| geneid | 23607 |
|---|---|
| ensemblid | ENSG00000198087.7 |
| hgncid | 14258 |
| symbol | CD2AP |
| name | CD2 associated protein |
| refseq_nuc | NM_012120.3 |
| refseq_prot | NP_036252.1 |
| ensembl_nuc | ENST00000359314.5 |
| ensembl_prot | ENSP00000352264.5 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 47477789 |
| end | 47627263 |
| strand | + |
| ver | v1.2 |
| region | chr6:47477789-47627263 |
| region5000 | chr6:47472789-47632263 |
| regionname0 | CD2AP_chr6_47477789_47627263 |
| regionname5000 | CD2AP_chr6_47472789_47632263 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 639 | 310 | 76 | 67 | 122 | 16 | 27 | 105 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0002 | 0/0 | 639 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0003 | 0/0 | 639 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0004 | 0/0 | 639 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0005 | 0/0 | 639 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0006 | 0/0 | 639 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0007 | 0/0 | 639 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1920 | 304 | 72 | 66 | 122 | 16 | 27 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| c0002 | 0/0 | 1920 | 6 | 5 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| c0003 | 1/0 | 1920 | 4 | 3 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| c0004 | 0/0 | 1920 | 2 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| c0005 | 0/0 | 1920 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| c0006 | 0/0 | 1920 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| c0007 | 0/0 | 1920 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| c0008 | 0/0 | 1920 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| c0009 | 0/0 | 1920 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| c0010 | 0/0 | 1920 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3489 | 47 | 8 | 14 | 17 | 4 | 3 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0002 | 0/0 | 3494 | 41 | 1 | 10 | 29 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0003 | 0/0 | 3496 | 12 | 1 | 3 | 8 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0004 | 0/0 | 3492 | 12 | 0 | 2 | 7 | 3 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0005 | 0/0 | 3493 | 11 | 0 | 2 | 8 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0006 | 0/0 | 3495 | 10 | 1 | 0 | 7 | 0 | 2 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0007 | 0/0 | 3496 | 8 | 0 | 3 | 5 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0008 | 0/0 | 3497 | 8 | 1 | 5 | 2 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0009 | 0/0 | 3492 | 7 | 1 | 1 | 3 | 1 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0010 | 0/0 | 3490 | 7 | 0 | 0 | 2 | 1 | 4 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0011 | 0/0 | 3491 | 6 | 0 | 1 | 1 | 0 | 4 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0012 | 1/0 | 3493 | 6 | 5 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0013 | 0/0 | 3498 | 6 | 2 | 1 | 1 | 2 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0014 | 0/0 | 3494 | 6 | 0 | 2 | 4 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0015 | 0/0 | 3495 | 5 | 0 | 0 | 5 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0016 | 0/0 | 3504 | 4 | 3 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0017 | 0/0 | 3488 | 4 | 1 | 0 | 3 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0018 | 0/0 | 3490 | 4 | 1 | 0 | 3 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0019 | 0/0 | 3492 | 4 | 1 | 0 | 3 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0020 | 0/0 | 3482 | 4 | 0 | 3 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0021 | 0/0 | 3489 | 3 | 3 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0022 | 0/0 | 3500 | 3 | 3 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0023 | 0/0 | 3497 | 3 | 3 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0024 | 0/0 | 3488 | 3 | 0 | 1 | 2 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0025 | 0/0 | 3494 | 3 | 0 | 0 | 2 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0026 | 0/0 | 3504 | 3 | 1 | 1 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0027 | 0/0 | 3494 | 2 | 1 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0028 | 0/0 | 3501 | 2 | 1 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0029 | 0/0 | 3502 | 2 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0030 | 0/0 | 3500 | 2 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0031 | 0/0 | 3504 | 2 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0032 | 0/0 | 3489 | 2 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0033 | 0/0 | 3495 | 2 | 1 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0034 | 0/0 | 3486 | 2 | 0 | 1 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0035 | 0/0 | 3490 | 2 | 1 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0036 | 0/0 | 3496 | 2 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0037 | 0/0 | 3494 | 2 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0038 | 0/0 | 3500 | 2 | 0 | 2 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0039 | 0/0 | 3492 | 2 | 0 | 0 | 0 | 0 | 2 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0040 | 0/0 | 3481 | 2 | 0 | 1 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0041 | 0/0 | 3493 | 2 | 0 | 1 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0042 | 0/0 | 3497 | 2 | 1 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0043 | 0/0 | 3493 | 2 | 0 | 2 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0044 | 0/0 | 3493 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0045 | 0/0 | 3491 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0046 | 0/0 | 3492 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0047 | 0/0 | 3496 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0048 | 0/0 | 3493 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0049 | 0/0 | 3489 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0050 | 0/0 | 3491 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0051 | 0/0 | 3489 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0052 | 0/0 | 3494 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0053 | 0/0 | 3493 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0054 | 0/0 | 3497 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0055 | 0/0 | 3495 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0056 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0057 | 0/0 | 3499 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0058 | 0/0 | 3492 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0059 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0060 | 0/0 | 3508 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0061 | 0/0 | 3493 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0062 | 0/0 | 3503 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0063 | 0/0 | 3505 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0064 | 0/0 | 3489 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0065 | 0/0 | 3493 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0066 | 0/0 | 3497 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0067 | 0/0 | 3499 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0068 | 0/0 | 3482 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0069 | 0/0 | 3482 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0070 | 0/0 | 3492 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0071 | 0/0 | 3491 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0072 | 0/0 | 3490 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0073 | 0/0 | 3494 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0074 | 0/0 | 3490 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0075 | 0/0 | 3496 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0076 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0077 | 0/0 | 3486 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0078 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0079 | 0/0 | 3492 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0080 | 0/0 | 3493 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0081 | 0/0 | 3494 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0082 | 0/0 | 3492 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0083 | 0/0 | 3490 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0084 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0085 | 0/0 | 3496 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0086 | 0/0 | 3502 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0087 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0088 | 0/0 | 3494 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0089 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0090 | 0/0 | 3502 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0091 | 0/0 | 3510 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0092 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0093 | 0/0 | 3494 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0094 | 0/0 | 3494 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0095 | 0/0 | 3469 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0096 | 0/0 | 3493 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0097 | 0/0 | 3495 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0098 | 0/0 | 3497 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0099 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0100 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| t0101 | 0/0 | 3501 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0228 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0307 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1920 | 304 | 72 | 66 | 122 | 16 | 27 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0003 | 1/0 | 1920 | 4 | 3 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0005 | 0/0 | 1920 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0008 | 0/0 | 1920 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0002c0002 | 0/0 | 1920 | 6 | 5 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0003c0004 | 0/0 | 1920 | 2 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0004c0006 | 0/0 | 1920 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0005c0007 | 0/0 | 1920 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0006c0010 | 0/0 | 1920 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0007c0009 | 0/0 | 1920 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5408 | 40 | 3 | 12 | 17 | 4 | 3 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0002 | 0/0 | 5413 | 41 | 1 | 10 | 29 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0003 | 0/0 | 5415 | 12 | 1 | 3 | 8 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0004 | 0/0 | 5411 | 12 | 0 | 2 | 7 | 3 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0005 | 0/0 | 5412 | 10 | 0 | 2 | 7 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0006 | 0/0 | 5414 | 10 | 1 | 0 | 7 | 0 | 2 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0007 | 0/0 | 5415 | 8 | 0 | 3 | 5 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0008 | 0/0 | 5416 | 8 | 1 | 5 | 2 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0009 | 0/0 | 5411 | 7 | 1 | 1 | 3 | 1 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0010 | 0/0 | 5409 | 7 | 0 | 0 | 2 | 1 | 4 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0011 | 0/0 | 5410 | 6 | 0 | 1 | 1 | 0 | 4 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0012 | 0/0 | 5412 | 3 | 3 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0013 | 0/0 | 5417 | 6 | 2 | 1 | 1 | 2 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0014 | 0/0 | 5413 | 6 | 0 | 2 | 4 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0015 | 0/0 | 5414 | 5 | 0 | 0 | 5 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0016 | 0/0 | 5423 | 4 | 3 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0017 | 0/0 | 5407 | 4 | 1 | 0 | 3 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0018 | 0/0 | 5409 | 4 | 1 | 0 | 3 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0019 | 0/0 | 5411 | 4 | 1 | 0 | 3 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0020 | 0/0 | 5401 | 4 | 0 | 3 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0021 | 0/0 | 5408 | 3 | 3 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0022 | 0/0 | 5419 | 3 | 3 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0023 | 0/0 | 5416 | 3 | 3 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0024 | 0/0 | 5407 | 3 | 0 | 1 | 2 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0025 | 0/0 | 5413 | 3 | 0 | 0 | 2 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0026 | 0/0 | 5423 | 3 | 1 | 1 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0027 | 0/0 | 5413 | 2 | 1 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0028 | 0/0 | 5420 | 2 | 1 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0029 | 0/0 | 5421 | 2 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0030 | 0/0 | 5419 | 2 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0031 | 0/0 | 5423 | 2 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0033 | 0/0 | 5414 | 2 | 1 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0034 | 0/0 | 5405 | 2 | 0 | 1 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0035 | 0/0 | 5409 | 2 | 1 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0036 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0037 | 0/0 | 5413 | 2 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0038 | 0/0 | 5419 | 2 | 0 | 2 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0039 | 0/0 | 5411 | 2 | 0 | 0 | 0 | 0 | 2 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0040 | 0/0 | 5400 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0041 | 0/0 | 5412 | 2 | 0 | 1 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0042 | 0/0 | 5416 | 2 | 1 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0043 | 0/0 | 5412 | 2 | 0 | 2 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0045 | 0/0 | 5410 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0046 | 0/0 | 5411 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0047 | 0/0 | 5415 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0048 | 0/0 | 5412 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0049 | 0/0 | 5408 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0050 | 0/0 | 5410 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0051 | 0/0 | 5408 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0052 | 0/0 | 5413 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0053 | 0/0 | 5412 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0054 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0055 | 0/0 | 5414 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0056 | 0/0 | 5417 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0057 | 0/0 | 5418 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0058 | 0/0 | 5411 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0059 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0060 | 0/0 | 5427 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0062 | 0/0 | 5422 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0063 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0064 | 0/0 | 5408 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0065 | 0/0 | 5412 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0066 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0067 | 0/0 | 5418 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0069 | 0/0 | 5401 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0070 | 0/0 | 5411 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0071 | 0/0 | 5410 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0072 | 0/0 | 5409 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0073 | 0/0 | 5413 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0074 | 0/0 | 5409 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0075 | 0/0 | 5415 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0076 | 0/0 | 5414 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0077 | 0/0 | 5405 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0078 | 0/0 | 5417 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0079 | 0/0 | 5411 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0080 | 0/0 | 5412 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0081 | 0/0 | 5413 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0082 | 0/0 | 5411 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0083 | 0/0 | 5409 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0084 | 0/0 | 5417 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0085 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0086 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0087 | 0/0 | 5417 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0088 | 0/0 | 5413 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0089 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0090 | 0/0 | 5421 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0091 | 0/0 | 5429 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0092 | 0/0 | 5417 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0093 | 0/0 | 5413 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0094 | 0/0 | 5413 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0095 | 0/0 | 5388 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0096 | 0/0 | 5412 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0097 | 0/0 | 5414 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0098 | 0/0 | 5416 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0100 | 0/0 | 5414 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0001t0101 | 0/0 | 5420 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0003t0012 | 1/0 | 5412 | 3 | 2 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0003t0044 | 0/0 | 5412 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0005t0068 | 0/0 | 5401 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0001c0008t0001 | 0/0 | 5408 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0002c0002t0001 | 0/0 | 5408 | 6 | 5 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0003c0004t0032 | 0/0 | 5408 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0003c0004t0061 | 0/0 | 5412 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0004c0006t0040 | 0/0 | 5400 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0005c0007t0005 | 0/0 | 5412 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0006c0010t0032 | 0/0 | 5408 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| a0007c0009t0099 | 0/0 | 5414 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | copy fasta | chr6 | 47472789 | 47632263 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0228 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0006g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0006g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0006g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0006g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0007g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0007g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0008g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0008g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0008g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0008g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0008g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0008g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0008g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0009g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0009g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0009g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0009g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0009g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0009g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0010g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0010g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0010g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0010g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0010g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0010g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0010g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0011g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0011g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0011g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0011g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0011g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0011g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0012g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0013g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0013g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0013g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0013g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0013g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0014g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0014g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0014g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0014g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0014g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0014g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0015g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0015g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0015g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0015g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0015g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0016g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0016g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0016g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0016g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0017g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0017g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0017g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0017g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0018g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0018g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0018g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0018g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0019g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0019g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0019g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0019g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0020g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0020g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0020g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0020g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0021g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0021g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0021g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0022g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0022g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0022g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0023g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0023g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0023g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0024g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0024g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0024g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0025g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0025g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0025g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0026g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0026g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0026g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0027g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0027g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0028g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0028g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0029g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0029g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0030g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0030g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0031g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0031g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0033g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0033g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0034g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0034g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0035g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0035g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0036g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0036g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0037g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0037g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0038g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0038g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0039g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0039g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0040g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0041g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0041g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0042g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0042g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0043g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0043g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0045g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0046g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0047g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0048g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0049g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0050g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0051g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0052g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0053g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0054g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0055g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0056g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0057g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0058g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0059g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0060g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0062g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0063g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0064g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0065g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0066g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0067g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0069g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0070g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0071g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0072g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0073g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0074g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0075g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0076g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0077g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0078g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0079g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0080g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0081g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0082g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0083g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0084g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0085g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0086g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0087g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0088g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0089g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0090g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0091g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0092g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0093g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0094g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0095g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0096g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0097g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0098g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0100g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0001t0101g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0003t0012g0307 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0003t0012g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0003t0012g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0003t0044g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0005t0068g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0001c0008t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0002c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0002c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0003c0004t0032g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0003c0004t0061g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0004c0006t0040g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0005c0007t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0006c0010t0032g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| a0007c0009t0099g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0101 | g0173 | EUR | GBR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | GBR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00140 | hp1 | a0001 | c0001 | t0009 | g0002 | EUR | GBR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0114 | EUR | GBR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00280 | hp2 | a0001 | c0001 | t0069 | g0100 | EUR | FIN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00323 | hp1 | a0001 | c0001 | t0045 | g0214 | EUR | FIN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00323 | hp2 | a0001 | c0001 | t0013 | g0013 | EUR | FIN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | CHS | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00423 | hp2 | a0001 | c0001 | t0009 | g0056 | EAS | CHS | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00438 | hp1 | a0001 | c0001 | t0018 | g0014 | EAS | CHS | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00438 | hp2 | a0001 | c0001 | t0014 | g0141 | EAS | CHS | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | CHS | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | CHS | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | CHS | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00639 | hp1 | a0001 | c0001 | t0014 | g0120 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00642 | hp2 | a0001 | c0001 | t0075 | g0010 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0099 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00735 | hp1 | a0001 | c0001 | t0020 | g0177 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00741 | hp1 | a0001 | c0001 | t0033 | g0204 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01069 | hp1 | a0001 | c0001 | t0008 | g0166 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01069 | hp2 | a0001 | c0001 | t0016 | g0295 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01071 | hp1 | a0001 | c0001 | t0082 | g0145 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0172 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0101 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01099 | hp2 | a0001 | c0001 | t0014 | g0133 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01106 | hp1 | a0001 | c0001 | t0008 | g0174 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01106 | hp2 | a0001 | c0001 | t0038 | g0054 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01168 | hp1 | a0001 | c0001 | t0043 | g0185 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01168 | hp2 | a0001 | c0001 | t0026 | g0016 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01169 | hp1 | a0001 | c0001 | t0043 | g0184 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0137 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01192 | hp2 | a0001 | c0001 | t0013 | g0059 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0276 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01243 | hp2 | a0001 | c0001 | t0040 | g0161 | AMR | PUR | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01255 | hp2 | a0001 | c0001 | t0055 | g0098 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01256 | hp2 | a0001 | c0001 | t0070 | g0009 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01257 | hp1 | a0001 | c0001 | t0024 | g0115 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01257 | hp2 | a0001 | c0001 | t0008 | g0169 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0170 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01261 | hp1 | a0001 | c0001 | t0041 | g0189 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01346 | hp1 | a0001 | c0001 | t0034 | g0140 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0271 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01358 | hp2 | a0001 | c0001 | t0097 | g0181 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01361 | hp2 | a0001 | c0001 | t0049 | g0282 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0241 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01433 | hp2 | a0001 | c0001 | t0038 | g0051 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0129 | EUR | IBS | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | IBS | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0144 | EUR | IBS | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01884 | hp1 | a0001 | c0001 | t0023 | g0203 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01884 | hp2 | a0001 | c0001 | t0088 | g0112 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01891 | hp1 | a0001 | c0001 | t0029 | g0289 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0310 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01928 | hp1 | a0001 | c0008 | t0001 | g0244 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01934 | hp2 | a0001 | c0001 | t0091 | g0005 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01943 | hp2 | a0001 | c0001 | t0020 | g0176 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01975 | hp2 | a0001 | c0001 | t0047 | g0124 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0123 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01981 | hp1 | a0001 | c0001 | t0027 | g0119 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01981 | hp2 | a0001 | c0001 | t0009 | g0022 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02055 | hp2 | a0001 | c0001 | t0084 | g0160 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0180 | EAS | KHV | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02056 | hp2 | a0001 | c0001 | t0011 | g0259 | EAS | KHV | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02135 | hp1 | a0001 | c0001 | t0025 | g0080 | EAS | KHV | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | KHV | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02148 | hp1 | a0001 | c0001 | t0046 | g0118 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02148 | hp2 | a0001 | c0001 | t0020 | g0175 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02165 | hp1 | a0007 | c0009 | t0099 | g0190 | EAS | CDX | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0260 | EAS | CDX | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02257 | hp1 | a0001 | c0003 | t0012 | g0309 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02257 | hp2 | a0001 | c0001 | t0078 | g0011 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02258 | hp1 | a0001 | c0001 | t0056 | g0299 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02258 | hp2 | a0001 | c0001 | t0021 | g0286 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02280 | hp1 | a0001 | c0001 | t0031 | g0297 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02280 | hp2 | a0001 | c0003 | t0044 | g0320 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02300 | hp2 | a0001 | c0001 | t0011 | g0231 | AMR | PEL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02451 | hp1 | a0001 | c0001 | t0023 | g0198 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02451 | hp2 | a0001 | c0001 | t0087 | g0102 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02523 | hp2 | a0001 | c0001 | t0006 | g0314 | EAS | KHV | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02602 | hp1 | a0001 | c0001 | t0095 | g0188 | SAS | PJL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02602 | hp2 | a0001 | c0001 | t0035 | g0109 | SAS | PJL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02615 | hp1 | a0001 | c0001 | t0035 | g0103 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0280 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02622 | hp1 | a0001 | c0001 | t0023 | g0202 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02622 | hp2 | a0001 | c0001 | t0059 | g0298 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02630 | hp1 | a0001 | c0001 | t0060 | g0294 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02630 | hp2 | a0001 | c0001 | t0028 | g0210 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02647 | hp1 | a0001 | c0001 | t0093 | g0117 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02647 | hp2 | a0001 | c0001 | t0092 | g0195 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0272 | SAS | PJL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02683 | hp2 | a0001 | c0001 | t0010 | g0108 | SAS | PJL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02717 | hp1 | a0001 | c0001 | t0019 | g0003 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02717 | hp2 | a0001 | c0001 | t0022 | g0290 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02723 | hp1 | a0001 | c0001 | t0037 | g0128 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02723 | hp2 | a0001 | c0001 | t0096 | g0165 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02809 | hp2 | a0001 | c0001 | t0057 | g0288 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0322 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02818 | hp2 | a0001 | c0001 | t0089 | g0050 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02886 | hp1 | a0001 | c0001 | t0013 | g0058 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02886 | hp2 | a0001 | c0001 | t0054 | g0211 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02895 | hp1 | a0001 | c0001 | t0065 | g0197 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02895 | hp2 | a0001 | c0001 | t0079 | g0104 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0167 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02922 | hp2 | a0001 | c0001 | t0086 | g0015 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02965 | hp1 | a0001 | c0001 | t0016 | g0291 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0278 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02970 | hp1 | a0001 | c0001 | t0016 | g0292 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02976 | hp1 | a0001 | c0001 | t0029 | g0293 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02976 | hp2 | a0001 | c0001 | t0022 | g0300 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03098 | hp1 | a0001 | c0001 | t0022 | g0305 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03098 | hp2 | a0001 | c0001 | t0053 | g0097 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03139 | hp1 | a0001 | c0001 | t0036 | g0159 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0279 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03195 | hp1 | a0001 | c0001 | t0037 | g0116 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03195 | hp2 | a0001 | c0001 | t0052 | g0301 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0201 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0296 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03225 | hp1 | a0001 | c0001 | t0033 | g0306 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03225 | hp2 | a0006 | c0010 | t0032 | g0313 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03453 | hp1 | a0001 | c0001 | t0085 | g0147 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03453 | hp2 | a0001 | c0001 | t0076 | g0206 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03486 | hp1 | a0003 | c0004 | t0032 | g0312 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03486 | hp2 | a0001 | c0001 | t0074 | g0162 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03491 | hp1 | a0001 | c0001 | t0039 | g0134 | SAS | PJL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03492 | hp1 | a0001 | c0001 | t0011 | g0253 | SAS | PJL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03492 | hp2 | a0001 | c0001 | t0039 | g0135 | SAS | PJL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03516 | hp1 | a0001 | c0005 | t0068 | g0001 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0095 | AFR | ESN | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03540 | hp1 | a0001 | c0001 | t0017 | g0004 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03579 | hp1 | a0001 | c0001 | t0042 | g0168 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03579 | hp2 | a0001 | c0001 | t0080 | g0207 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03669 | hp2 | a0001 | c0001 | t0041 | g0171 | SAS | PJL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03688 | hp1 | a0001 | c0001 | t0025 | g0057 | SAS | STU | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03688 | hp2 | a0001 | c0001 | t0028 | g0209 | SAS | STU | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03710 | hp1 | a0001 | c0001 | t0020 | g0194 | SAS | PJL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03710 | hp2 | a0004 | c0006 | t0040 | g0193 | SAS | PJL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03831 | hp1 | a0001 | c0001 | t0010 | g0150 | SAS | BEB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03831 | hp2 | a0001 | c0001 | t0009 | g0083 | SAS | BEB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03927 | hp1 | a0001 | c0001 | t0011 | g0265 | SAS | BEB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03927 | hp2 | a0001 | c0001 | t0010 | g0127 | SAS | BEB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0186 | SAS | BEB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG04115 | hp1 | a0001 | c0001 | t0010 | g0143 | SAS | STU | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG04184 | hp1 | a0001 | c0001 | t0006 | g0179 | SAS | BEB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG04184 | hp2 | a0001 | c0001 | t0011 | g0250 | SAS | BEB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG04199 | hp1 | a0001 | c0001 | t0011 | g0251 | SAS | STU | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG04199 | hp2 | a0001 | c0001 | t0094 | g0148 | SAS | STU | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG04228 | hp1 | a0001 | c0001 | t0051 | g0287 | SAS | STU | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG04228 | hp2 | a0001 | c0001 | t0058 | g0130 | SAS | STU | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0220 | EAS | CHB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18612 | hp2 | a0001 | c0001 | t0009 | g0065 | EAS | CHB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18906 | hp1 | a0001 | c0003 | t0012 | g0308 | AFR | YRI | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18906 | hp2 | a0001 | c0001 | t0026 | g0049 | AFR | YRI | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18939 | hp2 | a0001 | c0001 | t0008 | g0178 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0315 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18941 | hp2 | a0001 | c0001 | t0018 | g0055 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18942 | hp2 | a0001 | c0001 | t0010 | g0131 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18946 | hp2 | a0001 | c0001 | t0006 | g0317 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18953 | hp2 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18954 | hp1 | a0001 | c0001 | t0008 | g0182 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18954 | hp2 | a0001 | c0001 | t0017 | g0044 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18956 | hp1 | a0001 | c0001 | t0007 | g0153 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18956 | hp2 | a0001 | c0001 | t0072 | g0007 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18959 | hp1 | a0001 | c0001 | t0009 | g0020 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18959 | hp2 | a0001 | c0001 | t0014 | g0111 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18961 | hp2 | a0001 | c0001 | t0025 | g0024 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0318 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18967 | hp1 | a0001 | c0001 | t0010 | g0106 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18969 | hp2 | a0001 | c0001 | t0007 | g0122 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18970 | hp1 | a0001 | c0001 | t0014 | g0121 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18972 | hp1 | a0001 | c0001 | t0098 | g0191 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18975 | hp1 | a0001 | c0001 | t0050 | g0218 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18975 | hp2 | a0001 | c0001 | t0019 | g0061 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18977 | hp1 | a0001 | c0001 | t0062 | g0163 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18977 | hp2 | a0001 | c0001 | t0081 | g0079 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18980 | hp1 | a0001 | c0001 | t0015 | g0261 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18980 | hp2 | a0001 | c0001 | t0017 | g0042 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18981 | hp2 | a0001 | c0001 | t0007 | g0156 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0219 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18993 | hp2 | a0001 | c0001 | t0042 | g0192 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18998 | hp1 | a0001 | c0001 | t0024 | g0149 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18999 | hp2 | a0005 | c0007 | t0005 | g0224 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19000 | hp1 | a0001 | c0001 | t0006 | g0316 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19000 | hp2 | a0001 | c0001 | t0019 | g0084 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19004 | hp1 | a0001 | c0001 | t0017 | g0030 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19004 | hp2 | a0001 | c0001 | t0015 | g0262 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19006 | hp2 | a0001 | c0001 | t0015 | g0263 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19009 | hp1 | a0001 | c0001 | t0024 | g0142 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19011 | hp1 | a0001 | c0001 | t0063 | g0164 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19030 | hp1 | a0001 | c0001 | t0021 | g0229 | AFR | LWK | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19030 | hp2 | a0001 | c0001 | t0067 | g0196 | AFR | LWK | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19043 | hp1 | a0001 | c0001 | t0021 | g0230 | AFR | LWK | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19043 | hp2 | a0003 | c0004 | t0061 | g0311 | AFR | LWK | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19054 | hp1 | a0001 | c0001 | t0090 | g0154 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19054 | hp2 | a0001 | c0001 | t0019 | g0039 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0255 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19059 | hp1 | a0001 | c0001 | t0014 | g0151 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19060 | hp1 | a0001 | c0001 | t0013 | g0091 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0216 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19068 | hp1 | a0001 | c0001 | t0015 | g0264 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19068 | hp2 | a0001 | c0001 | t0018 | g0025 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19078 | hp1 | a0001 | c0001 | t0073 | g0075 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19086 | hp2 | a0001 | c0001 | t0015 | g0222 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19090 | hp2 | a0001 | c0001 | t0083 | g0157 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19091 | hp1 | a0001 | c0001 | t0100 | g0187 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19091 | hp2 | a0001 | c0001 | t0007 | g0155 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19240 | hp1 | a0001 | c0001 | t0066 | g0199 | AFR | YRI | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA19240 | hp2 | a0001 | c0001 | t0018 | g0082 | AFR | YRI | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA20129 | hp1 | a0001 | c0001 | t0036 | g0158 | AFR | ASW | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ASW | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA20752 | hp1 | a0001 | c0001 | t0026 | g0052 | EUR | TSI | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0132 | EUR | TSI | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA20805 | hp1 | a0001 | c0001 | t0013 | g0047 | EUR | TSI | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA20805 | hp2 | a0001 | c0001 | t0034 | g0107 | EUR | TSI | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0138 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02486 | hp1 | a0001 | c0001 | t0030 | g0302 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0281 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02559 | hp1 | a0001 | c0001 | t0048 | g0321 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG02559 | hp2 | a0001 | c0001 | t0077 | g0113 | AFR | ACB | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0277 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0048 | AFR | MSL | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG06807 | hp1 | a0001 | c0001 | t0071 | g0205 | AFR | USA | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| HG06807 | hp2 | a0001 | c0001 | t0030 | g0304 | AFR | USA | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA18955 | hp2 | a0001 | c0001 | t0007 | g0152 | EAS | JPT | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0200 | AFR | USA | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA20300 | hp2 | a0001 | c0001 | t0027 | g0126 | AFR | USA | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA21309 | hp1 | a0001 | c0001 | t0031 | g0303 | AFR | LWK | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| NA21309 | hp2 | a0001 | c0001 | t0064 | g0284 | AFR | LWK | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0228 | REF | REF | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0012 | g0307 | REF | REF | CD2AP_chr6_47472789_47632263 | CD2AP | chr6 | 47472789 | 47632263 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:47503337
|
G | A | 1 | a0004 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.62G>A | p.Arg21Gln | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/18 | 518/5412 | 62/1920 | 21/639 | chr6 | 47503337 | ||
| chr6:47533651
|
G | A | 1 | a0005 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.215G>A | p.Arg72Gln | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/18 | 671/5412 | 215/1920 | 72/639 | chr6 | 47533651 | ||
| chr6:47554677
|
A | G | 1 | a0007 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.452A>G | p.Asn151Ser | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/18 | 908/5412 | 452/1920 | 151/639 | chr6 | 47554677 | ||
| chr6:47595933
|
C | A | 1 | a0006 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1181C>A | p.Pro394Gln | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/18 | 1637/5412 | 1181/1920 | 394/639 | chr6 | 47595933 | ||
| chr6:47609233
|
T | A | 1 | a0002 | 6 | HG01243.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
missense_variant | MODERATE | c.1743T>A | p.Asn581Lys | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/18 | 2199/5412 | 1743/1920 | 581/639 | chr6 | 47609233 | ||
| chr6:47624205
|
A | G | 2 | a0003a0006 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.1898A>G | p.Lys633Arg | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 2354/5412 | 1898/1920 | 633/639 | chr6 | 47624205 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:47503317
|
T | C | 1 | a0001c0005 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.42T>C | p.His14His | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/18 | 498/5412 | 42/1920 | 14/639 | chr6 | 47503317 | ||
| chr6:47533655
|
A | G | 2 | a0003c0004a0006c0010 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.219A>G | p.Glu73Glu | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/18 | 675/5412 | 219/1920 | 73/639 | chr6 | 47533655 | ||
| chr6:47554672
|
C | T | 1 | a0001c0005 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.447C>T | p.Thr149Thr | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/18 | 903/5412 | 447/1920 | 149/639 | chr6 | 47554672 | ||
| chr6:47574218
|
C | T | 1 | a0001c0008 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.696C>T | p.Ser232Ser | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/18 | 1152/5412 | 696/1920 | 232/639 | chr6 | 47574218 | ||
| chr6:47580890
|
T | A | 1 | a0001c0005 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.1035T>A | p.Ala345Ala | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/18 | 1491/5412 | 1035/1920 | 345/639 | chr6 | 47580890 | ||
| chr6:47595956
|
C | T | 9 | a0001c0001a0001c0005a0001c0008others(6): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
synonymous_variant | LOW | c.1204C>T | p.Leu402Leu | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/18 | 1660/5412 | 1204/1920 | 402/639 | chr6 | 47595956 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:47477804
|
C | A | 1 | a0001c0003t0044 | 1 | HG02280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-441C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/18 | 441 | chr6 | 47477804 | |||||
| chr6:47477804
|
C | G | 16 | a0001c0001t0006a0001c0001t0008a0001c0001t0020others(13): Show | 38 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-441C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/18 | 441 | chr6 | 47477804 | |||||
| chr6:47477892
|
T | A | 1 | a0001c0001t0045 | 1 | HG00323.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-353T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/18 | chr6 | 47477892 | ||||||
| chr6:47477948
|
G | C | 3 | a0001c0001t0027a0001c0001t0046a0001c0001t0047 | 4 | HG01975.hp2 HG01981.hp1 HG02148.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-297G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/18 | 297 | chr6 | 47477948 | |||||
| chr6:47477954
|
G | C | 1 | a0001c0001t0048 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-291G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/18 | 291 | chr6 | 47477954 | |||||
| chr6:47477978
|
G | A | 1 | a0001c0001t0049 | 1 | HG01361.hp2 | 5_prime_UTR_variant | MODIFIER | c.-267G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/18 | 267 | chr6 | 47477978 | |||||
| chr6:47478033
|
C | T | 1 | a0001c0001t0093 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-212C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/18 | 212 | chr6 | 47478033 | |||||
| chr6:47478053
|
A | C | 66 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(63): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
5_prime_UTR_variant | MODIFIER | c.-192A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/18 | 192 | chr6 | 47478053 | |||||
| chr6:47478191
|
T | A | 99 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(96): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
5_prime_UTR_variant | MODIFIER | c.-54T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/18 | 54 | chr6 | 47478191 | |||||
| chr6:47478236
|
G | A | 1 | a0001c0001t0050 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-9G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/18 | 9 | chr6 | 47478236 | |||||
| chr6:47624387
|
A | G | 1 | a0001c0001t0092 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*160A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 160 | chr6 | 47624387 | |||||
| chr6:47624413
|
A | T | 3 | a0001c0001t0027a0001c0001t0046a0001c0001t0047 | 4 | HG01975.hp2 HG01981.hp1 HG02148.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*186A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 186 | chr6 | 47624413 | |||||
| chr6:47624534
|
T | C | 1 | a0001c0005t0068 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*307T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 307 | chr6 | 47624534 | |||||
| chr6:47624546
|
A | C | 1 | a0001c0001t0064 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*319A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 319 | chr6 | 47624546 | |||||
| chr6:47624592
|
GT | G | 78 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(75): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*367delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 367 | INFO_REALIGN_3_PRIME | chr6 | 47624592 | ||||
| chr6:47624679
|
C | CTG | 19 | a0001c0001t0002a0001c0001t0006a0001c0001t0014others(16): Show | 82 | HG00438.hp2 HG00597.hp2 HG00639.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*494_*495dupGT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 496 | INFO_REALIGN_3_PRIME | chr6 | 47624679 | ||||
| chr6:47624679
|
C | CTGTG | 11 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(8): Show | 38 | HG00558.hp2 HG00642.hp2 HG00733.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*492_*495dupGTGT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 496 | INFO_REALIGN_3_PRIME | chr6 | 47624679 | ||||
| chr6:47624679
|
C | CTGTGTG | 8 | a0001c0001t0013a0001c0001t0056a0001c0001t0057others(5): Show | 13 | HG00323.hp2 HG01192.hp2 HG02055.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*490_*495dupGTGTGT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 496 | INFO_REALIGN_3_PRIME | chr6 | 47624679 | ||||
| chr6:47624679
|
C | CTGTGTGT others(1): Show |
5 | a0001c0001t0022a0001c0001t0028a0001c0001t0030others(2): Show | 10 | HG00099.hp1 HG01106.hp2 HG01433.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*488_*495dupGTGTGT others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 496 | INFO_REALIGN_3_PRIME | chr6 | 47624679 | ||||
| chr6:47624679
|
C | CTGTGTGT others(3): Show |
4 | a0001c0001t0029a0001c0001t0062a0001c0001t0086others(1): Show | 5 | HG01891.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*486_*495dupGTGTGT others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 496 | INFO_REALIGN_3_PRIME | chr6 | 47624679 | ||||
| chr6:47624679
|
C | CTGTGTGT others(5): Show |
4 | a0001c0001t0016a0001c0001t0026a0001c0001t0031others(1): Show | 10 | HG01069.hp2 HG01168.hp2 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*484_*495dupGTGTGT others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 496 | INFO_REALIGN_3_PRIME | chr6 | 47624679 | ||||
| chr6:47624679
|
C | CTGTGTGT others(7): Show |
2 | a0001c0001t0059a0001c0001t0089 | 2 | HG02622.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*482_*495dupGTGTGT others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 496 | INFO_REALIGN_3_PRIME | chr6 | 47624679 | ||||
| chr6:47624679
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0060 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*480_*495dupGTGTGT others(10): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 496 | INFO_REALIGN_3_PRIME | chr6 | 47624679 | ||||
| chr6:47624679
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0091 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478_*495dupGTGTGT others(12): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 496 | INFO_REALIGN_3_PRIME | chr6 | 47624679 | ||||
| chr6:47624679
|
C | G | 1 | a0001c0001t0043 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*452C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 452 | chr6 | 47624679 | |||||
| chr6:47624679
|
CTG | C | 3 | a0001c0001t0011a0001c0001t0045a0001c0001t0050 | 8 | HG00323.hp1 HG02056.hp2 HG02300.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*494_*495delGT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 494 | INFO_REALIGN_3_PRIME | chr6 | 47624679 | ||||
| chr6:47624679
|
CTGTG | C | 5 | a0001c0001t0001a0001c0001t0049a0001c0001t0051others(2): Show | 49 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*492_*495delGTGT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 492 | INFO_REALIGN_3_PRIME | chr6 | 47624679 | ||||
| chr6:47624699
|
GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0095 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*474_*497delGTGTGT others(18): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 474 | INFO_REALIGN_3_PRIME | chr6 | 47624699 | ||||
| chr6:47624711
|
GTGTGTGT others(5): Show |
G | 3 | a0001c0001t0020a0001c0001t0040a0004c0006t0040 | 6 | HG00735.hp1 HG01243.hp2 HG01943.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*486_*497delGTGTGT others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 486 | INFO_REALIGN_3_PRIME | chr6 | 47624711 | ||||
| chr6:47624713
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0005t0068 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*488_*497delGTGTGT others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 488 | INFO_REALIGN_3_PRIME | chr6 | 47624713 | ||||
| chr6:47624719
|
GTGTA | G | 5 | a0001c0001t0017a0001c0001t0021a0001c0001t0064others(2): Show | 10 | HG02258.hp2 HG03225.hp2 HG03486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*494_*497delGTAT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 494 | INFO_REALIGN_3_PRIME | chr6 | 47624719 | ||||
| chr6:47624719
|
GTGTATAT others(3): Show |
G | 1 | a0001c0001t0069 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*494_*503delGTATAT others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 494 | INFO_REALIGN_3_PRIME | chr6 | 47624719 | ||||
| chr6:47624721
|
G | A | 1 | a0001c0001t0065 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 494 | chr6 | 47624721 | |||||
| chr6:47624721
|
G | GTGTA | 1 | a0001c0001t0023 | 3 | HG01884.hp1 HG02451.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*495_*496insGTAT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 496 | INFO_REALIGN_3_PRIME | chr6 | 47624721 | ||||
| chr6:47624721
|
GTA | G | 7 | a0001c0001t0010a0001c0001t0018a0001c0001t0035others(4): Show | 17 | HG00438.hp1 HG01516.hp1 HG02602.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*510_*511delAT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 510 | INFO_REALIGN_3_PRIME | chr6 | 47624721 | ||||
| chr6:47624721
|
GTATA | G | 1 | a0001c0001t0024 | 3 | HG01257.hp1 NA18998.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*508_*511delATAT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 508 | INFO_REALIGN_3_PRIME | chr6 | 47624721 | ||||
| chr6:47624721
|
GTATATA | G | 2 | a0001c0001t0034a0001c0001t0077 | 3 | HG01346.hp1 HG02559.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*506_*511delATATAT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 506 | INFO_REALIGN_3_PRIME | chr6 | 47624721 | ||||
| chr6:47624723
|
A | G | 59 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(56): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*496A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 496 | chr6 | 47624723 | |||||
| chr6:47624725
|
A | G | 34 | a0001c0001t0004a0001c0001t0007a0001c0001t0010others(31): Show | 76 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*498A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 498 | chr6 | 47624725 | |||||
| chr6:47624727
|
A | G | 23 | a0001c0001t0004a0001c0001t0007a0001c0001t0010others(20): Show | 58 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*500A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 500 | chr6 | 47624727 | |||||
| chr6:47624729
|
A | G | 17 | a0001c0001t0004a0001c0001t0007a0001c0001t0010others(14): Show | 51 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*502A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 502 | chr6 | 47624729 | |||||
| chr6:47624731
|
A | G | 4 | a0001c0001t0039a0001c0001t0077a0001c0001t0083others(1): Show | 5 | HG01884.hp2 HG02559.hp2 HG03491.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*504A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 504 | chr6 | 47624731 | |||||
| chr6:47624901
|
A | G | 1 | a0001c0001t0051 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*674A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 674 | chr6 | 47624901 | |||||
| chr6:47625310
|
A | G | 1 | a0001c0005t0068 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1083A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 1083 | chr6 | 47625310 | |||||
| chr6:47625649
|
A | G | 1 | a0001c0001t0074 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1422A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 1422 | chr6 | 47625649 | |||||
| chr6:47625721
|
T | C | 1 | a0001c0005t0068 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1494T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 1494 | chr6 | 47625721 | |||||
| chr6:47625933
|
T | C | 1 | a0001c0005t0068 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1706T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 1706 | chr6 | 47625933 | |||||
| chr6:47626234
|
C | T | 1 | a0001c0001t0080 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2007C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 2007 | chr6 | 47626234 | |||||
| chr6:47626266
|
T | C | 57 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(54): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*2039T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 2039 | chr6 | 47626266 | |||||
| chr6:47626447
|
A | AT | 22 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(19): Show | 90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2228dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 2229 | INFO_REALIGN_3_PRIME | chr6 | 47626447 | ||||
| chr6:47626468
|
A | T | 1 | a0001c0001t0082 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2241A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 2241 | chr6 | 47626468 | |||||
| chr6:47626566
|
T | C | 97 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(94): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*2339T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 2339 | chr6 | 47626566 | |||||
| chr6:47626599
|
A | G | 1 | a0001c0001t0039 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2372A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 2372 | chr6 | 47626599 | |||||
| chr6:47626986
|
G | A | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(15): Show | 94 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*2759G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 2759 | chr6 | 47626986 | |||||
| chr6:47627141
|
G | A | 1 | a0001c0001t0072 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2914G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 18/18 | 2914 | chr6 | 47627141 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:47478510
|
T | G | 96 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.4+262T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47478510 | ||||||
| chr6:47478606
|
C | T | 2 | a0001c0001t0012g0322a0001c0001t0048g0321 | 2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4+358C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47478606 | ||||||
| chr6:47478626
|
A | T | 1 | a0001c0003t0044g0320 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4+378A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47478626 | ||||||
| chr6:47478720
|
A | C | 1 | a0001c0001t0004g0319 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.4+472A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47478720 | ||||||
| chr6:47479025
|
T | C | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4+777T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47479025 | ||||||
| chr6:47479039
|
G | C | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4+791G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47479039 | ||||||
| chr6:47479045
|
A | G | 5 | a0001c0001t0006g0314a0001c0001t0006g0315a0001c0001t0006g0316others(2): Show | 5 | HG02523.hp2 NA18940.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.4+797A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47479045 | ||||||
| chr6:47479059
|
C | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4+811C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47479059 | ||||||
| chr6:47479140
|
A | G | 1 | a0001c0001t0008g0310 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4+892A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47479140 | ||||||
| chr6:47479305
|
T | A | 63 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.4+1057T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47479305 | ||||||
| chr6:47479434
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4+1186C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47479434 | ||||||
| chr6:47479674
|
T | A | 318 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.4+1426T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47479674 | ||||||
| chr6:47479679
|
C | T | 3 | a0001c0001t0036g0158a0001c0001t0036g0159a0001c0001t0084g0160 | 3 | HG02055.hp2 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4+1431C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47479679 | ||||||
