||
| chr6:17534953
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(89): Show | 92 | HG00438.hp1 HG00741.hp1 HG01106.hp2 others(89): Show |
intron_variant | MODIFIER | c.637-4316A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534953 | ||||||
| chr6:17534972
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.637-4297G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534972 | ||||||
| chr6:17535116
|
T | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.637-4153T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535116 | ||||||
| chr6:17535223
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(89): Show | 92 | HG00438.hp1 HG00741.hp1 HG01106.hp2 others(89): Show |
intron_variant | MODIFIER | c.637-4046C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535223 | ||||||
| chr6:17535274
|
C | CT | 5 | a0001c0001t0001g0018a0001c0002t0001g0094a0001c0002t0001g0128others(2): Show | 5 | HG00609.hp2 HG01071.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-3978dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17535274 | |||||
| chr6:17535274
|
CT | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0052others(21): Show | 24 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.637-3978delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17535274 | |||||
| chr6:17535526
|
G | A | 54 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(51): Show | 54 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-3743G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535526 | ||||||
| chr6:17535553
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.637-3716C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535553 | ||||||
| chr6:17535563
|
C | T | 1 | a0001c0006t0001g0033 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.637-3706C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535563 | ||||||
| chr6:17535762
|
A | G | 52 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(49): Show | 52 | HG00438.hp1 HG00741.hp1 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.637-3507A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535762 | ||||||
| chr6:17535797
|
G | A | 13 | a0001c0001t0002g0150a0002c0004t0001g0089a0002c0004t0002g0077others(10): Show | 13 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.637-3472G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535797 | ||||||
| chr6:17535910
|
A | C | 4 | a0001c0002t0001g0130a0001c0002t0001g0132a0004c0010t0001g0063others(1): Show | 4 | HG01255.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-3359A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535910 | ||||||
| chr6:17536115
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.637-3154G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536115 | ||||||
| chr6:17536356
|
T | C | 8 | a0001c0003t0001g0038a0001c0003t0001g0084a0001c0003t0002g0060others(5): Show | 8 | HG02109.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.637-2913T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536356 | ||||||
| chr6:17536569
|
C | T | 14 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-2700C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536569 | ||||||
| chr6:17536766
|
C | T | 1 | a0001c0002t0006g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.637-2503C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536766 | ||||||
| chr6:17536811
|
G | A | 1 | a0006c0016t0001g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.637-2458G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536811 | ||||||
| chr6:17536866
|
T | C | 1 | a0002c0004t0002g0182 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.637-2403T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536866 | ||||||
| chr6:17536884
|
GA | G | 5 | a0001c0003t0001g0065a0001c0003t0001g0082a0001c0003t0001g0088others(2): Show | 5 | HG01361.hp2 HG01496.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-2384delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536884 | ||||||
| chr6:17537233
|
C | A | 2 | a0001c0002t0001g0188a0001c0002t0001g0189 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.637-2036C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537233 | ||||||
| chr6:17537237
|
GGTACAGT others(3): Show |
G | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.637-2029_637-2020d others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17537237 | |||||
| chr6:17537253
|
C | T | 5 | a0001c0003t0001g0065a0001c0003t0001g0082a0001c0003t0001g0088others(2): Show | 5 | HG01361.hp2 HG01496.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-2016C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537253 | ||||||
| chr6:17537270
|
T | G | 21 | a0001c0002t0001g0002a0001c0002t0001g0019a0001c0002t0001g0062others(18): Show | 21 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.637-1999T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537270 | ||||||
| chr6:17537325
|
T | C | 1 | a0001c0003t0002g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.637-1944T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537325 | ||||||
| chr6:17537500
|
A | ATGTTT | 19 | a0001c0002t0001g0019a0001c0002t0001g0071a0001c0002t0001g0072others(16): Show | 19 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.637-1752_637-1748d others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17537500 | |||||
| chr6:17537566
|
G | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(58): Show | 61 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.637-1703G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537566 | ||||||
| chr6:17537599
|
A | G | 14 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-1670A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537599 | ||||||
| chr6:17537602
|
CTGT | C | 14 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-1665_637-1663d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17537602 | |||||
| chr6:17537668
|
G | A | 14 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-1601G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537668 | ||||||
| chr6:17537747
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.637-1522G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537747 | ||||||
| chr6:17537791
|
C | T | 2 | a0001c0002t0001g0002a0001c0002t0001g0062 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.637-1478C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537791 | ||||||
| chr6:17537927
|
C | T | 2 | a0001c0002t0001g0005a0001c0002t0001g0153 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.637-1342C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537927 | ||||||
| chr6:17538023