| chr6:47479703
|
A | AT | 7 | a0001c0001t0007g0152a0001c0001t0007g0153a0001c0001t0007g0155others(4): Show | 7 | NA18955.hp2 NA18956.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.4+1456dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47479703 | |||||
| chr6:47479707
|
A | G | 17 | a0001c0001t0016g0291a0001c0001t0016g0292a0001c0001t0016g0295others(14): Show | 17 | HG01069.hp2 HG01891.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.4+1459A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47479707 | ||||||
| chr6:47479738
|
G | A | 1 | a0001c0001t0040g0161 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4+1490G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47479738 | ||||||
| chr6:47479823
|
T | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4+1575T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47479823 | ||||||
| chr6:47480094
|
C | T | 103 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(100): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.4+1846C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47480094 | ||||||
| chr6:47480145
|
T | G | 1 | a0001c0001t0001g0208 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.4+1897T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47480145 | ||||||
| chr6:47480151
|
A | G | 169 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.4+1903A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47480151 | ||||||
| chr6:47480177
|
T | G | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.4+1929T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47480177 | ||||||
| chr6:47480524
|
A | G | 17 | a0001c0001t0016g0291a0001c0001t0016g0292a0001c0001t0016g0295others(14): Show | 17 | HG01069.hp2 HG01891.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.4+2276A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47480524 | ||||||
| chr6:47480589
|
C | G | 3 | a0001c0001t0036g0158a0001c0001t0036g0159a0001c0001t0084g0160 | 3 | HG02055.hp2 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4+2341C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47480589 | ||||||
| chr6:47480600
|
A | G | 66 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(63): Show | 66 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.4+2352A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47480600 | ||||||
| chr6:47480733
|
G | GA | 39 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(36): Show | 39 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.4+2495dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47480733 | |||||
| chr6:47480864
|
A | G | 1 | a0001c0001t0057g0288 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4+2616A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47480864 | ||||||
| chr6:47480895
|
T | G | 1 | a0001c0001t0001g0208 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.4+2647T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47480895 | ||||||
| chr6:47481118
|
A | C | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4+2870A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47481118 | ||||||
| chr6:47481317
|
A | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4+3069A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47481317 | ||||||
| chr6:47481414
|
C | T | 1 | a0006c0010t0032g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4+3166C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47481414 | ||||||
| chr6:47481534
|
C | G | 1 | a0001c0001t0010g0150 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4+3286C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47481534 | ||||||
| chr6:47481574
|
G | A | 3 | a0001c0001t0007g0099a0001c0001t0007g0101a0001c0001t0069g0100 | 3 | HG00280.hp2 HG00733.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.4+3326G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47481574 | ||||||
| chr6:47481580
|
A | G | 1 | a0001c0001t0020g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4+3332A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47481580 | ||||||
| chr6:47481705
|
A | G | 1 | a0004c0006t0040g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4+3457A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47481705 | ||||||
| chr6:47481723
|
G | A | 1 | a0001c0001t0029g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4+3475G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47481723 | ||||||
| chr6:47481724
|
T | A | 1 | a0001c0001t0002g0096 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4+3476T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47481724 | ||||||
| chr6:47481846
|
A | G | 104 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(101): Show | 104 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.4+3598A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47481846 | ||||||
| chr6:47482084
|
T | C | 1 | a0001c0001t0087g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4+3836T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47482084 | ||||||
| chr6:47482191
|
T | G | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4+3943T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47482191 | ||||||
| chr6:47482380
|
C | CT | 9 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0094others(6): Show | 9 | HG01361.hp1 HG03225.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.4+4148dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47482380 | |||||
| chr6:47482472
|
G | A | 1 | a0001c0001t0009g0002 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4+4224G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47482472 | ||||||
| chr6:47482554
|
G | A | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.4+4306G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47482554 | ||||||
| chr6:47482581
|
T | C | 2 | a0001c0001t0017g0004a0001c0001t0019g0003 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4+4333T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47482581 | ||||||
| chr6:47482745
|
A | G | 306 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.4+4497A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47482745 | ||||||
| chr6:47482806
|
T | A | 5 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(2): Show | 5 | HG01934.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4+4558T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47482806 | ||||||
| chr6:47482861
|
G | A | 74 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.4+4613G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47482861 | ||||||
| chr6:47482882
|
G | A | 66 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(63): Show | 66 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.4+4634G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47482882 | ||||||
| chr6:47482947
|
T | C | 2 | a0001c0001t0035g0103a0001c0001t0079g0104 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.4+4699T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47482947 | ||||||
| chr6:47483139
|
A | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4+4891A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47483139 | ||||||
| chr6:47483277
|
A | G | 1 | a0001c0001t0021g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4+5029A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47483277 | ||||||
| chr6:47483352
|
G | C | 2 | a0001c0001t0062g0163a0001c0001t0063g0164 | 2 | NA18977.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.4+5104G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47483352 | ||||||
| chr6:47483353
|
G | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4+5105G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47483353 | ||||||
| chr6:47483384
|
G | A | 2 | a0001c0001t0004g0105a0001c0001t0010g0106 | 2 | NA18949.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.4+5136G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47483384 | ||||||
| chr6:47483792
|
G | GT | 38 | a0001c0001t0001g0208a0001c0001t0001g0283a0001c0001t0002g0087others(35): Show | 38 | HG01069.hp2 HG01261.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.4+5562dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47483792 | |||||
| chr6:47484054
|
T | G | 1 | a0001c0001t0022g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4+5806T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47484054 | ||||||
| chr6:47484147
|
C | T | 66 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(63): Show | 66 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.4+5899C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47484147 | ||||||
| chr6:47484179
|
T | C | 1 | a0001c0001t0004g0105 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.4+5931T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47484179 | ||||||
| chr6:47484351
|
CT | C | 167 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(164): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.4+6117delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47484351 | |||||
| chr6:47484363
|
T | G | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4+6115T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47484363 | ||||||
| chr6:47484370
|
T | C | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4+6122T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47484370 | ||||||
| chr6:47484408
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4+6160A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47484408 | ||||||
| chr6:47484499
|
A | T | 77 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.4+6251A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47484499 | ||||||
| chr6:47484532
|
A | G | 1 | a0001c0001t0024g0149 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.4+6284A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47484532 | ||||||
| chr6:47484534
|
T | C | 66 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(63): Show | 66 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.4+6286T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47484534 | ||||||
| chr6:47484670
|
G | C | 1 | a0001c0001t0072g0007 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.4+6422G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47484670 | ||||||
| chr6:47485280
|
T | G | 1 | a0003c0004t0061g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4+7032T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47485280 | ||||||
| chr6:47485350
|
A | G | 170 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.4+7102A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47485350 | ||||||
| chr6:47485566
|
TAGAA | T | 84 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(81): Show | 84 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.4+7328_4+7331delGA others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47485566 | |||||
| chr6:47485642
|
G | C | 65 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(62): Show | 65 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.4+7394G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47485642 | ||||||
| chr6:47485739
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4+7491G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47485739 | ||||||
| chr6:47485937
|
T | G | 1 | a0001c0001t0096g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4+7689T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47485937 | ||||||
| chr6:47485967
|
C | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4+7719C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47485967 | ||||||
| chr6:47486369
|
G | A | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4+8121G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47486369 | ||||||
| chr6:47486389
|
C | G | 1 | a0001c0001t0094g0148 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4+8141C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47486389 | ||||||
| chr6:47486427
|
CGA | C | 11 | a0001c0001t0006g0186a0001c0001t0041g0189a0001c0001t0043g0184others(8): Show | 11 | HG01168.hp1 HG01169.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.4+8189_4+8190delAG | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47486427 | |||||
| chr6:47486449
|
G | A | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.4+8201G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47486449 | ||||||
| chr6:47486562
|
ATACTGAG | A | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4+8320_4+8326delAG others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47486562 | |||||
| chr6:47486570
|
T | C | 1 | a0001c0001t0096g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4+8322T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47486570 | ||||||
| chr6:47486595
|
T | A | 68 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.4+8347T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47486595 | ||||||
| chr6:47486659
|
A | T | 38 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(35): Show | 38 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.4+8411A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47486659 | ||||||
| chr6:47486707
|
T | C | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4+8459T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47486707 | ||||||
| chr6:47486940
|
A | G | 1 | a0001c0001t0057g0288 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4+8692A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47486940 | ||||||
| chr6:47487159
|
T | C | 1 | a0002c0002t0001g0276 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4+8911T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47487159 | ||||||
| chr6:47487185
|
A | G | 2 | a0001c0001t0098g0191a0007c0009t0099g0190 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.4+8937A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47487185 | ||||||
| chr6:47487265
|
A | T | 1 | a0001c0001t0085g0147 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4+9017A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47487265 | ||||||
| chr6:47487416
|
C | T | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4+9168C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47487416 | ||||||
| chr6:47487418
|
C | T | 18 | a0001c0001t0013g0095a0001c0001t0016g0291a0001c0001t0016g0292others(15): Show | 18 | HG01069.hp2 HG01891.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.4+9170C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47487418 | ||||||
| chr6:47487438
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4+9190C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47487438 | ||||||
| chr6:47487461
|
C | T | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.4+9213C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47487461 | ||||||
| chr6:47487558
|
C | T | 1 | a0007c0009t0099g0190 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4+9310C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47487558 | ||||||
| chr6:47487563
|
G | A | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4+9315G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47487563 | ||||||
| chr6:47487583
|
G | A | 83 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.4+9335G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47487583 | ||||||
| chr6:47487604
|
G | A | 2 | a0001c0001t0010g0108a0001c0001t0034g0107 | 2 | HG02683.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.4+9356G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47487604 | ||||||
| chr6:47487646
|
C | T | 1 | a0001c0001t0096g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4+9398C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47487646 | ||||||
| chr6:47487690
|
A | AAAAC | 7 | a0001c0001t0001g0285a0001c0001t0002g0086a0001c0001t0021g0286others(4): Show | 7 | HG02258.hp2 HG02970.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.4+9466_4+9469dupCA others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47487690 | |||||
| chr6:47487690
|
AAAAC | A | 82 | a0001c0001t0001g0212a0001c0001t0004g0105a0001c0001t0004g0110others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.4+9466_4+9469delCA others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47487690 | |||||
| chr6:47488025
|
C | CT | 92 | a0001c0001t0001g0274a0001c0001t0001g0285a0001c0001t0004g0105others(89): Show | 92 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.4+9796dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47488025 | |||||
| chr6:47488025
|
CT | C | 8 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0006g0314others(5): Show | 8 | HG00099.hp2 HG00323.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.4+9796delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47488025 | |||||
| chr6:47488090
|
T | C | 7 | a0001c0001t0005g0216a0001c0001t0005g0217a0001c0001t0005g0219others(4): Show | 7 | NA18612.hp1 NA18953.hp2 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.4+9842T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47488090 | ||||||
| chr6:47488133
|
A | G | 92 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(89): Show | 92 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.4+9885A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47488133 | ||||||
| chr6:47488172
|
TATAA | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4+9930_4+9933delTA others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47488172 | |||||
| chr6:47488200
|
G | A | 2 | a0001c0001t0077g0113a0001c0001t0088g0112 | 2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.4+9952G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47488200 | ||||||
| chr6:47488329
|
G | A | 170 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.4+10081G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47488329 | ||||||
| chr6:47488382
|
A | G | 84 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.4+10134A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47488382 | ||||||
| chr6:47488412
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4+10164A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47488412 | ||||||
| chr6:47488536
|
T | C | 1 | a0001c0001t0004g0114 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4+10288T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47488536 | ||||||
| chr6:47488723
|
C | CA | 287 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.4+10490dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47488723 | |||||
| chr6:47488723
|
C | CAA | 19 | a0001c0001t0001g0223a0001c0001t0006g0315a0001c0001t0006g0316others(16): Show | 19 | HG00280.hp1 HG01069.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.4+10489_4+10490dup others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47488723 | |||||
| chr6:47488824
|
G | A | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4+10576G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47488824 | ||||||
| chr6:47488833
|
G | A | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4+10585G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47488833 | ||||||
| chr6:47488873
|
T | C | 3 | a0001c0001t0016g0292a0001c0001t0029g0293a0001c0001t0060g0294 | 3 | HG02630.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4+10625T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47488873 | ||||||
| chr6:47488936
|
T | A | 1 | a0001c0001t0002g0087 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4+10688T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47488936 | ||||||
| chr6:47489164
|
G | GT | 16 | a0001c0001t0002g0081a0001c0001t0002g0085a0001c0001t0002g0090others(13): Show | 16 | HG00140.hp1 HG01261.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.4+10939dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47489164 | |||||
| chr6:47489164
|
GTTTTTTT others(1): Show |
G | 90 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.4+10932_4+10939del others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47489164 | |||||
| chr6:47489164
|
GTTTTTTT others(2): Show |
G | 78 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(75): Show | 78 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.4+10931_4+10939del others(9): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47489164 | |||||
| chr6:47489164
|
GTTTTTTT others(3): Show |
G | 2 | a0003c0004t0032g0312a0003c0004t0061g0311 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4+10930_4+10939del others(10): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47489164 | |||||
| chr6:47489260
|
T | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4+11012T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47489260 | ||||||
| chr6:47489292
|
T | C | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.4+11044T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47489292 | ||||||
| chr6:47489504
|
G | A | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4+11256G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47489504 | ||||||
| chr6:47489584
|
A | C | 1 | a0001c0001t0001g0273 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4+11336A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47489584 | ||||||
| chr6:47489725
|
G | C | 170 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.4+11477G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47489725 | ||||||
| chr6:47489882
|
G | A | 1 | a0001c0001t0028g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4+11634G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47489882 | ||||||
| chr6:47489967
|
C | CT | 53 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0062others(50): Show | 53 | HG00558.hp2 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.4+11742dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47489967 | |||||
| chr6:47489967
|
C | CTT | 11 | a0001c0001t0004g0319a0001c0001t0028g0209a0001c0001t0028g0210others(8): Show | 11 | HG02630.hp2 HG02886.hp2 HG03225.hp2 others(8): Show |
intron_variant | MODIFIER | c.4+11741_4+11742dup others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47489967 | |||||
| chr6:47489967
|
CT | C | 8 | a0001c0001t0003g0012a0001c0001t0008g0166a0001c0001t0012g0322others(5): Show | 8 | HG00323.hp2 HG01069.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.4+11742delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47489967 | |||||
| chr6:47489967
|
CTTTTTTT others(3): Show |
C | 71 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0215others(68): Show | 71 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.4+11733_4+11742del others(10): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47489967 | |||||
| chr6:47489967
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0213 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.4+11732_4+11742del others(11): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47489967 | |||||
| chr6:47489971
|
T | TTG | 75 | a0001c0001t0004g0110a0001c0001t0004g0114a0001c0001t0004g0123others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.4+11724_4+11725ins others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47489971 | |||||
| chr6:47489972
|
T | TG | 3 | a0001c0001t0014g0151a0001c0001t0016g0295a0001c0001t0024g0115 | 3 | HG01069.hp2 HG01257.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.4+11724_4+11725ins others(1): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47489972 | ||||||
| chr6:47489978
|
T | G | 1 | a0001c0001t0016g0291 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4+11730T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47489978 | ||||||
| chr6:47490014
|
C | T | 1 | a0001c0001t0004g0146 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4+11766C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47490014 | ||||||
| chr6:47490052
|
A | T | 170 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.4+11804A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47490052 | ||||||
| chr6:47490231
|
A | T | 1 | a0001c0003t0044g0320 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4+11983A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47490231 | ||||||
| chr6:47490343
|
A | G | 1 | a0001c0001t0019g0061 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.4+12095A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47490343 | ||||||
| chr6:47490355
|
A | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4+12107A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47490355 | ||||||
| chr6:47491094
|
G | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5-12186G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47491094 | ||||||
| chr6:47491257
|
ATATGTGT others(5): Show |
A | 2 | a0001c0001t0010g0144a0001c0001t0082g0145 | 2 | HG01071.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.5-12009_5-11998del others(12): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47491257 | |||||
| chr6:47491259
|
A | ATG | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | NA18951.hp2 NA18986.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.5-12011_5-12010dup others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47491259 | |||||
| chr6:47491263
|
GTGTGTGT others(1): Show |
G | 3 | a0001c0001t0001g0285a0001c0001t0024g0115a0001c0001t0049g0282 | 3 | HG01257.hp1 HG01361.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5-12009_5-12002del others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47491263 | |||||
| chr6:47491265
|
GTGTGTA | G | 5 | a0001c0001t0001g0213a0001c0001t0001g0223a0001c0001t0001g0274others(2): Show | 5 | HG00280.hp1 HG00323.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.5-12009_5-12004del others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47491265 | |||||
| chr6:47491267
|
GTGTA | G | 55 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0215others(52): Show | 55 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.5-12009_5-12006del others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47491267 | |||||
| chr6:47491269
|
GTA | G | 9 | a0001c0001t0005g0260a0001c0001t0005g0272a0001c0001t0011g0265others(6): Show | 9 | HG01243.hp1 HG02165.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.5-12009_5-12008del others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47491269 | |||||
| chr6:47491271
|
A | ATG | 4 | a0001c0001t0008g0174a0001c0001t0008g0182a0001c0001t0100g0187others(1): Show | 4 | HG00099.hp1 HG01106.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.5-11977_5-11976dup others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47491271 | |||||
| chr6:47491271
|
A | G | 6 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(3): Show | 6 | HG01496.hp2 NA18951.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.5-12009A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47491271 | ||||||
| chr6:47491271
|
ATGTG | A | 3 | a0001c0001t0067g0196a0001c0005t0068g0001a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5-11979_5-11976del others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47491271 | |||||
| chr6:47491271
|
ATGTGTG | A | 6 | a0001c0001t0002g0060a0001c0001t0013g0059a0001c0001t0048g0321others(3): Show | 6 | HG01192.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.5-11981_5-11976del others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47491271 | |||||
| chr6:47491271
|
ATGTGTGT others(1): Show |
A | 117 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(114): Show | 117 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.5-11983_5-11976del others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47491271 | |||||
| chr6:47491271
|
ATGTGTGT others(3): Show |
A | 59 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(56): Show | 59 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.5-11985_5-11976del others(10): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47491271 | |||||
| chr6:47491271
|
ATGTGTGT others(5): Show |
A | 2 | a0001c0001t0037g0116a0001c0001t0093g0117 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5-11987_5-11976del others(12): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47491271 | |||||
| chr6:47491295
|
G | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5-11985G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47491295 | ||||||
| chr6:47491634
|
A | C | 2 | a0001c0001t0075g0010a0001c0001t0078g0011 | 2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.5-11646A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47491634 | ||||||
| chr6:47491726
|
C | T | 1 | a0001c0001t0007g0101 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.5-11554C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47491726 | ||||||
| chr6:47491788
|
T | G | 1 | a0001c0001t0071g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5-11492T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47491788 | ||||||
| chr6:47491823
|
T | A | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5-11457T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47491823 | ||||||
| chr6:47491824
|
A | T | 1 | a0001c0001t0078g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5-11456A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47491824 | ||||||
| chr6:47491869
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5-11411C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47491869 | ||||||
| chr6:47492165
|
C | T | 1 | a0001c0001t0014g0111 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.5-11115C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47492165 | ||||||
| chr6:47492347
|
C | CATTTT | 4 | a0001c0001t0020g0175a0001c0001t0020g0176a0001c0001t0020g0177others(1): Show | 4 | HG00735.hp1 HG01243.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.5-10933_5-10932ins others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47492347 | ||||||
| chr6:47492347
|
C | CT | 234 | a0001c0001t0001g0212a0001c0001t0001g0215a0001c0001t0001g0225others(231): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.5-10910dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47492347 | |||||
| chr6:47492347
|
C | CTT | 14 | a0001c0001t0001g0208a0001c0001t0002g0060a0001c0001t0002g0090others(11): Show | 14 | HG02056.hp2 HG02280.hp2 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.5-10911_5-10910dup others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47492347 | |||||
| chr6:47492373
|
G | T | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5-10907G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47492373 | ||||||
| chr6:47492592
|
C | T | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5-10688C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47492592 | ||||||
| chr6:47492593
|
G | A | 1 | a0001c0001t0010g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.5-10687G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47492593 | ||||||
| chr6:47492593
|
G | T | 1 | a0001c0003t0044g0320 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5-10687G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47492593 | ||||||
| chr6:47492674
|
A | G | 169 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.5-10606A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47492674 | ||||||
| chr6:47492855
|
A | C | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5-10425A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47492855 | ||||||
| chr6:47492946
|
A | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5-10334A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47492946 | ||||||
| chr6:47493067
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5-10213A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47493067 | ||||||
| chr6:47493168
|
A | G | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5-10112A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47493168 | ||||||
| chr6:47493175
|
T | C | 3 | a0001c0001t0036g0158a0001c0001t0036g0159a0001c0001t0084g0160 | 3 | HG02055.hp2 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.5-10105T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47493175 | ||||||
| chr6:47493261
|
G | T | 1 | a0006c0010t0032g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5-10019G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47493261 | ||||||
| chr6:47493324
|
A | G | 17 | a0001c0001t0016g0291a0001c0001t0016g0292a0001c0001t0016g0295others(14): Show | 17 | HG01069.hp2 HG01891.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.5-9956A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47493324 | ||||||
| chr6:47493354
|
G | GT | 259 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(256): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.5-9914dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47493354 | |||||
| chr6:47493354
|
G | GTT | 9 | a0001c0001t0001g0257a0001c0001t0003g0078a0001c0001t0022g0305others(6): Show | 9 | HG03098.hp1 HG03225.hp2 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.5-9915_5-9914dupTT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47493354 | |||||
| chr6:47493451
|
T | G | 1 | a0001c0001t0009g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5-9829T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47493451 | ||||||
| chr6:47493531
|
A | G | 169 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.5-9749A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47493531 | ||||||
| chr6:47493532
|
T | G | 1 | a0001c0001t0003g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5-9748T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47493532 | ||||||
| chr6:47493555
|
G | A | 1 | a0001c0001t0006g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5-9725G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47493555 | ||||||
| chr6:47493685
|
G | A | 1 | a0001c0001t0004g0319 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.5-9595G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47493685 | ||||||
| chr6:47493837
|
A | G | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.5-9443A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47493837 | ||||||
| chr6:47494177
|
C | A | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.5-9103C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47494177 | ||||||
| chr6:47494182
|
G | C | 17 | a0001c0001t0016g0291a0001c0001t0016g0292a0001c0001t0016g0295others(14): Show | 17 | HG01069.hp2 HG01891.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.5-9098G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47494182 | ||||||
| chr6:47494302
|
T | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5-8978T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47494302 | ||||||
| chr6:47494326
|
C | G | 2 | a0001c0001t0004g0319a0001c0001t0024g0142 | 2 | NA18968.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.5-8954C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47494326 | ||||||
| chr6:47494364
|
A | G | 1 | a0001c0001t0010g0150 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5-8916A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47494364 | ||||||
| chr6:47494400
|
G | A | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5-8880G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47494400 | ||||||
| chr6:47494545
|
T | C | 1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5-8735T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47494545 | ||||||
| chr6:47494562
|
G | A | 1 | a0001c0001t0007g0156 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.5-8718G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47494562 | ||||||
| chr6:47494723
|
T | C | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5-8557T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47494723 | ||||||
| chr6:47494835
|
G | A | 39 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(36): Show | 39 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.5-8445G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47494835 | ||||||
| chr6:47494879
|
T | C | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.5-8401T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47494879 | ||||||
| chr6:47495277
|
T | G | 1 | a0001c0001t0001g0225 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.5-8003T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47495277 | ||||||
| chr6:47495309
|
G | A | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.5-7971G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47495309 | ||||||
| chr6:47495390
|
G | T | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.5-7890G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47495390 | ||||||
| chr6:47495453
|
T | C | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5-7827T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47495453 | ||||||
| chr6:47495457
|
G | C | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5-7823G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47495457 | ||||||
| chr6:47495463
|
C | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0019 | 2 | HG00741.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.5-7817C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47495463 | ||||||
| chr6:47495594
|
C | T | 1 | a0001c0001t0014g0141 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5-7686C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47495594 | ||||||
| chr6:47495721
|
G | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5-7559G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47495721 | ||||||
| chr6:47495866
|
C | T | 77 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.5-7414C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47495866 | ||||||
| chr6:47495912
|
T | C | 3 | a0001c0001t0010g0144a0001c0001t0024g0115a0001c0001t0082g0145 | 3 | HG01071.hp1 HG01257.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.5-7368T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47495912 | ||||||
| chr6:47495918
|
A | G | 2 | a0001c0001t0010g0144a0001c0001t0024g0115 | 2 | HG01257.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.5-7362A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47495918 | ||||||
| chr6:47496116
|
T | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5-7164T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47496116 | ||||||
| chr6:47496228
|
T | C | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.5-7052T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47496228 | ||||||
| chr6:47496233
|
G | A | 1 | a0001c0001t0065g0197 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.5-7047G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47496233 | ||||||
| chr6:47496245
|
A | G | 2 | a0001c0001t0001g0256a0001c0001t0051g0287 | 2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.5-7035A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47496245 | ||||||
| chr6:47496292
|
T | G | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.5-6988T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47496292 | ||||||
| chr6:47496635
|
G | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5-6645G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47496635 | ||||||
| chr6:47497145
|
G | A | 77 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.5-6135G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497145 | ||||||
| chr6:47497147
|
G | GT | 83 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.5-6123dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47497147 | |||||
| chr6:47497148
|
T | G | 3 | a0001c0001t0006g0167a0001c0001t0008g0310a0001c0001t0042g0168 | 3 | HG01891.hp2 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5-6132T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497148 | ||||||
| chr6:47497201
|
C | T | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5-6079C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497201 | ||||||
| chr6:47497233
|
CTTTTCCT others(6): Show |
C | 82 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.5-6037_5-6025delTC others(11): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47497233 | |||||
| chr6:47497306
|
T | TTTTCC | 6 | a0001c0001t0002g0077a0001c0001t0002g0085a0001c0001t0003g0076others(3): Show | 6 | HG00423.hp2 HG02647.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.5-5948_5-5944dupTT others(3): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47497306 | |||||
| chr6:47497306
|
T | TTTTCCTT others(3): Show |
5 | a0001c0001t0006g0167a0001c0001t0008g0310a0003c0004t0032g0312others(2): Show | 5 | HG01891.hp2 HG02922.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.5-5953_5-5944dupTT others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47497306 | |||||
| chr6:47497321
|
C | CTTTCCTT others(3): Show |
81 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(78): Show | 81 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.5-5950_5-5949insAT others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47497321 | |||||
| chr6:47497331
|
C | A | 2 | a0001c0001t0005g0216a0001c0001t0005g0217 | 2 | NA18953.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.5-5949C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497331 | ||||||
| chr6:47497337
|
C | T | 4 | a0001c0001t0005g0216a0001c0001t0005g0217a0001c0001t0034g0140others(1): Show | 4 | HG01346.hp1 HG03579.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.5-5943C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497337 | ||||||
| chr6:47497341
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5-5939C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497341 | ||||||
| chr6:47497342
|
C | T | 2 | a0001c0001t0005g0216a0001c0001t0005g0217 | 2 | NA18953.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.5-5938C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497342 | ||||||
| chr6:47497347
|
C | CTCCCCT | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5-5912_5-5907dupCC others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47497347 | |||||
| chr6:47497347
|
C | CTCCCCTT others(5): Show |
2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5-5918_5-5907dupCC others(10): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47497347 | |||||
| chr6:47497347
|
CTCCCCT | C | 81 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(78): Show | 81 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.5-5912_5-5907delCC others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47497347 | |||||
| chr6:47497349
|
C | T | 4 | a0001c0001t0005g0216a0001c0001t0005g0217a0001c0001t0034g0140others(1): Show | 4 | HG01346.hp1 HG03579.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.5-5931C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497349 | ||||||
| chr6:47497358
|
C | T | 17 | a0001c0001t0016g0291a0001c0001t0016g0292a0001c0001t0016g0295others(14): Show | 17 | HG01069.hp2 HG01891.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.5-5922C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497358 | ||||||
| chr6:47497457
|
G | A | 4 | a0001c0001t0023g0198a0001c0001t0023g0202a0001c0001t0023g0203others(1): Show | 4 | HG00741.hp1 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.5-5823G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497457 | ||||||
| chr6:47497531
|
T | C | 82 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.5-5749T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497531 | ||||||
| chr6:47497619
|
G | T | 2 | a0003c0004t0032g0312a0003c0004t0061g0311 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5-5661G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497619 | ||||||
| chr6:47497625
|
G | C | 77 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.5-5655G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497625 | ||||||
| chr6:47497870
|
T | G | 11 | a0001c0001t0004g0123a0001c0001t0004g0125a0001c0001t0007g0122others(8): Show | 11 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.5-5410T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47497870 | ||||||
| chr6:47498262
|
CTT | C | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5-5015_5-5014delTT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47498262 | |||||
| chr6:47498513
|
C | T | 109 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(106): Show | 109 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.5-4767C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47498513 | ||||||
| chr6:47498548
|
T | A | 1 | a0001c0001t0009g0020 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.5-4732T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47498548 | ||||||
| chr6:47498657
|
G | C | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.5-4623G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47498657 | ||||||
| chr6:47498978
|
G | A | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5-4302G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47498978 | ||||||
| chr6:47499097
|
T | C | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.5-4183T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47499097 | ||||||
| chr6:47499115
|
G | C | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5-4165G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47499115 | ||||||
| chr6:47499123
|
A | G | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5-4157A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47499123 | ||||||
| chr6:47499144
|
T | C | 1 | a0001c0001t0002g0021 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.5-4136T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47499144 | ||||||
| chr6:47499307
|
A | ATG | 221 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.5-3955_5-3954dupGT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47499307 | |||||
| chr6:47499307
|
A | ATGTG | 16 | a0001c0001t0001g0228a0001c0001t0002g0006a0001c0001t0002g0008others(13): Show | 16 | HG01109.hp1 HG01255.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.5-3957_5-3954dupGT others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47499307 | |||||
| chr6:47499363
|
C | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5-3917C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47499363 | ||||||
| chr6:47499460
|
T | C | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5-3820T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47499460 | ||||||
| chr6:47499739
|
T | C | 1 | a0001c0001t0021g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5-3541T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47499739 | ||||||
| chr6:47499885
|
C | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.5-3395C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47499885 | ||||||
| chr6:47499889
|
C | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5-3391C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47499889 | ||||||
| chr6:47499898
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.5-3382T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47499898 | ||||||
| chr6:47499948
|
C | G | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5-3332C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47499948 | ||||||
| chr6:47500430
|
T | G | 1 | a0001c0001t0010g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5-2850T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47500430 | ||||||
| chr6:47500631
|
C | T | 1 | a0001c0001t0097g0181 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.5-2649C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47500631 | ||||||
| chr6:47500749
|
G | GT | 67 | a0001c0001t0001g0208a0001c0001t0001g0254a0001c0001t0004g0105others(64): Show | 67 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.5-2516dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47500749 | |||||
| chr6:47500776
|
C | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5-2504C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47500776 | ||||||
| chr6:47500823
|
T | C | 306 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.5-2457T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47500823 | ||||||
| chr6:47500940
|
G | A | 2 | a0001c0001t0021g0229a0001c0001t0021g0230 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.5-2340G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47500940 | ||||||
| chr6:47501282
|
T | C | 1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5-1998T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47501282 | ||||||
| chr6:47501366
|
G | A | 4 | a0001c0001t0022g0290a0001c0001t0022g0300a0001c0001t0052g0301others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.5-1914G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47501366 | ||||||
| chr6:47501400
|
G | A | 39 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(36): Show | 39 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.5-1880G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47501400 | ||||||
| chr6:47501423
|
C | T | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5-1857C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47501423 | ||||||
| chr6:47501537
|
A | G | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.5-1743A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47501537 | ||||||
| chr6:47501665
|
G | GGT | 4 | a0001c0001t0002g0046a0001c0001t0002g0090a0001c0001t0053g0097others(1): Show | 4 | HG01255.hp2 HG03098.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.5-1598_5-1597dupGT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47501665 | |||||
| chr6:47501665
|
GGT | G | 38 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(35): Show | 38 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.5-1598_5-1597delGT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47501665 | |||||
| chr6:47501779
|
A | G | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5-1501A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47501779 | ||||||
| chr6:47501824
|
A | G | 1 | a0001c0001t0011g0253 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.5-1456A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47501824 | ||||||
| chr6:47502032
|
G | C | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5-1248G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47502032 | ||||||
| chr6:47502145
|
A | T | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.5-1135A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47502145 | ||||||
| chr6:47502230
|
C | T | 1 | a0003c0004t0061g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5-1050C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47502230 | ||||||
| chr6:47502410
|
T | C | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.5-870T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47502410 | ||||||
| chr6:47502483
|
G | C | 1 | a0001c0001t0003g0067 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.5-797G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47502483 | ||||||
| chr6:47502493
|
G | GT | 25 | a0001c0001t0001g0212a0001c0001t0001g0252a0001c0001t0002g0021others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.5-768dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47502493 | |||||
| chr6:47502493
|
GT | G | 6 | a0001c0001t0002g0062a0001c0001t0002g0096a0001c0001t0003g0017others(3): Show | 6 | HG01943.hp1 HG02300.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.5-768delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 47502493 | |||||
| chr6:47502555
|
A | G | 307 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(304): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.5-725A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47502555 | ||||||
| chr6:47502557
|
G | A | 2 | a0001c0001t0077g0113a0001c0001t0088g0112 | 2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.5-723G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47502557 | ||||||
| chr6:47502603
|
C | T | 1 | a0001c0001t0003g0045 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.5-677C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47502603 | ||||||
| chr6:47502745
|
G | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.5-535G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47502745 | ||||||
| chr6:47502785
|
C | A | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.5-495C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47502785 | ||||||
| chr6:47503260
|
G | A | 4 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0071others(1): Show | 4 | NA18942.hp1 NA18946.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.5-20G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 1/17 | chr6 | 47503260 | ||||||
| chr6:47503604
|
G | A | 1 | a0001c0001t0062g0163 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.165+164G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47503604 | ||||||
| chr6:47503713
|
G | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.165+273G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47503713 | ||||||
| chr6:47503781
|
C | T | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165+341C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47503781 | ||||||
| chr6:47503789
|
T | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.165+349T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47503789 | ||||||
| chr6:47503922
|
C | T | 1 | a0001c0001t0073g0075 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.165+482C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47503922 | ||||||
| chr6:47503934
|
C | T | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.165+494C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47503934 | ||||||
| chr6:47503980
|
CT | C | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+545delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47503980 | |||||
| chr6:47504069
|
C | T | 1 | a0001c0001t0069g0100 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.165+629C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47504069 | ||||||
| chr6:47504420
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+980A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47504420 | ||||||
| chr6:47504563
|
C | T | 96 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.165+1123C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47504563 | ||||||
| chr6:47504635
|
C | T | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.165+1195C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47504635 | ||||||
| chr6:47504687
|
G | GAGA | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.165+1248_165+1250d others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47504687 | |||||
| chr6:47504869
|
A | G | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.165+1429A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47504869 | ||||||
| chr6:47504895
|
A | C | 1 | a0001c0001t0017g0044 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.165+1455A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47504895 | ||||||
| chr6:47505011
|
C | CT | 48 | a0001c0001t0002g0018a0001c0001t0002g0023a0001c0001t0002g0026others(45): Show | 48 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.165+1596dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505011 | |||||
| chr6:47505011
|
C | CTT | 70 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0019others(67): Show | 70 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.165+1595_165+1596d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505011 | |||||
| chr6:47505011
|
C | CTTT | 8 | a0001c0001t0002g0071a0001c0001t0002g0074a0001c0001t0002g0077others(5): Show | 8 | HG03486.hp2 HG03516.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+1594_165+1596d others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505011 | |||||
| chr6:47505011
|
CTT | C | 24 | a0001c0001t0015g0263a0001c0001t0016g0292a0001c0001t0016g0295others(21): Show | 24 | HG01069.hp2 HG01255.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.165+1595_165+1596d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505011 | |||||
| chr6:47505011
|
CTTT | C | 70 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0215others(67): Show | 70 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.165+1594_165+1596d others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505011 | |||||
| chr6:47505011
|
CTTTT | C | 8 | a0001c0001t0001g0213a0001c0001t0001g0226a0001c0001t0001g0232others(5): Show | 8 | HG00323.hp1 HG01256.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.165+1593_165+1596d others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505011 | |||||
| chr6:47505011
|
CTTTTTTT others(4): Show |
C | 61 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(58): Show | 61 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.165+1586_165+1596d others(13): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505011 | |||||
| chr6:47505011
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0010g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.165+1585_165+1596d others(14): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505011 | |||||
| chr6:47505011
|
CTTTTTTT others(7): Show |
C | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+1583_165+1596d others(16): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505011 | |||||
| chr6:47505022
|
T | C | 1 | a0001c0001t0011g0253 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.165+1582T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505022 | ||||||
| chr6:47505035
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.165+1595T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505035 | ||||||
| chr6:47505075
|
C | T | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.165+1635C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505075 | ||||||
| chr6:47505149
|
C | CTG | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.165+1709_165+1710i others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505149 | ||||||
| chr6:47505174
|
G | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.165+1734G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505174 | ||||||
| chr6:47505235
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.165+1795C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505235 | ||||||
| chr6:47505327
|
G | A | 3 | a0001c0001t0006g0167a0001c0001t0008g0310a0001c0001t0042g0168 | 3 | HG01891.hp2 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.165+1887G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505327 | ||||||
| chr6:47505471
|
C | T | 80 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.165+2031C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505471 | ||||||
| chr6:47505524
|
G | A | 1 | a0001c0001t0042g0192 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.165+2084G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505524 | ||||||
| chr6:47505538
|
G | A | 96 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.165+2098G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505538 | ||||||
| chr6:47505584
|
C | G | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.165+2144C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505584 | ||||||
| chr6:47505587
|
A | ACCTCCCG others(45): Show |
1 | a0001c0001t0020g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.165+2174_165+2225d others(54): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505587 | |||||
| chr6:47505587
|
ACCTCCCG others(45): Show |
A | 5 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0062others(2): Show | 5 | HG01109.hp1 HG01496.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+2174_165+2225d others(54): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505587 | |||||
| chr6:47505593
|
C | T | 1 | a0001c0001t0016g0295 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.165+2153C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505593 | ||||||
| chr6:47505614
|
C | T | 10 | a0001c0001t0003g0053a0001c0001t0009g0002a0001c0001t0013g0013others(7): Show | 10 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+2174C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505614 | ||||||
| chr6:47505616
|
G | GGGGGGCC others(670): Show |
69 | a0001c0001t0004g0105a0001c0001t0004g0114a0001c0001t0004g0123others(66): Show | 69 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.165+2181_165+2182i others(679): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505616 | |||||
| chr6:47505616
|
G | GGGGGGCC others(671): Show |
1 | a0001c0001t0014g0133 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.165+2181_165+2182i others(680): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505616 | |||||
| chr6:47505616
|
G | GGGGGGCC others(670): Show |
2 | a0001c0001t0039g0134a0001c0001t0039g0135 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.165+2181_165+2182i others(679): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505616 | |||||
| chr6:47505616
|
G | GGGGGGCC others(672): Show |
1 | a0001c0001t0010g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.165+2181_165+2182i others(681): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505616 | |||||
| chr6:47505616
|
G | GGGGGGCC others(671): Show |
1 | a0001c0001t0059g0298 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.165+2181_165+2182i others(680): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505616 | |||||
| chr6:47505616
|
G | GGGGGGCC others(670): Show |
2 | a0001c0001t0071g0205a0001c0001t0076g0206 | 2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.165+2181_165+2182i others(679): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505616 | |||||
| chr6:47505616
|
G | GGGGGGCC others(671): Show |
2 | a0001c0001t0004g0136a0001c0001t0079g0104 | 2 | HG02135.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.165+2181_165+2182i others(680): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505616 | |||||
| chr6:47505616
|
G | GGGGGGCC others(672): Show |
1 | a0001c0001t0004g0110 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.165+2181_165+2182i others(681): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505616 | |||||
| chr6:47505616
|
G | GGGGGGCC others(673): Show |
1 | a0001c0001t0007g0137 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.165+2181_165+2182i others(682): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505616 | |||||
| chr6:47505616
|
G | GGGGGGCC others(674): Show |
1 | a0001c0001t0010g0150 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.165+2181_165+2182i others(683): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505616 | |||||
| chr6:47505616
|
G | GGGGGGCC others(672): Show |
1 | a0001c0001t0084g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.165+2181_165+2182i others(681): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505616 | |||||
| chr6:47505616
|
G | GGGGGGCC others(671): Show |
1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165+2181_165+2182i others(680): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505616 | |||||
| chr6:47505621
|
G | GGCTGACC others(754): Show |
1 | a0001c0001t0001g0283 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.165+2225_165+2226i others(763): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505621 | |||||
| chr6:47505621
|
G | GGCTGACC others(754): Show |
1 | a0001c0001t0001g0249 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.165+2225_165+2226i others(763): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505621 | |||||
| chr6:47505621
|
G | GGCTGACC others(806): Show |
1 | a0001c0001t0011g0250 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.165+2194_165+2195i others(815): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505621 | |||||
| chr6:47505621
|
G | GGGCTGAC others(806): Show |
1 | a0001c0001t0011g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.165+2182_165+2183i others(815): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505621 | |||||
| chr6:47505621
|
G | GGGCTGAC others(809): Show |
1 | a0001c0001t0011g0259 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.165+2182_165+2183i others(818): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505621 | |||||
| chr6:47505626
|
AC | A | 82 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.165+2194delC | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505626 | |||||
| chr6:47505627
|
C | CCCCCCCA others(799): Show |
1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.165+2193_165+2194i others(808): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(800): Show |
9 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(6): Show | 9 | NA18943.hp1 NA18950.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+2225_165+2226i others(809): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(804): Show |
1 | a0001c0001t0001g0208 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.165+2225_165+2226i others(813): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(751): Show |
3 | a0001c0001t0001g0213a0001c0001t0001g0239a0001c0001t0045g0214 | 3 | HG00323.hp1 HG01515.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.165+2225_165+2226i others(760): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(800): Show |
1 | a0001c0001t0001g0232 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.165+2225_165+2226i others(809): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(800): Show |
39 | a0001c0001t0001g0215a0001c0001t0001g0223a0001c0001t0001g0226others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.165+2225_165+2226i others(809): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(849): Show |
3 | a0001c0001t0028g0210a0001c0001t0054g0211a0001c0001t0057g0288 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.165+2225_165+2226i others(858): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(802): Show |
1 | a0001c0001t0015g0263 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.165+2225_165+2226i others(811): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(801): Show |
1 | a0001c0001t0001g0275 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.165+2225_165+2226i others(810): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(802): Show |
1 | a0001c0001t0021g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.165+2225_165+2226i others(811): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(801): Show |
1 | a0001c0001t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.165+2225_165+2226i others(810): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(856): Show |
1 | a0001c0001t0028g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.165+2225_165+2226i others(865): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(850): Show |
1 | a0001c0001t0053g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.165+2225_165+2226i others(859): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(800): Show |
1 | a0005c0007t0005g0224 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.165+2225_165+2226i others(809): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(801): Show |
1 | a0001c0001t0051g0287 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.165+2225_165+2226i others(810): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(803): Show |
1 | a0001c0001t0001g0212 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.165+2225_165+2226i others(812): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(851): Show |
1 | a0001c0001t0055g0098 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.165+2225_165+2226i others(860): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(806): Show |
1 | a0001c0001t0011g0265 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.165+2225_165+2226i others(815): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(801): Show |
1 | a0001c0001t0001g0258 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.165+2225_165+2226i others(810): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(801): Show |
1 | a0001c0001t0001g0225 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.165+2194_165+2195i others(810): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(849): Show |
2 | a0003c0004t0032g0312a0003c0004t0061g0311 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+2194_165+2195i others(858): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505627
|
C | CCCCCCCC others(849): Show |
1 | a0006c0010t0032g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.165+2194_165+2195i others(858): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505627 | |||||
| chr6:47505645
|
C | T | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.165+2205C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505645 | ||||||
| chr6:47505654
|
C | T | 1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.165+2214C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505654 | ||||||
| chr6:47505662
|
C | CGGGCGGG others(800): Show |
3 | a0001c0001t0001g0233a0001c0001t0001g0247a0001c0001t0001g0257 | 3 | NA18939.hp1 NA18985.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.165+2225_165+2226i others(809): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505662 | |||||
| chr6:47505666
|
T | C | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2226T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505666 | ||||||
| chr6:47505667
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.165+2227G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505667 | ||||||
| chr6:47505667
|
G | GGGGGGCT others(623): Show |
2 | a0002c0002t0001g0278a0002c0002t0001g0279 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.165+2232_165+2233i others(632): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505667 | |||||
| chr6:47505667
|
G | GGGGGGCT others(623): Show |
2 | a0002c0002t0001g0276a0002c0002t0001g0280 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.165+2232_165+2233i others(632): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505667 | |||||
| chr6:47505673
|
G | A | 1 | a0001c0001t0004g0146 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.165+2233G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505673 | ||||||
| chr6:47505686
|
T | C | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2246T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505686 | ||||||