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(160): Show | 163 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.637-1246T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17538023 | ||||||
| chr6:17538023
|
T | G | 1 | a0002c0004t0002g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.637-1246T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17538023 | ||||||
| chr6:17538376
|
C | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(58): Show | 61 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.637-893C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17538376 | ||||||
| chr6:17538704
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.637-565G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17538704 | ||||||
| chr6:17538941
|
A | G | 14 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-328A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17538941 | ||||||
| chr6:17539018
|
AGG | A | 12 | a0002c0004t0001g0089a0002c0004t0002g0077a0002c0004t0002g0079others(9): Show | 12 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.637-249_637-248del others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17539018 | |||||
| chr6:17539030
|
C | A | 2 | a0001c0002t0001g0093a0001c0002t0001g0094 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.637-239C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17539030 | ||||||
| chr6:17539047
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(161): Show | 164 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.637-222T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17539047 | ||||||
| chr6:17539090
|
G | C | 1 | a0001c0001t0002g0171 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.637-179G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17539090 | ||||||
| chr6:17539187
|
G | T | 53 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(50): Show | 53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.637-82G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17539187 | ||||||
| chr6:17539196
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.637-73G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17539196 | ||||||
| chr6:17539225
|
C | T | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.637-44C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17539225 | ||||||
| chr6:17540212
|
A | G | 106 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(103): Show | 106 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.826+754A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540212 | ||||||
| chr6:17540313
|
C | T | 19 | a0001c0002t0001g0019a0001c0002t0001g0071a0001c0002t0001g0072others(16): Show | 19 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.827-660C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540313 | ||||||
| chr6:17540345
|
G | A | 1 | a0002c0004t0002g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.827-628G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540345 | ||||||
| chr6:17540447
|
TA | T | 7 | a0001c0002t0001g0109a0001c0002t0001g0164a0001c0006t0001g0149others(4): Show | 7 | HG00438.hp2 HG02027.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.827-509delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 17540447 | |||||
| chr6:17540448
|
A | T | 1 | a0001c0003t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.827-525A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540448 | ||||||
| chr6:17540558
|
C | T | 15 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.827-415C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540558 | ||||||
| chr6:17540560
|
T | C | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.827-413T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540560 | ||||||
| chr6:17540613
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.827-360G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540613 | ||||||
| chr6:17540664
|
G | C | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.827-309G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540664 | ||||||
| chr6:17540669
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0052others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.827-304G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540669 | ||||||
| chr6:17541246
|
A | T | 14 | a0001c0003t0001g0038a0001c0003t0001g0065a0001c0003t0001g0082others(11): Show | 14 | HG01361.hp2 HG01496.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1002+98A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541246 | ||||||
| chr6:17541253
|
G | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0028others(106): Show | 109 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1002+105G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541253 | ||||||
| chr6:17541259
|
G | A | 71 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(68): Show | 71 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1002+111G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541259 | ||||||
| chr6:17541362
|
C | G | 12 | a0002c0004t0001g0089a0002c0004t0002g0077a0002c0004t0002g0079others(9): Show | 12 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1002+214C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541362 | ||||||
| chr6:17541377
|
C | T | 1 | a0001c0002t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1002+229C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541377 | ||||||
| chr6:17541400
|
T | G | 1 | a0001c0002t0001g0011 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1002+252T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541400 | ||||||
| chr6:17541436
|
C | T | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1002+288C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541436 | ||||||
| chr6:17541529
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1002+381G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541529 | ||||||
| chr6:17541673
|
G | C | 5 | a0001c0003t0001g0065a0001c0003t0001g0082a0001c0003t0001g0088others(2): Show | 5 | HG01361.hp2 HG01496.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002+525G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541673 | ||||||
| chr6:17541674
|
C | T | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1002+526C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541674 | ||||||
| chr6:17541726
|
AC | A | 54 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(51): Show | 54 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1002+581delC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 17541726 | |||||
| chr6:17541736
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1002+588G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541736 | ||||||
| chr6:17541742
|
G | A | 1 | a0001c0002t0002g0111 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1002+594G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541742 | ||||||
| chr6:17541766
|
T | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(34): Show | 37 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1002+618T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541766 | ||||||
| chr6:17541774
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0028others(103): Show | 106 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1002+626C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541774 | ||||||
| chr6:17541934
|
G | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(100): Show | 103 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1002+786G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541934 | ||||||
| chr6:17541962
|
T | C | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1002+814T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541962 | ||||||
| chr6:17541973
|
C | G | 1 | a0001c0001t0002g0096 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1002+825C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541973 | ||||||
| chr6:17542073
|
T | G | 100 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 100 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1003-764T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17542073 | ||||||
| chr6:17542156
|
G | C | 1 | a0001c0006t0001g0149 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1003-681G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17542156 | ||||||
| chr6:17542385
|
T | G | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(28): Show | 31 | HG00438.hp1 HG01167.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.1003-452T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17542385 | ||||||
| chr6:17542437
|
C | T | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1003-400C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17542437 | ||||||
| chr6:17542461
|
AC | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0040others(37): Show | 40 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.1003-374delC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 17542461 | |||||
| chr6:17542805
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(137): Show | 140 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1003-32A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17542805 | ||||||
| chr6:17543547
|
G | A | 1 | a0001c0011t0002g0081 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1209+404G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17543547 | ||||||
| chr6:17543612
|
A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.1209+469A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17543612 | ||||||
| chr6:17543624
|
C | CA | 8 | a0001c0001t0001g0076a0001c0002t0001g0090a0001c0002t0001g0101others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209+503dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17543624 | |||||
| chr6:17543624
|
CA | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0036others(28): Show | 31 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.1209+503delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17543624 | |||||
| chr6:17543624
|
CAA | C | 59 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0044others(56): Show | 59 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1209+502_1209+503d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17543624 | |||||
| chr6:17543624
|
CAAAAAAA others(7): Show |
C | 4 | a0001c0003t0001g0065a0001c0003t0001g0082a0001c0003t0001g0088others(1): Show | 4 | HG01496.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1209+490_1209+503d others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17543624 | |||||
| chr6:17543715
|
T | G | 50 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(47): Show | 50 | HG00438.hp1 HG01167.hp2 HG01192.hp1 others(47): Show |
intron_variant | MODIFIER | c.1209+572T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17543715 | ||||||
| chr6:17543723
|
T | G | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1209+580T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17543723 | ||||||
| chr6:17544120
|
G | A | 3 | a0001c0002t0001g0090a0001c0002t0001g0101a0001c0002t0001g0112 | 3 | HG01243.hp1 HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1209+977G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544120 | ||||||
| chr6:17544124
|
C | CA | 116 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1209+994dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17544124 | |||||
| chr6:17544124
|
C | CAA | 6 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0151others(3): Show | 6 | HG00438.hp2 HG02055.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1209+993_1209+994d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17544124 | |||||
| chr6:17544138
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.1209+995G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544138 | ||||||
| chr6:17544508
|
A | G | 2 | a0001c0002t0001g0002a0001c0002t0001g0062 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1209+1365A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544508 | ||||||
| chr6:17544544
|
C | CT | 71 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(68): Show | 71 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1209+1414dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17544544 | |||||
| chr6:17544664
|
T | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | HG01884.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1209+1521T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544664 | ||||||
| chr6:17544693
|
C | T | 4 | a0001c0003t0001g0065a0001c0003t0001g0082a0001c0003t0001g0088others(1): Show | 4 | HG01496.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1209+1550C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544693 | ||||||
| chr6:17544696
|
G | A | 8 | a0001c0003t0001g0038a0001c0003t0001g0084a0001c0003t0002g0060others(5): Show | 8 | HG02109.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209+1553G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544696 | ||||||
| chr6:17544741
|
G | T | 3 | a0003c0007t0001g0059a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1209+1598G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544741 | ||||||
| chr6:17544752
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1209+1609G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544752 | ||||||
| chr6:17544980
|
A | T | 1 | a0001c0001t0005g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1209+1837A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544980 | ||||||