| chr6:47505699
|
C | T | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2259C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505699 | ||||||
| chr6:47505704
|
T | C | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2264T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505704 | ||||||
| chr6:47505717
|
T | A | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2277T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505717 | ||||||
| chr6:47505773
|
C | T | 2 | a0001c0001t0062g0163a0001c0001t0063g0164 | 2 | NA18977.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.165+2333C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505773 | ||||||
| chr6:47505774
|
G | A | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2334G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505774 | ||||||
| chr6:47505799
|
G | C | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2359G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505799 | ||||||
| chr6:47505802
|
T | G | 1 | a0001c0001t0001g0240 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.165+2362T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505802 | ||||||
| chr6:47505822
|
T | C | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2382T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505822 | ||||||
| chr6:47505827
|
G | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.165+2387G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505827 | ||||||
| chr6:47505829
|
C | G | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2389C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505829 | ||||||
| chr6:47505830
|
A | G | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2390A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505830 | ||||||
| chr6:47505837
|
T | G | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2397T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505837 | ||||||
| chr6:47505839
|
CG | C | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2402delG | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505839 | |||||
| chr6:47505843
|
C | T | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2403C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505843 | ||||||
| chr6:47505844
|
G | C | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2404G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505844 | ||||||
| chr6:47505844
|
G | GGGGGGGC others(120): Show |
4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2420_165+2421i others(129): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505844 | |||||
| chr6:47505888
|
C | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+2448C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505888 | ||||||
| chr6:47505902
|
A | AC | 243 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(240): Show | 243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.165+2470dupC | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505902 | |||||
| chr6:47505902
|
A | ACC | 21 | a0001c0001t0001g0240a0001c0001t0001g0254a0001c0001t0001g0266others(18): Show | 21 | HG00438.hp1 HG00597.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.165+2469_165+2470d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47505902 | |||||
| chr6:47505921
|
C | T | 1 | a0001c0001t0006g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.165+2481C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505921 | ||||||
| chr6:47505922
|
G | C | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+2482G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505922 | ||||||
| chr6:47505925
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.165+2485C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505925 | ||||||
| chr6:47505926
|
G | T | 1 | a0001c0001t0008g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.165+2486G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505926 | ||||||
| chr6:47505942
|
G | A | 1 | a0001c0001t0013g0059 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.165+2502G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505942 | ||||||
| chr6:47505947
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.165+2507C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47505947 | ||||||
| chr6:47506043
|
G | C | 2 | a0003c0004t0032g0312a0003c0004t0061g0311 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+2603G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506043 | ||||||
| chr6:47506086
|
G | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2646G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506086 | ||||||
| chr6:47506091
|
G | A | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165+2651G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506091 | ||||||
| chr6:47506144
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.165+2704C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506144 | ||||||
| chr6:47506168
|
G | A | 6 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0053g0097others(3): Show | 6 | HG01255.hp2 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+2728G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506168 | ||||||
| chr6:47506182
|
G | A | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.165+2742G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506182 | ||||||
| chr6:47506210
|
C | T | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.165+2770C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506210 | ||||||
| chr6:47506313
|
C | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+2873C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506313 | ||||||
| chr6:47506337
|
A | G | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.165+2897A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506337 | ||||||
| chr6:47506356
|
G | A | 95 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0019others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.165+2916G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506356 | ||||||
| chr6:47506362
|
C | T | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.165+2922C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506362 | ||||||
| chr6:47506394
|
C | CG | 12 | a0001c0001t0001g0208a0001c0001t0001g0258a0001c0001t0001g0268others(9): Show | 12 | HG00597.hp2 HG01069.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+2958dupG | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47506394 | |||||
| chr6:47506394
|
C | T | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165+2954C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506394 | ||||||
| chr6:47506426
|
G | C | 11 | a0001c0001t0004g0123a0001c0001t0004g0125a0001c0001t0007g0122others(8): Show | 11 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+2986G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506426 | ||||||
| chr6:47506450
|
C | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+3010C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506450 | ||||||
| chr6:47506451
|
G | A | 1 | a0001c0001t0009g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.165+3011G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506451 | ||||||
| chr6:47506478
|
C | T | 1 | a0001c0001t0004g0114 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.165+3038C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506478 | ||||||
| chr6:47506500
|
A | G | 1 | a0001c0001t0011g0250 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.165+3060A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506500 | ||||||
| chr6:47506534
|
C | T | 1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.165+3094C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506534 | ||||||
| chr6:47506557
|
C | T | 1 | a0001c0001t0021g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.165+3117C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506557 | ||||||
| chr6:47506566
|
G | A | 98 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(95): Show | 98 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.165+3126G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506566 | ||||||
| chr6:47506608
|
C | T | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165+3168C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506608 | ||||||
| chr6:47506616
|
A | G | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.165+3176A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506616 | ||||||
| chr6:47506683
|
C | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.165+3243C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506683 | ||||||
| chr6:47506690
|
G | C | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.165+3250G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506690 | ||||||
| chr6:47506728
|
C | T | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0275 | 3 | NA18941.hp1 NA18994.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.165+3288C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506728 | ||||||
| chr6:47506743
|
AC | A | 96 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.165+3304delC | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506743 | ||||||
| chr6:47506761
|
C | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+3321C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506761 | ||||||
| chr6:47506789
|
G | T | 1 | a0001c0001t0007g0101 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.165+3349G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506789 | ||||||
| chr6:47506793
|
CGGAGGG | C | 38 | a0001c0001t0001g0212a0001c0001t0001g0215a0001c0001t0001g0223others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.165+3354_165+3359d others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506793 | ||||||
| chr6:47506793
|
CGGAGGGA others(5): Show |
C | 32 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0225others(29): Show | 32 | HG00323.hp1 HG01109.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.165+3354_165+3365d others(14): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506793 | ||||||
| chr6:47506793
|
CGGAGGGA others(11): Show |
C | 3 | a0001c0001t0053g0097a0001c0001t0055g0098a0002c0002t0001g0276 | 3 | HG01243.hp1 HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.165+3354_165+3371d others(20): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506793 | ||||||
| chr6:47506793
|
CGGAGGGA others(17): Show |
C | 85 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.165+3354_165+3377d others(26): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506793 | ||||||
| chr6:47506793
|
CGGAGGGA others(23): Show |
C | 5 | a0001c0001t0007g0101a0001c0001t0028g0209a0001c0001t0028g0210others(2): Show | 5 | HG01074.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+3354_165+3383d others(32): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506793 | ||||||
| chr6:47506794
|
G | A | 5 | a0001c0001t0005g0219a0001c0001t0005g0220a0001c0001t0005g0221others(2): Show | 5 | NA18612.hp1 NA18975.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+3354G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506794 | ||||||
| chr6:47506794
|
GGAGGGA | G | 9 | a0001c0001t0012g0200a0001c0001t0012g0201a0001c0001t0012g0322others(6): Show | 9 | HG00741.hp1 HG02451.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+3406_165+3411d others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47506794 | |||||
| chr6:47506794
|
GGAGGGAG others(5): Show |
G | 43 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(40): Show | 43 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.165+3400_165+3411d others(14): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47506794 | |||||
| chr6:47506794
|
GGAGGGAG others(11): Show |
G | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.165+3394_165+3411d others(20): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47506794 | |||||
| chr6:47506794
|
GGAGGGAG others(17): Show |
G | 1 | a0001c0001t0025g0057 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.165+3388_165+3411d others(26): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47506794 | |||||
| chr6:47506794
|
GGAGGGAG others(23): Show |
G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.165+3382_165+3411d others(32): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47506794 | |||||
| chr6:47506796
|
AGGGAGAG others(12): Show |
A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.165+3359_165+3377d others(21): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47506796 | |||||
| chr6:47506858
|
T | C | 1 | a0001c0001t0067g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.165+3418T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506858 | ||||||
| chr6:47506899
|
A | T | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.165+3459A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506899 | ||||||
| chr6:47506979
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.165+3539A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506979 | ||||||
| chr6:47506994
|
G | A | 75 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.165+3554G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47506994 | ||||||
| chr6:47507124
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.165+3684C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47507124 | ||||||
| chr6:47507212
|
T | C | 96 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.165+3772T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47507212 | ||||||
| chr6:47507226
|
C | T | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.165+3786C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47507226 | ||||||
| chr6:47507286
|
T | G | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.165+3846T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47507286 | ||||||
| chr6:47507403
|
T | A | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.165+3963T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47507403 | ||||||
| chr6:47507474
|
G | A | 1 | a0001c0001t0021g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.165+4034G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47507474 | ||||||
| chr6:47507487
|
T | TG | 96 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.165+4051dupG | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47507487 | |||||
| chr6:47507542
|
C | T | 1 | a0001c0001t0073g0075 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.165+4102C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47507542 | ||||||
| chr6:47507603
|
G | A | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.165+4163G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47507603 | ||||||
| chr6:47508048
|
C | G | 1 | a0001c0001t0071g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.165+4608C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47508048 | ||||||
| chr6:47508118
|
T | C | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.165+4678T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47508118 | ||||||
| chr6:47508162
|
G | A | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.165+4722G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47508162 | ||||||
| chr6:47508170
|
T | C | 319 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.165+4730T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47508170 | ||||||
| chr6:47508534
|
CT | C | 146 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.165+5105delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47508534 | |||||
| chr6:47508534
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.165+5106_165+5117d others(14): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47508534 | |||||
| chr6:47508543
|
TTTG | T | 7 | a0001c0001t0007g0155a0001c0001t0071g0205a0001c0001t0076g0206others(4): Show | 7 | HG03225.hp2 HG03453.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+5106_165+5108d others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47508543 | |||||
| chr6:47508544
|
TTG | T | 83 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0071others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.165+5106_165+5107d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47508544 | |||||
| chr6:47508545
|
T | G | 31 | a0001c0001t0001g0225a0001c0001t0001g0234a0001c0001t0001g0249others(28): Show | 31 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.165+5105T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47508545 | ||||||
| chr6:47508546
|
G | GT | 7 | a0001c0001t0006g0167a0001c0001t0006g0316a0001c0001t0008g0310others(4): Show | 7 | HG00735.hp1 HG01169.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+5123dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47508546 | |||||
| chr6:47508546
|
G | T | 31 | a0001c0001t0001g0225a0001c0001t0001g0234a0001c0001t0001g0249others(28): Show | 31 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.165+5106G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47508546 | ||||||
| chr6:47508547
|
T | G | 83 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0071others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.165+5107T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47508547 | ||||||
| chr6:47508548
|
T | G | 7 | a0001c0001t0007g0155a0001c0001t0071g0205a0001c0001t0076g0206others(4): Show | 7 | HG03225.hp2 HG03453.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+5108T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47508548 | ||||||
| chr6:47508557
|
T | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.165+5117T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47508557 | ||||||
| chr6:47508569
|
G | A | 1 | a0001c0001t0003g0076 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.165+5129G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47508569 | ||||||
| chr6:47508577
|
G | A | 3 | a0001c0001t0012g0322a0001c0001t0048g0321a0001c0001t0065g0197 | 3 | HG02559.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.165+5137G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47508577 | ||||||
| chr6:47508604
|
A | G | 306 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.165+5164A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47508604 | ||||||
| chr6:47508646
|
A | G | 1 | a0001c0001t0001g0275 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.165+5206A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47508646 | ||||||
| chr6:47509039
|
A | G | 1 | a0001c0001t0002g0041 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.165+5599A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47509039 | ||||||
| chr6:47509210
|
T | G | 1 | a0001c0001t0001g0266 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.165+5770T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47509210 | ||||||
| chr6:47509321
|
T | TG | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+5882dupG | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47509321 | |||||
| chr6:47509376
|
C | A | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165+5936C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47509376 | ||||||
| chr6:47509398
|
G | T | 75 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.165+5958G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47509398 | ||||||
| chr6:47509410
|
C | T | 1 | a0001c0001t0006g0315 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.165+5970C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47509410 | ||||||
| chr6:47509437
|
T | TA | 163 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.165+6012dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47509437 | |||||
| chr6:47509474
|
G | A | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.165+6034G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47509474 | ||||||
| chr6:47509603
|
G | T | 1 | a0001c0001t0005g0260 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.165+6163G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47509603 | ||||||
| chr6:47509671
|
T | C | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.165+6231T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47509671 | ||||||
| chr6:47509921
|
A | G | 306 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.165+6481A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47509921 | ||||||
| chr6:47510058
|
C | A | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.165+6618C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47510058 | ||||||
| chr6:47510062
|
C | T | 1 | a0001c0008t0001g0244 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.165+6622C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47510062 | ||||||
| chr6:47510128
|
A | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.165+6688A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47510128 | ||||||
| chr6:47510197
|
C | T | 85 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.165+6757C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47510197 | ||||||
| chr6:47510477
|
A | G | 1 | a0001c0001t0006g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.165+7037A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47510477 | ||||||
| chr6:47510514
|
G | A | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.165+7074G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47510514 | ||||||
| chr6:47510577
|
A | G | 1 | a0001c0001t0003g0078 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.165+7137A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47510577 | ||||||
| chr6:47510664
|
C | T | 1 | a0001c0001t0002g0041 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.165+7224C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47510664 | ||||||
| chr6:47510719
|
T | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+7279T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47510719 | ||||||
| chr6:47510998
|
G | C | 1 | a0001c0001t0071g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.165+7558G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47510998 | ||||||
| chr6:47511027
|
C | T | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.165+7587C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47511027 | ||||||
| chr6:47511045
|
CCTGGTGA others(3): Show |
C | 1 | a0001c0001t0089g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.165+7606_165+7615d others(12): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47511045 | ||||||
| chr6:47511073
|
C | CA | 87 | a0001c0001t0003g0045a0001c0001t0004g0110a0001c0001t0004g0114others(84): Show | 87 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.165+7660dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47511073 | |||||
| chr6:47511073
|
C | CAA | 13 | a0001c0001t0004g0105a0001c0001t0004g0123a0001c0001t0007g0137others(10): Show | 13 | HG01192.hp1 HG01978.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+7659_165+7660d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47511073 | |||||
| chr6:47511073
|
CA | C | 19 | a0001c0001t0001g0215a0001c0001t0001g0247a0001c0001t0001g0249others(16): Show | 19 | HG00099.hp2 HG01069.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.165+7660delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47511073 | |||||
| chr6:47511073
|
CAA | C | 61 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.165+7659_165+7660d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47511073 | |||||
| chr6:47511102
|
G | T | 1 | a0001c0001t0067g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.165+7662G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47511102 | ||||||
| chr6:47511122
|
ATAGTAGC others(1): Show |
A | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.165+7692_165+7699d others(10): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47511122 | |||||
| chr6:47511156
|
G | A | 4 | a0001c0001t0035g0103a0001c0001t0076g0206a0001c0001t0079g0104others(1): Show | 4 | HG02451.hp2 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+7716G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47511156 | ||||||
| chr6:47511400
|
G | A | 61 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(58): Show | 61 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.165+7960G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47511400 | ||||||
| chr6:47511882
|
C | T | 82 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.165+8442C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47511882 | ||||||
| chr6:47511886
|
G | GGGT | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.165+8449_165+8451d others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47511886 | |||||
| chr6:47511921
|
G | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+8481G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47511921 | ||||||
| chr6:47512090
|
G | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+8650G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512090 | ||||||
| chr6:47512103
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.165+8663A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512103 | ||||||
| chr6:47512144
|
C | G | 1 | a0001c0001t0071g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.165+8704C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512144 | ||||||
| chr6:47512152
|
C | T | 1 | a0001c0001t0095g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.165+8712C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512152 | ||||||
| chr6:47512166
|
A | T | 12 | a0001c0001t0001g0273a0001c0001t0003g0045a0001c0001t0013g0058others(9): Show | 12 | HG02818.hp2 HG02886.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.165+8726A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512166 | ||||||
| chr6:47512168
|
T | A | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.165+8728T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512168 | ||||||
| chr6:47512297
|
G | A | 1 | a0001c0001t0098g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.165+8857G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512297 | ||||||
| chr6:47512330
|
A | C | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+8890A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512330 | ||||||
| chr6:47512354
|
C | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+8914C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512354 | ||||||
| chr6:47512363
|
G | C | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+8923G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512363 | ||||||
| chr6:47512377
|
G | T | 1 | a0001c0001t0001g0223 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.165+8937G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512377 | ||||||
| chr6:47512577
|
T | G | 1 | a0002c0002t0001g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.165+9137T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512577 | ||||||
| chr6:47512640
|
A | C | 3 | a0001c0001t0036g0158a0001c0001t0036g0159a0001c0001t0084g0160 | 3 | HG02055.hp2 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.165+9200A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512640 | ||||||
| chr6:47512789
|
C | T | 1 | a0001c0001t0012g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.165+9349C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512789 | ||||||
| chr6:47512940
|
A | G | 62 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.165+9500A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47512940 | ||||||
| chr6:47513143
|
CT | C | 211 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.165+9719delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47513143 | |||||
| chr6:47513143
|
CTT | C | 6 | a0001c0001t0015g0261a0001c0001t0030g0302a0001c0001t0062g0163others(3): Show | 6 | HG02486.hp1 HG02723.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+9718_165+9719d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47513143 | |||||
| chr6:47513157
|
T | C | 7 | a0001c0001t0006g0180a0001c0001t0006g0183a0001c0001t0008g0178others(4): Show | 7 | HG01255.hp2 HG01358.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+9717T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47513157 | ||||||
| chr6:47513239
|
C | G | 82 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.165+9799C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47513239 | ||||||
| chr6:47513292
|
T | C | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+9852T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47513292 | ||||||
| chr6:47513552
|
CT | C | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+10113delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47513552 | ||||||
| chr6:47513632
|
A | G | 1 | a0001c0001t0007g0101 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.165+10192A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47513632 | ||||||
| chr6:47513648
|
C | T | 1 | a0001c0001t0004g0146 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.165+10208C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47513648 | ||||||
| chr6:47513778
|
C | T | 1 | a0001c0001t0002g0040 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.165+10338C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47513778 | ||||||
| chr6:47513875
|
T | A | 2 | a0001c0001t0041g0189a0001c0001t0080g0207 | 2 | HG01261.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.165+10435T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47513875 | ||||||
| chr6:47513875
|
T | TA | 63 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.165+10443dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47513875 | |||||
| chr6:47513884
|
T | A | 19 | a0001c0001t0004g0123a0001c0001t0004g0125a0001c0001t0007g0101others(16): Show | 19 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.165+10444T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47513884 | ||||||
| chr6:47513892
|
T | G | 63 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.165+10452T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47513892 | ||||||
| chr6:47513893
|
G | T | 1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.165+10453G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47513893 | ||||||
| chr6:47513895
|
G | C | 1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.165+10455G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47513895 | ||||||
| chr6:47514097
|
C | G | 62 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.165+10657C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514097 | ||||||
| chr6:47514128
|
G | A | 1 | a0001c0001t0078g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.165+10688G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514128 | ||||||
| chr6:47514218
|
T | C | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+10778T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514218 | ||||||
| chr6:47514277
|
C | T | 307 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(304): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.165+10837C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514277 | ||||||
| chr6:47514337
|
T | A | 96 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.165+10897T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514337 | ||||||
| chr6:47514343
|
A | T | 11 | a0001c0001t0004g0123a0001c0001t0004g0125a0001c0001t0007g0122others(8): Show | 11 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+10903A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514343 | ||||||
| chr6:47514375
|
A | G | 1 | a0001c0001t0100g0187 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.165+10935A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514375 | ||||||
| chr6:47514416
|
A | C | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+10976A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514416 | ||||||
| chr6:47514418
|
G | A | 77 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.165+10978G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514418 | ||||||
| chr6:47514458
|
A | G | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.165+11018A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514458 | ||||||
| chr6:47514538
|
TAAAAC | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+11103_165+1110 others(9): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47514538 | |||||
| chr6:47514583
|
G | A | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.165+11143G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514583 | ||||||
| chr6:47514720
|
C | T | 1 | a0001c0001t0038g0051 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.165+11280C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514720 | ||||||
| chr6:47514745
|
A | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.165+11305A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514745 | ||||||
| chr6:47514883
|
C | G | 1 | a0001c0001t0081g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.165+11443C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514883 | ||||||
| chr6:47514922
|
C | T | 1 | a0001c0001t0071g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.165+11482C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514922 | ||||||
| chr6:47514926
|
C | T | 1 | a0001c0001t0052g0301 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.165+11486C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47514926 | ||||||
| chr6:47515047
|
G | A | 73 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.165+11607G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47515047 | ||||||
| chr6:47515051
|
TA | T | 7 | a0001c0001t0001g0232a0001c0001t0001g0234a0001c0001t0002g0073others(4): Show | 7 | HG01516.hp2 HG01975.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+11627delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47515051 | |||||
| chr6:47515151
|
T | C | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.165+11711T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47515151 | ||||||
| chr6:47515163
|
A | G | 96 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.165+11723A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47515163 | ||||||
| chr6:47515271
|
G | A | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.165+11831G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47515271 | ||||||
| chr6:47515440
|
C | T | 2 | a0001c0001t0019g0039a0001c0001t0019g0084 | 2 | NA19000.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.165+12000C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47515440 | ||||||
| chr6:47515815
|
A | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.165+12375A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47515815 | ||||||
| chr6:47515917
|
C | G | 62 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.165+12477C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47515917 | ||||||
| chr6:47515963
|
G | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+12523G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47515963 | ||||||
| chr6:47516315
|
G | C | 168 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.165+12875G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47516315 | ||||||
| chr6:47516353
|
T | A | 1 | a0001c0001t0071g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.165+12913T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47516353 | ||||||
| chr6:47516714
|
G | C | 5 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0062others(2): Show | 5 | HG01109.hp1 HG01496.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+13274G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47516714 | ||||||
| chr6:47516729
|
G | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+13289G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47516729 | ||||||
| chr6:47516824
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.165+13384G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47516824 | ||||||
| chr6:47517003
|
G | A | 3 | a0001c0001t0006g0316a0001c0001t0006g0317a0001c0001t0006g0318 | 3 | NA18946.hp2 NA18966.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.165+13563G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47517003 | ||||||
| chr6:47517056
|
C | T | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.165+13616C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47517056 | ||||||
| chr6:47517108
|
C | T | 306 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.165+13668C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47517108 | ||||||
| chr6:47517175
|
G | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.165+13735G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47517175 | ||||||
| chr6:47517183
|
T | TTCTTCTT others(4): Show |
1 | a0001c0001t0014g0151 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.165+13744_165+1375 others(15): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47517183 | |||||
| chr6:47517266
|
T | C | 80 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.165+13826T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47517266 | ||||||
| chr6:47517284
|
CT | C | 11 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0275others(8): Show | 11 | HG01256.hp2 HG01975.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.165+13859delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47517284 | |||||
| chr6:47517285
|
T | C | 5 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0002g0023others(2): Show | 5 | NA18950.hp1 NA18967.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+13845T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47517285 | ||||||
| chr6:47517306
|
G | A | 1 | a0001c0001t0067g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.165+13866G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47517306 | ||||||
| chr6:47517362
|
G | A | 169 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.165+13922G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47517362 | ||||||
| chr6:47517386
|
C | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.165+13946C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47517386 | ||||||
| chr6:47517390
|
C | T | 63 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.165+13950C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47517390 | ||||||
| chr6:47517579
|
C | T | 1 | a0001c0001t0022g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.165+14139C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47517579 | ||||||
| chr6:47517598
|
CTT | C | 3 | a0001c0001t0037g0116a0001c0001t0037g0128a0001c0001t0093g0117 | 3 | HG02647.hp1 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.165+14162_165+1416 others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47517598 | |||||
| chr6:47517728
|
G | C | 1 | a0001c0001t0050g0218 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.165+14288G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47517728 | ||||||
| chr6:47517988
|
A | T | 1 | a0001c0008t0001g0244 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.165+14548A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47517988 | ||||||
| chr6:47518027
|
T | C | 1 | a0001c0001t0017g0044 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.165+14587T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47518027 | ||||||
| chr6:47518406
|
A | T | 1 | a0001c0001t0022g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165+14966A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47518406 | ||||||
| chr6:47518791
|
C | A | 3 | a0001c0001t0006g0180a0001c0001t0008g0178a0001c0001t0008g0182 | 3 | HG02056.hp1 NA18939.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.166-14811C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47518791 | ||||||
| chr6:47519222
|
A | G | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.166-14380A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47519222 | ||||||
| chr6:47519333
|
A | T | 321 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.166-14269A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47519333 | ||||||
| chr6:47519361
|
TGTGATG | T | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.166-14238_166-1423 others(10): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47519361 | |||||
| chr6:47519764
|
A | C | 1 | a0001c0001t0004g0132 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.166-13838A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47519764 | ||||||
| chr6:47520026
|
A | G | 63 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.166-13576A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47520026 | ||||||
| chr6:47520091
|
A | AT | 7 | a0001c0001t0001g0234a0001c0001t0001g0269a0001c0001t0002g0046others(4): Show | 7 | HG00438.hp1 HG01978.hp2 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-13499dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47520091 | |||||
| chr6:47520101
|
T | G | 1 | a0001c0001t0005g0241 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.166-13501T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47520101 | ||||||
| chr6:47520220
|
G | A | 1 | a0001c0001t0002g0040 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.166-13382G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47520220 | ||||||
| chr6:47520279
|
T | C | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.166-13323T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47520279 | ||||||
| chr6:47520299
|
T | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.166-13303T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47520299 | ||||||
| chr6:47520563
|
C | T | 1 | a0001c0001t0081g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.166-13039C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47520563 | ||||||
| chr6:47520568
|
G | A | 11 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0023others(8): Show | 11 | HG00733.hp2 HG00741.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-13034G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47520568 | ||||||
| chr6:47520609
|
G | A | 1 | a0001c0001t0071g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.166-12993G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47520609 | ||||||
| chr6:47520632
|
C | A | 1 | a0001c0001t0031g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-12970C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47520632 | ||||||
| chr6:47520651
|
G | A | 162 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.166-12951G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47520651 | ||||||
| chr6:47520692
|
A | C | 1 | a0001c0001t0005g0220 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.166-12910A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47520692 | ||||||
| chr6:47520697
|
G | A | 24 | a0001c0001t0006g0179a0001c0001t0006g0180a0001c0001t0006g0183others(21): Show | 24 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.166-12905G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47520697 | ||||||
| chr6:47520730
|
G | GT | 19 | a0001c0001t0002g0008a0001c0001t0002g0071a0001c0001t0002g0092others(16): Show | 19 | HG00423.hp2 HG00642.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.166-12850dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47520730 | |||||
| chr6:47520730
|
GT | G | 163 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.166-12850delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47520730 | |||||
| chr6:47521012
|
G | A | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.166-12590G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47521012 | ||||||
| chr6:47521202
|
G | A | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.166-12400G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47521202 | ||||||
| chr6:47521339
|
G | A | 39 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(36): Show | 39 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.166-12263G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47521339 | ||||||
| chr6:47521368
|
A | G | 63 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.166-12234A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47521368 | ||||||
| chr6:47521471
|
G | T | 1 | a0001c0001t0002g0038 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.166-12131G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47521471 | ||||||
| chr6:47521506
|
C | T | 1 | a0001c0001t0020g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.166-12096C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47521506 | ||||||
| chr6:47521507
|
G | C | 2 | a0001c0001t0002g0038a0001c0001t0002g0060 | 2 | HG01346.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.166-12095G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47521507 | ||||||
| chr6:47521678
|
A | T | 1 | a0001c0001t0100g0187 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.166-11924A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47521678 | ||||||
| chr6:47521832
|
G | A | 306 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.166-11770G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47521832 | ||||||
| chr6:47521942
|
G | T | 1 | a0001c0001t0001g0274 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.166-11660G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47521942 | ||||||
| chr6:47521972
|
G | A | 63 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.166-11630G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47521972 | ||||||
| chr6:47521996
|
C | G | 39 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(36): Show | 39 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.166-11606C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47521996 | ||||||
| chr6:47522002
|
C | T | 2 | a0001c0001t0021g0229a0001c0001t0021g0230 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.166-11600C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47522002 | ||||||
| chr6:47522003
|
G | A | 2 | a0001c0001t0006g0314a0001c0001t0011g0259 | 2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.166-11599G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47522003 | ||||||
| chr6:47522015
|
C | CA | 86 | a0001c0001t0001g0239a0001c0001t0002g0088a0001c0001t0004g0105others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.166-11576dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47522015 | |||||
| chr6:47522114
|
A | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.166-11488A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47522114 | ||||||
| chr6:47522130
|
C | T | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.166-11472C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47522130 | ||||||
| chr6:47522258
|
T | C | 3 | a0001c0001t0037g0116a0001c0001t0037g0128a0001c0001t0093g0117 | 3 | HG02647.hp1 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.166-11344T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47522258 | ||||||
| chr6:47522457
|
A | G | 83 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.166-11145A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47522457 | ||||||
| chr6:47522717
|
T | C | 1 | a0001c0001t0042g0192 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.166-10885T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47522717 | ||||||
| chr6:47522724
|
C | T | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.166-10878C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47522724 | ||||||
| chr6:47522801
|
G | A | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.166-10801G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47522801 | ||||||
| chr6:47522840
|
A | T | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.166-10762A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47522840 | ||||||
| chr6:47523026
|
A | G | 1 | a0001c0001t0007g0101 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.166-10576A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47523026 | ||||||
| chr6:47523047
|
A | G | 39 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(36): Show | 39 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.166-10555A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47523047 | ||||||
| chr6:47523288
|
G | C | 1 | a0001c0001t0004g0129 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.166-10314G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47523288 | ||||||
| chr6:47523402
|
T | G | 1 | a0001c0001t0075g0010 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.166-10200T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47523402 | ||||||
| chr6:47523496
|
C | A | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.166-10106C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47523496 | ||||||
| chr6:47523523
|
G | A | 1 | a0001c0001t0010g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.166-10079G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47523523 | ||||||
| chr6:47524005
|
A | G | 1 | a0001c0001t0046g0118 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.166-9597A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524005 | ||||||
| chr6:47524125
|
T | C | 1 | a0001c0001t0006g0314 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.166-9477T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524125 | ||||||
| chr6:47524167
|
G | A | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.166-9435G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524167 | ||||||
| chr6:47524280
|
T | C | 1 | a0001c0001t0002g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.166-9322T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524280 | ||||||
| chr6:47524301
|
C | T | 79 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(76): Show | 79 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.166-9301C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524301 | ||||||
| chr6:47524386
|
C | G | 169 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.166-9216C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524386 | ||||||
| chr6:47524423
|
G | A | 1 | a0001c0001t0035g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.166-9179G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524423 | ||||||
| chr6:47524610
|
G | GT | 92 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(89): Show | 92 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.166-8983dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47524610 | |||||
| chr6:47524618
|
T | TC | 77 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.166-8984_166-8983i others(3): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524618 | ||||||
| chr6:47524654
|
T | C | 1 | a0001c0001t0002g0032 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.166-8948T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524654 | ||||||
| chr6:47524850
|
G | T | 169 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.166-8752G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524850 | ||||||
| chr6:47524851
|
T | C | 169 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.166-8751T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524851 | ||||||
| chr6:47524895
|
A | G | 2 | a0001c0001t0021g0229a0001c0001t0021g0230 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.166-8707A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524895 | ||||||
| chr6:47524914
|
G | A | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.166-8688G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524914 | ||||||
| chr6:47524970
|
A | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.166-8632A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47524970 | ||||||
| chr6:47525177
|
A | T | 1 | a0001c0001t0031g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-8425A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47525177 | ||||||
| chr6:47525237
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.166-8365A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47525237 | ||||||
| chr6:47525582
|
A | G | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.166-8020A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47525582 | ||||||
| chr6:47525594
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.166-8008G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47525594 | ||||||
| chr6:47525649
|
A | G | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.166-7953A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47525649 | ||||||
| chr6:47525710
|
A | G | 169 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.166-7892A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47525710 | ||||||
| chr6:47525810
|
T | C | 83 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.166-7792T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47525810 | ||||||
| chr6:47525934
|
A | G | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.166-7668A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47525934 | ||||||
| chr6:47526052
|
C | T | 1 | a0001c0001t0096g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.166-7550C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47526052 | ||||||
| chr6:47526065
|
C | T | 1 | a0001c0001t0028g0210 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.166-7537C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47526065 | ||||||
| chr6:47526074
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.166-7528A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47526074 | ||||||
| chr6:47526204
|
G | A | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.166-7398G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47526204 | ||||||
| chr6:47526269
|
A | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.166-7333A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47526269 | ||||||
| chr6:47526510
|
G | A | 2 | a0001c0001t0002g0028a0001c0001t0002g0029 | 2 | NA18981.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.166-7092G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47526510 | ||||||
| chr6:47526982
|
A | C | 97 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(94): Show | 97 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.166-6620A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47526982 | ||||||
| chr6:47526995
|
T | C | 2 | a0001c0001t0012g0322a0001c0001t0048g0321 | 2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.166-6607T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47526995 | ||||||
| chr6:47527023
|
A | G | 82 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.166-6579A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527023 | ||||||
| chr6:47527031
|
G | A | 12 | a0001c0001t0004g0114a0001c0001t0004g0129a0001c0001t0004g0132others(9): Show | 12 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-6571G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527031 | ||||||
| chr6:47527106
|
T | TC | 150 | a0001c0001t0001g0285a0001c0001t0002g0006a0001c0001t0002g0008others(147): Show | 150 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.166-6489dupC | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47527106 | |||||
| chr6:47527113
|
C | CCCT | 70 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(67): Show | 70 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.166-6489_166-6488i others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527113 | ||||||
| chr6:47527146
|
A | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.166-6456A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527146 | ||||||
| chr6:47527181
|
A | G | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-6421A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527181 | ||||||
| chr6:47527311
|
T | C | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.166-6291T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527311 | ||||||
| chr6:47527398
|
A | G | 74 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.166-6204A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527398 | ||||||
| chr6:47527448
|
G | T | 2 | a0001c0001t0071g0205a0001c0001t0076g0206 | 2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.166-6154G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527448 | ||||||
| chr6:47527532
|
A | G | 1 | a0001c0001t0006g0315 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.166-6070A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527532 | ||||||
| chr6:47527687
|
G | C | 1 | a0001c0001t0012g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.166-5915G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527687 | ||||||
| chr6:47527713
|
C | T | 1 | a0001c0001t0063g0164 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.166-5889C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527713 | ||||||
| chr6:47527722
|
A | T | 2 | a0001c0001t0019g0039a0001c0001t0019g0084 | 2 | NA19000.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.166-5880A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527722 | ||||||
| chr6:47527758
|
A | T | 1 | a0001c0001t0081g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.166-5844A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527758 | ||||||
| chr6:47527988
|
T | G | 169 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.166-5614T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47527988 | ||||||
| chr6:47528381
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.166-5221G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47528381 | ||||||
| chr6:47528542
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.166-5060A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47528542 | ||||||
| chr6:47528999
|
G | T | 1 | a0001c0001t0008g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.166-4603G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47528999 | ||||||
| chr6:47529058
|
A | G | 1 | a0001c0001t0017g0044 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.166-4544A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47529058 | ||||||
| chr6:47529183
|
GC | G | 37 | a0001c0001t0002g0008a0001c0001t0002g0021a0001c0001t0002g0027others(34): Show | 37 | HG00140.hp1 HG00597.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.166-4402delC | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47529183 | |||||
| chr6:47529183
|
GCC | G | 77 | a0001c0001t0001g0285a0001c0001t0002g0006a0001c0001t0002g0018others(74): Show | 77 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.166-4403_166-4402d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47529183 | |||||
| chr6:47529183
|
GCCC | G | 86 | a0001c0001t0002g0038a0001c0001t0002g0086a0001c0001t0003g0089others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.166-4404_166-4402d others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47529183 | |||||
| chr6:47529183
|
GCCCC | G | 25 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0252others(22): Show | 25 | HG00558.hp1 HG00642.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.166-4405_166-4402d others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47529183 | |||||
| chr6:47529183
|
GCCCCC | G | 68 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0223others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.166-4406_166-4402d others(7): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47529183 | |||||
| chr6:47529196
|
C | A | 1 | a0001c0001t0002g0023 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.166-4406C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47529196 | ||||||
| chr6:47529275
|
G | A | 2 | a0001c0001t0075g0010a0001c0001t0078g0011 | 2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.166-4327G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47529275 | ||||||
| chr6:47529501
|
T | C | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.166-4101T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47529501 | ||||||
| chr6:47529524
|
C | T | 1 | a0001c0001t0021g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.166-4078C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47529524 | ||||||
| chr6:47529855
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.166-3747G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47529855 | ||||||
| chr6:47530024
|
C | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-3578C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47530024 | ||||||
| chr6:47530091
|
A | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.166-3511A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47530091 | ||||||
| chr6:47530195
|
T | A | 1 | a0001c0001t0014g0151 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.166-3407T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47530195 | ||||||
| chr6:47530309
|
A | G | 306 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.166-3293A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47530309 | ||||||
| chr6:47530415
|
T | A | 1 | a0001c0001t0003g0045 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.166-3187T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47530415 | ||||||
| chr6:47530475
|
C | G | 1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.166-3127C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47530475 | ||||||
| chr6:47530475
|
C | T | 1 | a0001c0001t0004g0132 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.166-3127C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47530475 | ||||||
| chr6:47530503
|
A | G | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.166-3099A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47530503 | ||||||
| chr6:47530551
|
G | A | 264 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(261): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.166-3051G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47530551 | ||||||
| chr6:47530611
|
T | C | 1 | a0001c0001t0071g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.166-2991T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47530611 | ||||||
| chr6:47530665
|
A | G | 4 | a0001c0001t0023g0198a0001c0001t0023g0202a0001c0001t0023g0203others(1): Show | 4 | HG00741.hp1 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-2937A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47530665 | ||||||
| chr6:47530897
|
A | C | 1 | a0001c0001t0089g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.166-2705A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47530897 | ||||||
| chr6:47530955
|
C | T | 1 | a0001c0001t0008g0310 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.166-2647C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47530955 | ||||||
| chr6:47531191
|
C | T | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.166-2411C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47531191 | ||||||
| chr6:47531323
|
A | G | 1 | a0001c0001t0042g0192 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.166-2279A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47531323 | ||||||
| chr6:47531392
|
T | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.166-2210T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47531392 | ||||||
| chr6:47531457
|
C | T | 1 | a0001c0001t0009g0020 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.166-2145C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47531457 | ||||||
| chr6:47531673
|
T | C | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.166-1929T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47531673 | ||||||
| chr6:47531725
|
G | T | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.166-1877G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47531725 | ||||||
| chr6:47531779
|
A | G | 1 | a0001c0001t0013g0047 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.166-1823A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47531779 | ||||||
| chr6:47531834
|
A | T | 1 | a0001c0001t0019g0061 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.166-1768A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47531834 | ||||||
| chr6:47531838
|
C | T | 1 | a0006c0010t0032g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.166-1764C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47531838 | ||||||
| chr6:47531848
|
A | G | 266 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(263): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.166-1754A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47531848 | ||||||
| chr6:47531873
|
G | C | 1 | a0001c0001t0003g0012 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.166-1729G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47531873 | ||||||
| chr6:47531902
|
G | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0248a0001c0001t0001g0252 | 3 | HG00639.hp2 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.166-1700G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47531902 | ||||||
| chr6:47532004
|
C | T | 2 | a0001c0001t0004g0105a0001c0001t0010g0106 | 2 | NA18949.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.166-1598C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47532004 | ||||||
| chr6:47532073
|
C | CA | 81 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(78): Show | 81 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.166-1518dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47532073 | |||||
| chr6:47532080
|
A | G | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.166-1522A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47532080 | ||||||
| chr6:47532139
|
A | G | 1 | a0006c0010t0032g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.166-1463A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47532139 | ||||||
| chr6:47532302
|
C | T | 1 | a0001c0001t0002g0086 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.166-1300C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47532302 | ||||||
| chr6:47532345
|
GA | G | 6 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(3): Show | 6 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-1244delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47532345 | |||||
| chr6:47532376
|
T | TAC | 4 | a0001c0001t0012g0322a0001c0001t0048g0321a0001c0001t0062g0163others(1): Show | 4 | HG02559.hp1 HG02818.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-1182_166-1181d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47532376 | |||||
| chr6:47532376
|
TAC | T | 6 | a0001c0001t0006g0180a0001c0001t0023g0198a0001c0001t0023g0202others(3): Show | 6 | HG00741.hp1 HG01884.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-1182_166-1181d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47532376 | |||||
| chr6:47532376
|
TACAC | T | 24 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0183others(21): Show | 24 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.166-1184_166-1181d others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47532376 | |||||
| chr6:47532376
|
TACACAC | T | 9 | a0001c0001t0006g0314a0001c0001t0006g0315a0001c0001t0006g0316others(6): Show | 9 | HG00099.hp1 HG02523.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-1186_166-1181d others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47532376 | |||||
| chr6:47532376
|
TACACACA others(1): Show |
T | 14 | a0001c0001t0003g0053a0001c0001t0013g0013a0001c0001t0013g0047others(11): Show | 14 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-1188_166-1181d others(10): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47532376 | |||||
| chr6:47532376
|
TACACACA others(3): Show |
T | 8 | a0001c0001t0002g0077a0001c0001t0009g0002a0001c0001t0013g0095others(5): Show | 8 | HG00140.hp1 HG01168.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-1190_166-1181d others(12): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47532376 | |||||
| chr6:47532376
|
TACACACA others(5): Show |
T | 79 | a0001c0001t0001g0240a0001c0001t0002g0006a0001c0001t0002g0008others(76): Show | 79 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.166-1192_166-1181d others(14): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47532376 | |||||
| chr6:47532376
|
TACACACA others(7): Show |
T | 131 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(128): Show | 131 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.166-1194_166-1181d others(16): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47532376 | |||||
| chr6:47532376
|
TACACACA others(9): Show |
T | 28 | a0001c0001t0001g0215a0001c0001t0004g0125a0001c0001t0016g0291others(25): Show | 28 | HG00099.hp2 HG00423.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.166-1196_166-1181d others(18): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47532376 | |||||
| chr6:47532376
|
TACACACA others(11): Show |
T | 1 | a0001c0001t0030g0304 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.166-1198_166-1181d others(20): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47532376 | |||||
| chr6:47532376
|
TACACACA others(13): Show |
T | 5 | a0001c0001t0041g0189a0001c0001t0043g0184a0001c0001t0043g0185others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-1200_166-1181d others(22): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 47532376 | |||||
| chr6:47532420
|
C | T | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.166-1182C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47532420 | ||||||
| chr6:47532813
|
A | G | 1 | a0001c0001t0016g0291 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.166-789A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47532813 | ||||||
| chr6:47532816
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.166-786A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47532816 | ||||||
| chr6:47532963
|
G | A | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.166-639G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47532963 | ||||||
| chr6:47532977
|
G | T | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.166-625G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47532977 | ||||||
| chr6:47533203
|
G | A | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.166-399G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47533203 | ||||||
| chr6:47533258
|