| chr6:17545024
|
C | G | 27 | a0001c0002t0001g0002a0001c0002t0001g0019a0001c0002t0001g0062others(24): Show | 27 | HG01361.hp2 HG01496.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.1209+1881C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17545024 | ||||||
| chr6:17545278
|
G | A | 29 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(26): Show | 29 | HG00438.hp1 HG01167.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.1209+2135G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17545278 | ||||||
| chr6:17545278
|
G | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0028others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.1209+2135G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17545278 | ||||||
| chr6:17545376
|
T | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1209+2233T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17545376 | ||||||
| chr6:17545991
|
C | T | 14 | a0001c0001t0002g0050a0001c0001t0002g0150a0002c0004t0001g0089others(11): Show | 14 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1209+2848C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17545991 | ||||||
| chr6:17545995
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1209+2852A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17545995 | ||||||
| chr6:17546135
|
T | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1209+2992T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546135 | ||||||
| chr6:17546190
|
C | T | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1209+3047C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546190 | ||||||
| chr6:17546243
|
T | A | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1209+3100T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546243 | ||||||
| chr6:17546391
|
G | A | 1 | a0001c0002t0002g0167 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1209+3248G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546391 | ||||||
| chr6:17546483
|
G | A | 2 | a0004c0010t0001g0063a0004c0010t0002g0061 | 2 | HG01255.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1209+3340G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546483 | ||||||
| chr6:17546498
|
T | C | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1209+3355T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546498 | ||||||
| chr6:17546550
|
T | G | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1209+3407T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546550 | ||||||
| chr6:17546558
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1209+3415A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546558 | ||||||
| chr6:17546567
|
T | C | 1 | a0002c0004t0002g0077 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1209+3424T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546567 | ||||||
| chr6:17547011
|
A | T | 17 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(14): Show | 17 | HG01109.hp2 HG01255.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1209+3868A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547011 | ||||||
| chr6:17547116
|
A | G | 1 | a0001c0006t0001g0120 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1209+3973A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547116 | ||||||
| chr6:17547182
|
G | T | 3 | a0001c0002t0001g0002a0003c0007t0001g0066a0003c0007t0001g0205 | 3 | HG02258.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1209+4039G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547182 | ||||||
| chr6:17547280
|
A | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1209+4137A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547280 | ||||||
| chr6:17547357
|
C | T | 2 | a0001c0001t0002g0150a0002c0005t0001g0003 | 2 | HG02135.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1210-4107C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547357 | ||||||
| chr6:17547371
|
AT | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0140a0001c0001t0001g0142others(1): Show | 4 | HG01168.hp2 HG01975.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210-4091delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17547371 | |||||
| chr6:17547433
|
A | T | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1210-4031A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547433 | ||||||
| chr6:17547503
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1210-3961G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547503 | ||||||
| chr6:17547518
|
T | C | 2 | a0003c0007t0001g0110a0003c0007t0001g0119 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1210-3946T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547518 | ||||||
| chr6:17547557
|
A | G | 44 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0044others(41): Show | 44 | HG00099.hp1 HG00597.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1210-3907A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547557 | ||||||
| chr6:17547568
|
A | G | 4 | a0001c0002t0001g0058a0001c0008t0001g0051a0001c0008t0001g0057others(1): Show | 4 | HG00642.hp1 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210-3896A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547568 | ||||||
| chr6:17547571
|
G | C | 2 | a0001c0002t0001g0058a0001c0008t0001g0057 | 2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1210-3893G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547571 | ||||||
| chr6:17547584
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1210-3880G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547584 | ||||||
| chr6:17547596
|
T | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0154a0001c0001t0001g0178others(2): Show | 5 | HG01192.hp2 NA18612.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210-3868T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547596 | ||||||
| chr6:17547601
|
G | A | 1 | a0001c0002t0001g0173 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1210-3863G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547601 | ||||||
| chr6:17547608
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1210-3856A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547608 | ||||||
| chr6:17547630
|
C | A | 3 | a0001c0001t0001g0185a0001c0001t0002g0042a0001c0002t0001g0193 | 3 | HG00642.hp2 HG03017.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1210-3834C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547630 | ||||||
| chr6:17547637
|
T | C | 6 | a0001c0001t0001g0185a0001c0001t0002g0042a0001c0001t0007g0201others(3): Show | 6 | HG00642.hp2 HG01891.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210-3827T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547637 | ||||||
| chr6:17547644
|
A | G | 52 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0020others(49): Show | 52 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1210-3820A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547644 | ||||||
| chr6:17547648
|
T | C | 2 | a0001c0001t0002g0050a0001c0002t0001g0197 | 2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1210-3816T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547648 | ||||||
| chr6:17547652
|
T | C | 2 | a0001c0002t0001g0005a0001c0009t0001g0014 | 2 | HG03491.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1210-3812T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547652 | ||||||
| chr6:17547658
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1210-3806A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547658 | ||||||
| chr6:17547668
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.1210-3796T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547668 | ||||||
| chr6:17547701
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1210-3763C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547701 | ||||||
| chr6:17547723
|
C | G | 1 | a0001c0002t0001g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1210-3741C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547723 | ||||||
| chr6:17547809
|
T | C | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1210-3655T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547809 | ||||||
| chr6:17547840
|
C | CA | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(76): Show | 79 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.1210-3608dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17547840 | |||||
| chr6:17548061
|
A | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0009t0001g0012 | 3 | HG02145.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1210-3403A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548061 | ||||||
| chr6:17548105
|
T | C | 3 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0002t0001g0198 | 3 | HG02630.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1210-3359T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548105 | ||||||
| chr6:17548282
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1210-3182G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548282 | ||||||
| chr6:17548306
|
G | A | 44 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0026others(41): Show | 44 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1210-3158G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548306 | ||||||
| chr6:17548344
|
C | T | 1 | a0002c0004t0001g0089 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1210-3120C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548344 | ||||||
| chr6:17548361
|
G | C | 4 | a0001c0001t0002g0126a0001c0001t0002g0158a0001c0001t0002g0175others(1): Show | 4 | HG01981.hp1 NA18747.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210-3103G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548361 | ||||||
| chr6:17548511
|
G | C | 1 | a0002c0005t0004g0024 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1210-2953G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548511 | ||||||
| chr6:17548553
|
A | T | 1 | a0001c0001t0001g0048 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1210-2911A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548553 | ||||||
| chr6:17548699
|
G | T | 12 | a0001c0001t0001g0048a0001c0001t0001g0154a0001c0001t0001g0178others(9): Show | 12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1210-2765G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548699 | ||||||
| chr6:17548783
|
G | A | 3 | a0001c0003t0002g0060a0001c0003t0002g0064a0001c0003t0002g0087 | 3 | HG02109.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1210-2681G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548783 | ||||||
| chr6:17549191
|
C | T | 119 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 119 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1210-2273C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17549191 | ||||||
| chr6:17549201
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0178 | 2 | NA18612.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1210-2263C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17549201 | ||||||
| chr6:17549409
|
G | A | 2 | a0001c0001t0002g0050a0004c0010t0002g0061 | 2 | HG01255.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1210-2055G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17549409 | ||||||
| chr6:17549723
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1210-1741C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17549723 | ||||||
| chr6:17549725
|
A | G | 2 | a0001c0002t0001g0058a0001c0008t0001g0057 | 2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1210-1739A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17549725 | ||||||
| chr6:17549927
|
C | T | 77 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 77 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1210-1537C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17549927 | ||||||
| chr6:17550202
|
C | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 82 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1210-1262C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550202 | ||||||
| chr6:17550207
|
T | C | 1 | a0001c0002t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1210-1257T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550207 | ||||||
| chr6:17550246
|
A | AAAAT | 22 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0041others(19): Show | 22 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1210-1197_1210-119 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550246 | |||||
| chr6:17550390
|
C | T | 4 | a0001c0001t0001g0165a0001c0002t0001g0098a0001c0002t0001g0161others(1): Show | 4 | HG00609.hp1 NA18939.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210-1074C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550390 | ||||||
| chr6:17550394
|
C | CT | 38 | a0001c0001t0002g0021a0001c0001t0002g0031a0001c0001t0002g0042others(35): Show | 38 | HG00597.hp2 HG00735.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1210-1043dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550394 | |||||
| chr6:17550394
|
C | CTT | 17 | a0001c0001t0001g0048a0001c0001t0001g0069a0001c0001t0001g0178others(14): Show | 17 | HG00597.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1210-1044_1210-104 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550394 | |||||
| chr6:17550394
|