C | T | 91 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(88): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.166-344C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47533258 | ||||||
| chr6:47533260
|
A | G | 1 | a0001c0001t0010g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.166-342A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47533260 | ||||||
| chr6:47533268
|
C | G | 1 | a0001c0001t0003g0045 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.166-334C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47533268 | ||||||
| chr6:47533379
|
C | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.166-223C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47533379 | ||||||
| chr6:47533426
|
T | C | 1 | a0001c0001t0002g0032 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.166-176T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47533426 | ||||||
| chr6:47533559
|
A | C | 1 | a0001c0001t0024g0142 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.166-43A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 2/17 | chr6 | 47533559 | ||||||
| chr6:47533768
|
T | C | 1 | a0001c0001t0018g0025 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.319+13T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47533768 | ||||||
| chr6:47533834
|
T | C | 2 | a0001c0001t0010g0144a0001c0001t0024g0115 | 2 | HG01257.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.319+79T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47533834 | ||||||
| chr6:47533911
|
A | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.319+156A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47533911 | ||||||
| chr6:47534092
|
T | C | 2 | a0001c0001t0039g0134a0001c0001t0039g0135 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.319+337T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534092 | ||||||
| chr6:47534288
|
G | C | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.319+533G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534288 | ||||||
| chr6:47534301
|
G | C | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.319+546G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534301 | ||||||
| chr6:47534359
|
A | C | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.319+604A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534359 | ||||||
| chr6:47534375
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.319+620A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534375 | ||||||
| chr6:47534548
|
T | C | 1 | a0001c0001t0019g0061 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.319+793T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534548 | ||||||
| chr6:47534562
|
G | A | 2 | a0001c0001t0038g0051a0001c0005t0068g0001 | 2 | HG01433.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.319+807G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534562 | ||||||
| chr6:47534589
|
C | T | 1 | a0001c0001t0089g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.319+834C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534589 | ||||||
| chr6:47534628
|
T | A | 1 | a0001c0001t0017g0042 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.319+873T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534628 | ||||||
| chr6:47534687
|
A | G | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.319+932A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534687 | ||||||
| chr6:47534719
|
G | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.319+964G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534719 | ||||||
| chr6:47534735
|
G | A | 1 | a0001c0001t0100g0187 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.319+980G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534735 | ||||||
| chr6:47534803
|
C | CT | 91 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(88): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.319+1062dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 47534803 | |||||
| chr6:47534874
|
G | A | 2 | a0001c0001t0001g0243a0001c0001t0067g0196 | 2 | HG01074.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.319+1119G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534874 | ||||||
| chr6:47534916
|
TACTGA | T | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.319+1162_319+1166d others(7): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47534916 | ||||||
| chr6:47535062
|
G | T | 4 | a0001c0001t0022g0290a0001c0001t0022g0300a0001c0001t0052g0301others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+1307G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47535062 | ||||||
| chr6:47535077
|
G | A | 3 | a0001c0001t0019g0039a0001c0001t0019g0061a0001c0001t0019g0084 | 3 | NA18975.hp2 NA19000.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.319+1322G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47535077 | ||||||
| chr6:47535414
|
T | C | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.319+1659T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47535414 | ||||||
| chr6:47535567
|
G | A | 169 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.319+1812G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47535567 | ||||||
| chr6:47535761
|
A | T | 84 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.319+2006A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47535761 | ||||||
| chr6:47535767
|
A | G | 1 | a0001c0001t0003g0089 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.319+2012A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47535767 | ||||||
| chr6:47535804
|
C | T | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.319+2049C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47535804 | ||||||
| chr6:47535827
|
C | T | 2 | a0001c0001t0017g0042a0001c0001t0017g0044 | 2 | NA18954.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.319+2072C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47535827 | ||||||
| chr6:47535898
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.319+2143A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47535898 | ||||||
| chr6:47535973
|
A | G | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.319+2218A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47535973 | ||||||
| chr6:47536226
|
AT | A | 11 | a0001c0001t0001g0212a0001c0001t0001g0226a0001c0001t0001g0227others(8): Show | 11 | HG00642.hp1 HG00741.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.319+2484delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 47536226 | |||||
| chr6:47536294
|
G | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.319+2539G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47536294 | ||||||
| chr6:47536312
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.319+2557A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47536312 | ||||||
| chr6:47536378
|
T | C | 1 | a0001c0001t0006g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.319+2623T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47536378 | ||||||
| chr6:47536383
|
T | G | 2 | a0001c0001t0004g0319a0001c0001t0024g0142 | 2 | NA18968.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.319+2628T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47536383 | ||||||
| chr6:47536402
|
A | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.319+2647A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47536402 | ||||||
| chr6:47536596
|
A | G | 2 | a0001c0001t0021g0229a0001c0001t0021g0230 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.319+2841A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47536596 | ||||||
| chr6:47536603
|
C | T | 1 | a0001c0003t0044g0320 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.319+2848C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47536603 | ||||||
| chr6:47536660
|
A | G | 169 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.319+2905A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47536660 | ||||||
| chr6:47536777
|
A | G | 1 | a0001c0001t0038g0051 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.319+3022A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47536777 | ||||||
| chr6:47536964
|
C | CA | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+3210dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 47536964 | |||||
| chr6:47537014
|
G | A | 1 | a0001c0001t0031g0297 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.319+3259G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47537014 | ||||||
| chr6:47537019
|
C | G | 3 | a0001c0001t0005g0271a0001c0001t0005g0272a0001c0001t0011g0253 | 3 | HG01358.hp1 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.319+3264C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47537019 | ||||||
| chr6:47537100
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.319+3345C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47537100 | ||||||
| chr6:47537274
|
C | T | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.319+3519C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47537274 | ||||||
| chr6:47537438
|
C | G | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.319+3683C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47537438 | ||||||
| chr6:47537481
|
G | A | 169 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.319+3726G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47537481 | ||||||
| chr6:47537540
|
G | T | 1 | a0001c0001t0082g0145 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.319+3785G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47537540 | ||||||
| chr6:47537626
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.319+3871A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47537626 | ||||||
| chr6:47537851
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.319+4096A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47537851 | ||||||
| chr6:47537872
|
C | G | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.319+4117C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47537872 | ||||||
| chr6:47537934
|
AG | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0249a0001c0001t0001g0283others(1): Show | 4 | HG00323.hp1 HG01109.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+4180delG | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47537934 | ||||||
| chr6:47538045
|
C | T | 10 | a0001c0001t0016g0292a0001c0001t0016g0295a0001c0001t0016g0296others(7): Show | 10 | HG01069.hp2 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.319+4290C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47538045 | ||||||
| chr6:47538051
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.319+4296A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47538051 | ||||||
| chr6:47538179
|
C | T | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.319+4424C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47538179 | ||||||
| chr6:47538197
|
T | G | 163 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.319+4442T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47538197 | ||||||
| chr6:47538452
|
G | C | 3 | a0001c0001t0003g0017a0001c0001t0009g0048a0001c0001t0018g0082 | 3 | HG02809.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.319+4697G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47538452 | ||||||
| chr6:47538614
|
A | G | 75 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.319+4859A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47538614 | ||||||
| chr6:47539055
|
A | G | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+5300A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47539055 | ||||||
| chr6:47539218
|
A | C | 1 | a0001c0001t0011g0259 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.320-5388A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47539218 | ||||||
| chr6:47539225
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.320-5381C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47539225 | ||||||
| chr6:47539335
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.320-5271A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47539335 | ||||||
| chr6:47539420
|
C | A | 2 | a0001c0001t0002g0038a0001c0001t0002g0060 | 2 | HG01346.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.320-5186C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47539420 | ||||||
| chr6:47539439
|
A | G | 1 | a0001c0001t0010g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.320-5167A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47539439 | ||||||
| chr6:47539572
|
C | T | 1 | a0001c0003t0044g0320 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.320-5034C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47539572 | ||||||
| chr6:47539672
|
T | C | 1 | a0001c0001t0010g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.320-4934T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47539672 | ||||||
| chr6:47540014
|
C | CA | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.320-4581dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 47540014 | |||||
| chr6:47540044
|
A | G | 39 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(36): Show | 39 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.320-4562A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47540044 | ||||||
| chr6:47540174
|
C | CA | 32 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0003g0017others(29): Show | 32 | HG00741.hp1 HG01168.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.320-4413dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 47540174 | |||||
| chr6:47540174
|
CA | C | 6 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0002g0062others(3): Show | 6 | HG01069.hp2 HG01496.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-4413delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 47540174 | |||||
| chr6:47540187
|
A | G | 1 | a0001c0001t0011g0265 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.320-4419A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47540187 | ||||||
| chr6:47540619
|
T | C | 4 | a0001c0001t0008g0166a0001c0001t0008g0169a0001c0001t0008g0170others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.320-3987T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47540619 | ||||||
| chr6:47540735
|
T | C | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.320-3871T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47540735 | ||||||
| chr6:47541001
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.320-3605C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47541001 | ||||||
| chr6:47541146
|
C | T | 1 | a0001c0001t0071g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.320-3460C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47541146 | ||||||
| chr6:47541209
|
C | T | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.320-3397C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47541209 | ||||||
| chr6:47541376
|
G | A | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.320-3230G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47541376 | ||||||
| chr6:47541379
|
C | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.320-3227C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47541379 | ||||||
| chr6:47541388
|
T | G | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.320-3218T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47541388 | ||||||
| chr6:47541609
|
A | G | 1 | a0001c0001t0006g0314 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.320-2997A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47541609 | ||||||
| chr6:47541673
|
G | A | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.320-2933G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47541673 | ||||||
| chr6:47542012
|
C | T | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.320-2594C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47542012 | ||||||
| chr6:47542164
|
T | C | 3 | a0001c0001t0019g0039a0001c0001t0019g0061a0001c0001t0019g0084 | 3 | NA18975.hp2 NA19000.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.320-2442T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47542164 | ||||||
| chr6:47542227
|
A | T | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.320-2379A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47542227 | ||||||
| chr6:47542456
|
G | T | 2 | a0001c0001t0017g0004a0001c0001t0019g0003 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.320-2150G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47542456 | ||||||
| chr6:47542514
|
TCTCATGA others(24): Show |
T | 1 | a0001c0001t0072g0007 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.320-2090_320-2060d others(33): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 47542514 | |||||
| chr6:47542548
|
G | T | 1 | a0001c0001t0072g0007 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.320-2058G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47542548 | ||||||
| chr6:47542704
|
C | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.320-1902C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47542704 | ||||||
| chr6:47542718
|
T | C | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.320-1888T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47542718 | ||||||
| chr6:47543148
|
C | CA | 38 | a0001c0001t0002g0034a0001c0001t0006g0167a0001c0001t0006g0179others(35): Show | 38 | HG00099.hp1 HG00741.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.320-1434dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 47543148 | |||||
| chr6:47543148
|
C | CAA | 10 | a0001c0001t0006g0183a0001c0001t0006g0316a0001c0001t0008g0174others(7): Show | 10 | HG00735.hp1 HG01106.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.320-1435_320-1434d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 47543148 | |||||
| chr6:47543148
|
CA | C | 161 | a0001c0001t0001g0213a0001c0001t0001g0243a0001c0001t0001g0254others(158): Show | 161 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.320-1434delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 47543148 | |||||
| chr6:47543180
|
AAAAAAG | A | 70 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(67): Show | 70 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.320-1420_320-1415d others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 47543180 | |||||
| chr6:47543185
|
A | G | 5 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0011g0253others(2): Show | 5 | HG01255.hp1 HG02055.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-1421A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47543185 | ||||||
| chr6:47543186
|
G | A | 11 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0011g0253others(8): Show | 11 | HG01255.hp1 HG02055.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.320-1420G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47543186 | ||||||
| chr6:47543198
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.320-1408A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47543198 | ||||||
| chr6:47543353
|
G | A | 3 | a0001c0001t0036g0158a0001c0001t0036g0159a0001c0001t0084g0160 | 3 | HG02055.hp2 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.320-1253G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47543353 | ||||||
| chr6:47543448
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.320-1158A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47543448 | ||||||
| chr6:47543582
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.320-1024A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47543582 | ||||||
| chr6:47543587
|
C | G | 1 | a0001c0001t0100g0187 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.320-1019C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47543587 | ||||||
| chr6:47543755
|
A | G | 52 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(49): Show | 52 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.320-851A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47543755 | ||||||
| chr6:47543891
|
T | C | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.320-715T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47543891 | ||||||
| chr6:47544032
|
C | T | 1 | a0001c0001t0058g0130 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.320-574C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47544032 | ||||||
| chr6:47544110
|
TGA | T | 78 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(75): Show | 78 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.320-494_320-493del others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 47544110 | |||||
| chr6:47544275
|
T | C | 1 | a0001c0001t0078g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.320-331T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47544275 | ||||||
| chr6:47544420
|
A | C | 1 | a0001c0001t0035g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.320-186A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47544420 | ||||||
| chr6:47544493
|
C | T | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.320-113C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 3/17 | chr6 | 47544493 | ||||||
| chr6:47544777
|
G | A | 1 | a0001c0001t0013g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.420+71G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47544777 | ||||||
| chr6:47544829
|
T | G | 1 | a0001c0001t0028g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.420+123T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47544829 | ||||||
| chr6:47544854
|
C | T | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.420+148C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47544854 | ||||||
| chr6:47545340
|
A | G | 169 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.420+634A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47545340 | ||||||
| chr6:47545468
|
A | C | 264 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(261): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.420+762A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47545468 | ||||||
| chr6:47545542
|
A | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+836A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47545542 | ||||||
| chr6:47545616
|
T | C | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.420+910T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47545616 | ||||||
| chr6:47545725
|
G | A | 4 | a0001c0001t0027g0119a0001c0001t0027g0126a0001c0001t0046g0118others(1): Show | 4 | HG01975.hp2 HG01981.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+1019G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47545725 | ||||||
| chr6:47545780
|
C | T | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.420+1074C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47545780 | ||||||
| chr6:47545859
|
G | T | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.420+1153G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47545859 | ||||||
| chr6:47546012
|
T | G | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.420+1306T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47546012 | ||||||
| chr6:47546510
|
T | A | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.420+1804T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47546510 | ||||||
| chr6:47546543
|
A | G | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.420+1837A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47546543 | ||||||
| chr6:47546633
|
C | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.420+1927C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47546633 | ||||||
| chr6:47546651
|
A | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.420+1945A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47546651 | ||||||
| chr6:47547022
|
G | A | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.420+2316G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547022 | ||||||
| chr6:47547064
|
C | G | 13 | a0001c0001t0005g0216a0001c0001t0005g0217a0001c0001t0005g0219others(10): Show | 13 | NA18612.hp1 NA18953.hp2 NA18975.hp1 others(10): Show |
intron_variant | MODIFIER | c.420+2358C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547064 | ||||||
| chr6:47547081
|
A | G | 1 | a0001c0001t0071g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.420+2375A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547081 | ||||||
| chr6:47547187
|
T | C | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.420+2481T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547187 | ||||||
| chr6:47547206
|
A | G | 1 | a0001c0001t0046g0118 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.420+2500A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547206 | ||||||
| chr6:47547462
|
G | A | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.420+2756G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547462 | ||||||
| chr6:47547464
|
C | A | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.420+2758C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547464 | ||||||
| chr6:47547486
|
C | CTA | 84 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.420+2792_420+2793d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47547486 | |||||
| chr6:47547523
|
G | A | 165 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.420+2817G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547523 | ||||||
| chr6:47547524
|
T | A | 1 | a0001c0001t0014g0151 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.420+2818T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547524 | ||||||
| chr6:47547539
|
G | A | 1 | a0004c0006t0040g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.420+2833G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547539 | ||||||
| chr6:47547690
|
A | G | 1 | a0001c0001t0020g0175 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.420+2984A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547690 | ||||||
| chr6:47547784
|
A | G | 1 | a0001c0001t0005g0255 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.420+3078A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547784 | ||||||
| chr6:47547894
|
G | A | 80 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.420+3188G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547894 | ||||||
| chr6:47547927
|
T | C | 84 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.420+3221T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547927 | ||||||
| chr6:47547982
|
A | G | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.420+3276A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47547982 | ||||||
| chr6:47548075
|
A | G | 63 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.420+3369A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47548075 | ||||||
| chr6:47548633
|
A | G | 81 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(78): Show | 81 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.420+3927A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47548633 | ||||||
| chr6:47549032
|
T | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.420+4326T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47549032 | ||||||
| chr6:47549091
|
A | G | 3 | a0001c0001t0004g0114a0001c0001t0004g0132a0001c0001t0034g0140 | 3 | HG00140.hp2 HG01346.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.420+4385A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47549091 | ||||||
| chr6:47549182
|
A | C | 3 | a0001c0001t0005g0271a0001c0001t0005g0272a0001c0001t0011g0253 | 3 | HG01358.hp1 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.420+4476A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47549182 | ||||||
| chr6:47549260
|
A | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.420+4554A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47549260 | ||||||
| chr6:47549460
|
C | CA | 47 | a0001c0001t0001g0208a0001c0001t0001g0225a0001c0001t0001g0234others(44): Show | 47 | HG00099.hp1 HG00735.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.420+4774dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47549460 | |||||
| chr6:47549460
|
C | CAA | 63 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0215others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.420+4773_420+4774d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47549460 | |||||
| chr6:47549460
|
C | CAAA | 10 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0256others(7): Show | 10 | HG01255.hp2 HG02056.hp2 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.420+4772_420+4774d others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47549460 | |||||
| chr6:47549460
|
CA | C | 81 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(78): Show | 81 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.420+4774delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47549460 | |||||
| chr6:47549460
|
CAA | C | 69 | a0001c0001t0004g0110a0001c0001t0004g0114a0001c0001t0004g0123others(66): Show | 69 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.420+4773_420+4774d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47549460 | |||||
| chr6:47549460
|
CAAA | C | 13 | a0001c0001t0016g0295a0001c0001t0016g0296a0001c0001t0027g0119others(10): Show | 13 | HG01069.hp2 HG01891.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.420+4772_420+4774d others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47549460 | |||||
| chr6:47549539
|
C | T | 39 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(36): Show | 39 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.420+4833C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47549539 | ||||||
| chr6:47549562
|
A | G | 39 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(36): Show | 39 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.420+4856A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47549562 | ||||||
| chr6:47549733
|
A | G | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.421-4913A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47549733 | ||||||
| chr6:47549930
|
G | A | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.421-4716G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47549930 | ||||||
| chr6:47550094
|
A | G | 8 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0071others(5): Show | 8 | NA18942.hp1 NA18946.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.421-4552A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47550094 | ||||||
| chr6:47550239
|
G | T | 1 | a0007c0009t0099g0190 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.421-4407G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47550239 | ||||||
| chr6:47550732
|
CAT | C | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-3913_421-3912d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47550732 | ||||||
| chr6:47550735
|
G | A | 78 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(75): Show | 78 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.421-3911G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47550735 | ||||||
| chr6:47550793
|
G | A | 308 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(305): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.421-3853G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47550793 | ||||||
| chr6:47550878
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.421-3768C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47550878 | ||||||
| chr6:47551185
|
TAAAAAA | T | 97 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(94): Show | 97 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.421-3458_421-3453d others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47551185 | |||||
| chr6:47551195
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.421-3451A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47551195 | ||||||
| chr6:47551203
|
A | T | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.421-3443A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47551203 | ||||||
| chr6:47551230
|
T | G | 1 | a0005c0007t0005g0224 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.421-3416T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47551230 | ||||||
| chr6:47551277
|
CAT | C | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.421-3368_421-3367d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47551277 | ||||||
| chr6:47551328
|
T | G | 1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.421-3318T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47551328 | ||||||
| chr6:47551383
|
A | C | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.421-3263A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47551383 | ||||||
| chr6:47551585
|
G | A | 165 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.421-3061G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47551585 | ||||||
| chr6:47551745
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.421-2901G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47551745 | ||||||
| chr6:47551962
|
C | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-2684C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47551962 | ||||||
| chr6:47552055
|
G | T | 1 | a0001c0001t0003g0045 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.421-2591G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47552055 | ||||||
| chr6:47552072
|
T | C | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.421-2574T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47552072 | ||||||
| chr6:47552181
|
AGGT | A | 5 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0062others(2): Show | 5 | HG01109.hp1 HG01496.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.421-2460_421-2458d others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47552181 | |||||
| chr6:47552330
|
A | G | 1 | a0001c0001t0006g0318 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.421-2316A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47552330 | ||||||
| chr6:47552366
|
A | G | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.421-2280A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47552366 | ||||||
| chr6:47552666
|
C | T | 1 | a0001c0001t0075g0010 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.421-1980C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47552666 | ||||||
| chr6:47552743
|
A | T | 1 | a0001c0001t0010g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.421-1903A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47552743 | ||||||
| chr6:47552887
|
A | G | 2 | a0001c0001t0003g0063a0001c0001t0009g0065 | 2 | NA18612.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.421-1759A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47552887 | ||||||
| chr6:47552990
|
A | AT | 84 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.421-1646dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47552990 | |||||
| chr6:47553096
|
A | T | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.421-1550A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47553096 | ||||||
| chr6:47553320
|
A | C | 5 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0062others(2): Show | 5 | HG01109.hp1 HG01496.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.421-1326A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47553320 | ||||||