C | CTTT | 9 | a0001c0001t0001g0154a0001c0001t0001g0196a0001c0001t0002g0026others(6): Show | 9 | HG02135.hp2 HG03017.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1210-1045_1210-104 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550394 | |||||
| chr6:17550394
|
CT | C | 21 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0044others(18): Show | 21 | HG00099.hp1 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.1210-1043delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550394 | |||||
| chr6:17550394
|
CTTTT | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(8): Show | 11 | HG00438.hp1 HG00741.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1210-1046_1210-104 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550394 | |||||
| chr6:17550394
|
CTTTTT | C | 71 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(68): Show | 71 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1210-1047_1210-104 others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550394 | |||||
| chr6:17550434
|
A | G | 7 | a0001c0001t0001g0069a0001c0003t0001g0065a0001c0003t0001g0082others(4): Show | 7 | HG01496.hp2 HG02055.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1210-1030A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550434 | ||||||
| chr6:17550567
|
C | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 5 | HG01167.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210-897C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550567 | ||||||
| chr6:17550582
|
C | T | 4 | a0001c0003t0001g0065a0001c0003t0001g0082a0001c0003t0001g0088others(1): Show | 4 | HG01496.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210-882C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550582 | ||||||
| chr6:17550805
|
A | G | 1 | a0001c0013t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1210-659A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550805 | ||||||
| chr6:17550961
|
G | A | 8 | a0001c0001t0001g0052a0001c0002t0001g0058a0001c0002t0001g0090others(5): Show | 8 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1210-503G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550961 | ||||||
| chr6:17550985
|
A | G | 1 | a0001c0009t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1210-479A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550985 | ||||||
| chr6:17551146
|
A | G | 57 | a0001c0001t0002g0010a0001c0001t0002g0021a0001c0001t0002g0023others(54): Show | 57 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.1210-318A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17551146 | ||||||
| chr6:17551424
|
G | A | 1 | a0001c0001t0002g0172 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1210-40G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17551424 | ||||||
| chr6:17551765
|
C | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 82 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1350+161C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17551765 | ||||||
| chr6:17551999
|
T | G | 1 | a0001c0006t0001g0033 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1350+395T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17551999 | ||||||
| chr6:17552101
|
G | A | 1 | a0002c0004t0002g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1350+497G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552101 | ||||||
| chr6:17552150
|
C | G | 1 | a0001c0001t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1350+546C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552150 | ||||||
| chr6:17552269
|
T | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0154a0001c0001t0001g0178others(2): Show | 5 | HG01109.hp1 NA18612.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1350+665T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552269 | ||||||
| chr6:17552447
|
G | T | 1 | a0001c0006t0001g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1350+843G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552447 | ||||||
| chr6:17552449
|
G | A | 1 | a0001c0006t0001g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1350+845G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552449 | ||||||
| chr6:17552466
|
C | A | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1350+862C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552466 | ||||||
| chr6:17552569
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1350+965T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552569 | ||||||
| chr6:17552814
|
T | A | 1 | a0002c0004t0002g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1350+1210T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552814 | ||||||
| chr6:17552823
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1350+1219A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552823 | ||||||
| chr6:17552900
|
A | T | 1 | a0004c0010t0001g0063 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1350+1296A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552900 | ||||||
| chr6:17553127
|
A | G | 2 | a0001c0002t0001g0058a0001c0008t0001g0057 | 2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1350+1523A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553127 | ||||||
| chr6:17553188
|
A | C | 8 | a0001c0001t0001g0052a0001c0002t0001g0058a0001c0002t0001g0090others(5): Show | 8 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1350+1584A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553188 | ||||||
| chr6:17553201
|
G | A | 2 | a0001c0002t0001g0062a0001c0009t0001g0014 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1350+1597G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553201 | ||||||
| chr6:17553275
|
C | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 5 | HG01167.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1350+1671C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553275 | ||||||
| chr6:17553357
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0001g0154a0001c0001t0001g0178others(2): Show | 5 | HG01109.hp1 NA18612.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1350+1753G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553357 | ||||||
| chr6:17553376
|
TA | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.1350+1775delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 17553376 | |||||
| chr6:17553514
|
T | C | 3 | a0001c0001t0001g0052a0001c0002t0001g0058a0001c0008t0001g0057 | 3 | HG00642.hp1 HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1350+1910T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553514 | ||||||
| chr6:17553526
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.1350+1922A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553526 | ||||||
| chr6:17553544
|
A | C | 1 | a0002c0005t0001g0203 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1350+1940A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553544 | ||||||
| chr6:17553632
|
C | CA | 27 | a0001c0001t0001g0052a0001c0001t0001g0069a0001c0001t0001g0196others(24): Show | 27 | HG00438.hp2 HG00597.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1350+2044dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 17553632 | |||||
| chr6:17553644
|
A | C | 2 | a0001c0001t0002g0162a0001c0001t0002g0181 | 2 | NA18939.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1350+2040A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553644 | ||||||
| chr6:17553780
|
G | A | 1 | a0001c0003t0002g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1350+2176G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553780 | ||||||
| chr6:17553782
|
C | T | 59 | a0001c0001t0002g0010a0001c0001t0002g0021a0001c0001t0002g0023others(56): Show | 59 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1350+2178C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553782 | ||||||
| chr6:17553879
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(1): Show | 4 | HG02145.hp2 HG02258.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350+2275C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553879 | ||||||
| chr6:17553888
|
G | A | 1 | a0003c0007t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1350+2284G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553888 | ||||||
| chr6:17553889
|
C | G | 20 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0041others(17): Show | 20 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1350+2285C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553889 | ||||||
| chr6:17553979
|
T | C | 1 | a0001c0006t0001g0017 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1350+2375T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553979 | ||||||
| chr6:17554384
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1351-1975A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554384 | ||||||
| chr6:17554477
|
C | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0005g0200others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1351-1882C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554477 | ||||||
| chr6:17554507
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1351-1852A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554507 | ||||||
| chr6:17554668
|
G | A | 82 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 82 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1351-1691G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554668 | ||||||
| chr6:17554821
|
T | G | 1 | a0001c0001t0001g0004 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1351-1538T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554821 | ||||||
| chr6:17554871
|
G | C | 12 | a0001c0001t0001g0048a0001c0001t0001g0154a0001c0001t0001g0178others(9): Show | 12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1351-1488G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554871 | ||||||
| chr6:17554911
|
A | G | 1 | a0001c0014t0008g0015 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1351-1448A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554911 | ||||||
| chr6:17554936
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(1): Show | 4 | HG02145.hp2 HG02258.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351-1423G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554936 | ||||||
| chr6:17554940
|
G | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1351-1419G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554940 | ||||||
| chr6:17555025
|
A | G | 1 | a0001c0014t0008g0015 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1351-1334A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555025 | ||||||
| chr6:17555259
|
A | G | 1 | a0001c0003t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1351-1100A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555259 | ||||||
| chr6:17555277
|
C | T | 1 | a0001c0009t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1351-1082C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555277 | ||||||
| chr6:17555338
|
T | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1351-1021T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555338 | ||||||
| chr6:17555350
|
A | C | 1 | a0001c0001t0001g0178 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1351-1009A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555350 | ||||||
| chr6:17555355
|
C | T | 12 | a0001c0001t0001g0048a0001c0001t0001g0154a0001c0001t0001g0178others(9): Show | 12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1351-1004C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555355 | ||||||
| chr6:17555582
|
G | C | 1 | a0001c0006t0001g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1351-777G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555582 | ||||||
| chr6:17555666
|
C | T | 5 | a0001c0003t0001g0065a0001c0003t0001g0082a0001c0003t0001g0088others(2): Show | 5 | HG01496.hp2 HG02055.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1351-693C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555666 | ||||||
| chr6:17555731
|
T | C | 1 | a0001c0002t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1351-628T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555731 | ||||||
| chr6:17555746
|
T | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0041others(9): Show | 12 | HG00099.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1351-613T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555746 | ||||||
| chr6:17555930
|
G | A | 2 | a0001c0006t0001g0120a0001c0006t0001g0155 | 2 | HG02135.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1351-429G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555930 | ||||||
| chr6:17555970
|
G | A | 1 | a0001c0001t0002g0150 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1351-389G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555970 | ||||||
| chr6:17556053
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0067others(1): Show | 4 | HG02145.hp2 HG02258.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351-306C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17556053 | ||||||
| chr6:17556279
|
C | T | 12 | a0001c0001t0001g0048a0001c0001t0001g0154a0001c0001t0001g0178others(9): Show | 12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1351-80C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17556279 | ||||||
| chr6:17556296
|
A | G | 5 | a0001c0001t0001g0048a0001c0001t0001g0154a0001c0001t0001g0178others(2): Show | 5 | HG01109.hp1 NA18612.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1351-63A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17556296 |