| chr6:47553351
|
G | GT | 18 | a0001c0001t0006g0315a0001c0001t0016g0291a0001c0001t0016g0292others(15): Show | 18 | HG01069.hp2 HG01168.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.421-1282dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47553351 | |||||
| chr6:47553352
|
T | G | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.421-1294T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47553352 | ||||||
| chr6:47553399
|
A | G | 1 | a0001c0001t0070g0009 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.421-1247A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47553399 | ||||||
| chr6:47553481
|
G | A | 2 | a0001c0001t0071g0205a0001c0001t0076g0206 | 2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.421-1165G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47553481 | ||||||
| chr6:47553499
|
A | T | 31 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(28): Show | 31 | HG00597.hp2 HG00733.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.421-1147A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47553499 | ||||||
| chr6:47553503
|
C | T | 2 | a0001c0001t0030g0302a0002c0002t0001g0281 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.421-1143C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47553503 | ||||||
| chr6:47553513
|
A | AT | 23 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0023others(20): Show | 23 | HG00733.hp2 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.421-1109dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47553513 | |||||
| chr6:47553513
|
AT | A | 75 | a0001c0001t0002g0036a0001c0001t0004g0105a0001c0001t0004g0114others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.421-1109delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47553513 | |||||
| chr6:47553513
|
ATTTTTT | A | 71 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(68): Show | 71 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.421-1114_421-1109d others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47553513 | |||||
| chr6:47553513
|
ATTTTTTT | A | 7 | a0001c0001t0001g0234a0001c0001t0028g0209a0001c0001t0028g0210others(4): Show | 7 | HG01255.hp2 HG02630.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-1115_421-1109d others(9): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 47553513 | |||||
| chr6:47553943
|
G | A | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.421-703G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47553943 | ||||||
| chr6:47554016
|
C | G | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.421-630C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47554016 | ||||||
| chr6:47554053
|
C | T | 1 | a0001c0001t0002g0036 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.421-593C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47554053 | ||||||
| chr6:47554371
|
T | C | 1 | a0001c0001t0006g0183 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.421-275T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47554371 | ||||||
| chr6:47554494
|
A | G | 1 | a0001c0001t0004g0129 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.421-152A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47554494 | ||||||
| chr6:47554621
|
G | A | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.421-25G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 4/17 | chr6 | 47554621 | ||||||
| chr6:47554785
|
T | A | 2 | a0001c0001t0016g0292a0001c0001t0029g0293 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.541+19T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47554785 | ||||||
| chr6:47554915
|
G | A | 2 | a0001c0001t0036g0158a0001c0001t0084g0160 | 2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.541+149G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47554915 | ||||||
| chr6:47555366
|
A | C | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.541+600A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47555366 | ||||||
| chr6:47555503
|
A | G | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.541+737A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47555503 | ||||||
| chr6:47555539
|
C | G | 2 | a0001c0001t0017g0004a0001c0001t0019g0003 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.541+773C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47555539 | ||||||
| chr6:47555804
|
A | AT | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.541+1048dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47555804 | |||||
| chr6:47555870
|
T | TC | 83 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.541+1105dupC | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47555870 | |||||
| chr6:47555877
|
T | C | 1 | a0001c0001t0004g0123 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.541+1111T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47555877 | ||||||
| chr6:47556055
|
CT | C | 102 | a0001c0001t0001g0273a0001c0001t0002g0006a0001c0001t0002g0008others(99): Show | 102 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.541+1305delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47556055 | |||||
| chr6:47556139
|
C | T | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.541+1373C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556139 | ||||||
| chr6:47556208
|
C | T | 1 | a0001c0001t0033g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.541+1442C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556208 | ||||||
| chr6:47556261
|
C | A | 4 | a0001c0001t0023g0198a0001c0001t0023g0202a0001c0001t0023g0203others(1): Show | 4 | HG00741.hp1 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+1495C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556261 | ||||||
| chr6:47556322
|
C | G | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.541+1556C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556322 | ||||||
| chr6:47556389
|
CT | C | 165 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.541+1634delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47556389 | |||||
| chr6:47556442
|
A | G | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.541+1676A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556442 | ||||||
| chr6:47556470
|
C | A | 1 | a0001c0001t0041g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.541+1704C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556470 | ||||||
| chr6:47556595
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.541+1829C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556595 | ||||||
| chr6:47556612
|
G | T | 2 | a0001c0001t0019g0039a0001c0001t0019g0084 | 2 | NA19000.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.541+1846G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556612 | ||||||
| chr6:47556638
|
T | G | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.541+1872T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556638 | ||||||
| chr6:47556785
|
A | ATG | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+2031_541+2032d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47556785 | |||||
| chr6:47556829
|
G | A | 2 | a0001c0001t0012g0201a0001c0001t0066g0199 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.541+2063G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556829 | ||||||
| chr6:47556848
|
G | A | 5 | a0001c0001t0016g0295a0001c0001t0016g0296a0001c0001t0029g0289others(2): Show | 5 | HG01069.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+2082G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556848 | ||||||
| chr6:47556903
|
G | A | 1 | a0001c0001t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.541+2137G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556903 | ||||||
| chr6:47556939
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.541+2173G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556939 | ||||||
| chr6:47556953
|
T | C | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.541+2187T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47556953 | ||||||
| chr6:47557031
|
A | T | 1 | a0001c0001t0007g0153 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.541+2265A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47557031 | ||||||
| chr6:47557033
|
G | A | 91 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(88): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.541+2267G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47557033 | ||||||
| chr6:47557169
|
G | GT | 87 | a0001c0001t0004g0105a0001c0001t0004g0114a0001c0001t0004g0123others(84): Show | 87 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.541+2417dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47557169 | |||||
| chr6:47557169
|
G | GTT | 78 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(75): Show | 78 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.541+2416_541+2417d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47557169 | |||||
| chr6:47557318
|
T | G | 1 | a0001c0001t0011g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.541+2552T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47557318 | ||||||
| chr6:47557466
|
G | A | 84 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.541+2700G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47557466 | ||||||
| chr6:47557568
|
T | C | 2 | a0001c0001t0017g0004a0001c0001t0019g0003 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.541+2802T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47557568 | ||||||
| chr6:47557593
|
C | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+2827C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47557593 | ||||||
| chr6:47558053
|
G | A | 1 | a0001c0001t0002g0034 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.541+3287G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47558053 | ||||||
| chr6:47558343
|
G | A | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.541+3577G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47558343 | ||||||
| chr6:47558383
|
A | G | 1 | a0001c0001t0004g0114 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.541+3617A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47558383 | ||||||
| chr6:47558387
|
C | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.541+3621C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47558387 | ||||||
| chr6:47558534
|
A | G | 1 | a0001c0008t0001g0244 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.541+3768A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47558534 | ||||||
| chr6:47558608
|
A | G | 5 | a0001c0001t0016g0295a0001c0001t0016g0296a0001c0001t0029g0289others(2): Show | 5 | HG01069.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+3842A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47558608 | ||||||
| chr6:47558681
|
T | C | 306 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.541+3915T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47558681 | ||||||
| chr6:47558748
|
A | T | 1 | a0003c0004t0061g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.541+3982A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47558748 | ||||||
| chr6:47558771
|
G | C | 73 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.541+4005G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47558771 | ||||||
| chr6:47558991
|
T | C | 1 | a0001c0001t0018g0055 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.541+4225T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47558991 | ||||||
| chr6:47559021
|
A | G | 1 | a0001c0001t0009g0020 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.541+4255A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47559021 | ||||||
| chr6:47559067
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.541+4301C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47559067 | ||||||
| chr6:47559257
|
AT | A | 16 | a0001c0001t0002g0074a0001c0001t0005g0216a0001c0001t0016g0292others(13): Show | 16 | HG00642.hp2 HG02257.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.541+4509delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47559257 | |||||
| chr6:47559261
|
T | G | 1 | a0001c0001t0001g0212 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.541+4495T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47559261 | ||||||
| chr6:47559301
|
C | T | 6 | a0001c0001t0001g0212a0001c0001t0001g0226a0001c0001t0001g0227others(3): Show | 6 | HG00642.hp1 HG01255.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.541+4535C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47559301 | ||||||
| chr6:47559307
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.541+4541T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47559307 | ||||||
| chr6:47559886
|
A | G | 1 | a0001c0001t0057g0288 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.541+5120A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47559886 | ||||||
| chr6:47560027
|
A | G | 91 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(88): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.541+5261A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47560027 | ||||||
| chr6:47560092
|
CT | C | 68 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.541+5334delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47560092 | |||||
| chr6:47560800
|
C | T | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.541+6034C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47560800 | ||||||
| chr6:47560895
|
A | C | 2 | a0001c0001t0012g0322a0001c0001t0048g0321 | 2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.541+6129A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47560895 | ||||||
| chr6:47560929
|
T | C | 1 | a0001c0001t0003g0053 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.541+6163T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47560929 | ||||||
| chr6:47560970
|
G | A | 1 | a0001c0001t0089g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.541+6204G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47560970 | ||||||
| chr6:47561028
|
C | G | 81 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(78): Show | 81 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.541+6262C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561028 | ||||||
| chr6:47561033
|
G | A | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.541+6267G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561033 | ||||||
| chr6:47561051
|
G | A | 2 | a0001c0001t0023g0202a0001c0001t0023g0203 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.541+6285G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561051 | ||||||
| chr6:47561081
|
T | G | 306 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.541+6315T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561081 | ||||||
| chr6:47561147
|
C | A | 1 | a0001c0001t0073g0075 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.541+6381C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561147 | ||||||
| chr6:47561158
|
C | T | 2 | a0001c0001t0077g0113a0001c0001t0088g0112 | 2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.541+6392C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561158 | ||||||
| chr6:47561186
|
A | G | 2 | a0001c0001t0034g0107a0001c0001t0052g0301 | 2 | HG03195.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.541+6420A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561186 | ||||||
| chr6:47561306
|
A | C | 6 | a0002c0002t0001g0276a0002c0002t0001g0277a0002c0002t0001g0278others(3): Show | 6 | HG01243.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.541+6540A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561306 | ||||||
| chr6:47561396
|
T | C | 3 | a0001c0001t0002g0081a0001c0001t0002g0096a0001c0001t0013g0091 | 3 | NA18986.hp1 NA19059.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.541+6630T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561396 | ||||||
| chr6:47561462
|
T | A | 1 | a0001c0001t0020g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.541+6696T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561462 | ||||||
| chr6:47561550
|
T | C | 2 | a0001c0001t0004g0319a0001c0001t0024g0142 | 2 | NA18968.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.541+6784T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561550 | ||||||
| chr6:47561811
|
C | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+7045C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561811 | ||||||
| chr6:47561932
|
C | T | 2 | a0001c0001t0002g0081a0001c0001t0013g0091 | 2 | NA18986.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.541+7166C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561932 | ||||||
| chr6:47561999
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.541+7233C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47561999 | ||||||
| chr6:47562079
|
T | C | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.541+7313T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47562079 | ||||||
| chr6:47562208
|
G | T | 2 | a0001c0001t0021g0229a0001c0001t0021g0230 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.541+7442G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47562208 | ||||||
| chr6:47562403
|
G | A | 318 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.541+7637G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47562403 | ||||||
| chr6:47562592
|
T | G | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.541+7826T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47562592 | ||||||
| chr6:47562686
|
A | C | 306 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.541+7920A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47562686 | ||||||
| chr6:47562769
|
G | C | 1 | a0001c0001t0091g0005 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.541+8003G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47562769 | ||||||
| chr6:47562979
|
C | G | 167 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(164): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.541+8213C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47562979 | ||||||
| chr6:47562979
|
C | T | 97 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(94): Show | 97 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.541+8213C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47562979 | ||||||
| chr6:47563078
|
T | C | 1 | a0001c0001t0009g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.541+8312T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47563078 | ||||||
| chr6:47563100
|
G | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.541+8334G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47563100 | ||||||
| chr6:47563559
|
A | G | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.541+8793A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47563559 | ||||||
| chr6:47563587
|
T | G | 1 | a0001c0001t0083g0157 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.541+8821T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47563587 | ||||||
| chr6:47563619
|
C | T | 1 | a0001c0001t0057g0288 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.541+8853C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47563619 | ||||||
| chr6:47563882
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.541+9116C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47563882 | ||||||
| chr6:47563944
|
A | G | 2 | a0001c0001t0064g0284a0003c0004t0032g0312 | 2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.541+9178A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47563944 | ||||||
| chr6:47563986
|
T | A | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.541+9220T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47563986 | ||||||
| chr6:47563998
|
T | C | 3 | a0001c0001t0035g0103a0001c0001t0079g0104a0001c0001t0087g0102 | 3 | HG02451.hp2 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.541+9232T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47563998 | ||||||
| chr6:47564009
|
T | C | 1 | a0001c0001t0028g0210 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.541+9243T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47564009 | ||||||
| chr6:47564056
|
T | A | 1 | a0001c0001t0004g0132 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.541+9290T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47564056 | ||||||
| chr6:47564142
|
T | G | 1 | a0001c0001t0014g0121 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.541+9376T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47564142 | ||||||
| chr6:47564153
|
C | T | 2 | a0001c0001t0075g0010a0001c0001t0078g0011 | 2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.541+9387C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47564153 | ||||||
| chr6:47564320
|
A | AGT | 8 | a0001c0001t0022g0290a0001c0001t0022g0300a0001c0001t0022g0305others(5): Show | 8 | HG02258.hp1 HG02717.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.541+9556_541+9557d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47564320 | |||||
| chr6:47564347
|
A | T | 1 | a0001c0001t0035g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.541+9581A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47564347 | ||||||
| chr6:47564550
|
C | G | 1 | a0001c0001t0018g0014 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.542-9514C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47564550 | ||||||
| chr6:47564694
|
G | A | 1 | a0001c0001t0075g0010 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.542-9370G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47564694 | ||||||
| chr6:47564818
|
G | A | 1 | a0004c0006t0040g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.542-9246G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47564818 | ||||||
| chr6:47564861
|
G | GTTT | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.542-9201_542-9199d others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47564861 | |||||
| chr6:47564896
|
T | C | 1 | a0001c0001t0037g0116 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.542-9168T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47564896 | ||||||
| chr6:47564908
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.542-9156G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47564908 | ||||||
| chr6:47564947
|
T | A | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.542-9117T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47564947 | ||||||
| chr6:47565241
|
C | T | 1 | a0001c0001t0013g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.542-8823C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47565241 | ||||||
| chr6:47565461
|
A | G | 3 | a0001c0001t0006g0316a0001c0001t0006g0317a0001c0001t0006g0318 | 3 | NA18946.hp2 NA18966.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.542-8603A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47565461 | ||||||
| chr6:47565864
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.542-8200C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47565864 | ||||||
| chr6:47565905
|
T | C | 2 | a0001c0001t0006g0167a0001c0001t0008g0310 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.542-8159T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47565905 | ||||||
| chr6:47566301
|
A | AAT | 39 | a0001c0001t0003g0045a0001c0001t0006g0180a0001c0001t0006g0183others(36): Show | 39 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.542-7741_542-7740d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566301 | |||||
| chr6:47566301
|
A | AATAT | 84 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(81): Show | 84 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.542-7743_542-7740d others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566301 | |||||
| chr6:47566301
|
A | AATATAT | 8 | a0001c0001t0003g0043a0001c0001t0003g0067a0001c0001t0006g0179others(5): Show | 8 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(5): Show |
intron_variant | MODIFIER | c.542-7745_542-7740d others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566301 | |||||
| chr6:47566301
|
A | AATATATA others(1): Show |
4 | a0001c0001t0002g0034a0001c0001t0017g0042a0001c0001t0026g0052others(1): Show | 4 | HG00642.hp2 NA18955.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-7747_542-7740d others(10): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566301 | |||||
| chr6:47566301
|
A | AATATATA others(11): Show |
1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.542-7757_542-7740d others(20): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566301 | |||||
| chr6:47566301
|
AATATATA others(3): Show |
A | 82 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.542-7749_542-7740d others(12): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566301 | |||||
| chr6:47566323
|
T | C | 1 | a0001c0001t0011g0265 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.542-7741T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47566323 | ||||||
| chr6:47566323
|
T | TATACACA others(5): Show |
1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.542-7740_542-7739i others(14): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATACA others(5): Show |
1 | a0001c0001t0001g0245 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.542-7740_542-7739i others(14): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATACA others(19): Show |
1 | a0001c0001t0055g0098 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.542-7740_542-7739i others(28): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.542-7740_542-7739i others(16): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(21): Show |
1 | a0001c0001t0053g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.542-7740_542-7739i others(30): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(11): Show |
4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-7740_542-7739i others(20): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(13): Show |
1 | a0001c0001t0001g0274 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.542-7740_542-7739i others(22): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(15): Show |
2 | a0001c0001t0005g0221a0001c0001t0015g0222 | 2 | NA18988.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.542-7740_542-7739i others(24): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(15): Show |
2 | a0001c0001t0011g0253a0002c0002t0001g0277 | 2 | HG03471.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.542-7740_542-7739i others(24): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(17): Show |
5 | a0001c0001t0005g0216a0001c0001t0005g0217a0001c0001t0005g0219others(2): Show | 5 | NA18612.hp1 NA18953.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.542-7740_542-7739i others(26): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(21): Show |
1 | a0001c0001t0001g0215 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.542-7740_542-7739i others(30): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(17): Show |
3 | a0001c0001t0001g0249a0001c0001t0005g0272a0001c0001t0011g0259 | 3 | HG01109.hp2 HG02056.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.542-7740_542-7739i others(26): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(19): Show |
8 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0001g0266others(5): Show | 8 | HG01123.hp2 HG01243.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.542-7740_542-7739i others(28): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(21): Show |
2 | a0001c0001t0001g0243a0001c0001t0011g0250 | 2 | HG01074.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.542-7740_542-7739i others(30): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(23): Show |
2 | a0001c0001t0021g0229a0001c0001t0021g0230 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.542-7740_542-7739i others(32): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(21): Show |
7 | a0001c0001t0001g0213a0001c0001t0001g0239a0001c0001t0001g0283others(4): Show | 7 | HG00323.hp1 HG01261.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.542-7740_542-7739i others(30): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(23): Show |
6 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0233others(3): Show | 6 | HG01256.hp1 HG01258.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.542-7740_542-7739i others(32): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(23): Show |
2 | a0001c0001t0001g0225a0001c0001t0001g0236 | 2 | NA18961.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.542-7740_542-7739i others(32): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(25): Show |
2 | a0001c0001t0015g0262a0005c0007t0005g0224 | 2 | NA18999.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.542-7740_542-7739i others(34): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(25): Show |
4 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0237others(1): Show | 4 | HG04228.hp1 NA18943.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-7740_542-7739i others(34): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(27): Show |
2 | a0001c0001t0001g0258a0001c0001t0001g0275 | 2 | HG01934.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.542-7740_542-7739i others(36): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(27): Show |
1 | a0001c0001t0001g0208 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.542-7740_542-7739i others(36): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(29): Show |
8 | a0001c0001t0001g0212a0001c0001t0001g0232a0001c0001t0001g0242others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.542-7740_542-7739i others(38): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(31): Show |
2 | a0001c0001t0001g0223a0001c0001t0001g0228 | 2 | HG00280.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.542-7740_542-7739i others(40): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(29): Show |
1 | a0001c0001t0001g0268 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.542-7740_542-7739i others(38): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(31): Show |
2 | a0001c0001t0005g0241a0001c0001t0005g0260 | 2 | HG01433.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.542-7740_542-7739i others(40): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(31): Show |
1 | a0001c0001t0049g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.542-7740_542-7739i others(40): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(33): Show |
3 | a0001c0001t0001g0240a0001c0001t0011g0231a0001c0001t0015g0263 | 3 | HG01255.hp1 HG02300.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.542-7740_542-7739i others(42): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(33): Show |
2 | a0001c0001t0001g0267a0001c0001t0001g0270 | 2 | NA18951.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.542-7740_542-7739i others(42): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(35): Show |
2 | a0001c0001t0001g0273a0001c0008t0001g0244 | 2 | HG01928.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.542-7740_542-7739i others(44): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(35): Show |
1 | a0001c0001t0001g0238 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.542-7740_542-7739i others(44): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566323
|
T | TATATATA others(39): Show |
1 | a0001c0001t0001g0269 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.542-7740_542-7739i others(48): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47566323 | |||||
| chr6:47566329
|
T | C | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.542-7735T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47566329 | ||||||
| chr6:47566331
|
C | T | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.542-7733C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47566331 | ||||||
| chr6:47566335
|
T | C | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.542-7729T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47566335 | ||||||
| chr6:47566444
|
T | C | 1 | a0001c0001t0042g0192 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.542-7620T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47566444 | ||||||
| chr6:47566608
|
C | G | 1 | a0001c0001t0002g0040 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.542-7456C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47566608 | ||||||
| chr6:47566613
|
C | T | 1 | a0001c0001t0017g0044 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.542-7451C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47566613 | ||||||
| chr6:47566621
|
C | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.542-7443C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47566621 | ||||||
| chr6:47566691
|
A | G | 1 | a0001c0001t0025g0057 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.542-7373A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47566691 | ||||||
| chr6:47566928
|
C | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-7136C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47566928 | ||||||
| chr6:47567084
|
G | GT | 98 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(95): Show | 98 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.542-6967dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47567084 | |||||
| chr6:47567091
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.542-6973T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47567091 | ||||||
| chr6:47567327
|
C | T | 1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.542-6737C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47567327 | ||||||
| chr6:47567397
|
A | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.542-6667A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47567397 | ||||||
| chr6:47567472
|
A | C | 167 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(164): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.542-6592A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47567472 | ||||||
| chr6:47567591
|
G | A | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.542-6473G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47567591 | ||||||
| chr6:47567826
|
G | A | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.542-6238G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47567826 | ||||||
| chr6:47567901
|
A | C | 3 | a0001c0001t0037g0116a0001c0001t0037g0128a0001c0001t0093g0117 | 3 | HG02647.hp1 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.542-6163A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47567901 | ||||||
| chr6:47567950
|
G | A | 318 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.542-6114G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47567950 | ||||||
| chr6:47568068
|
G | A | 1 | a0001c0001t0009g0002 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.542-5996G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47568068 | ||||||
| chr6:47568187
|
G | A | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.542-5877G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47568187 | ||||||
| chr6:47568524
|
A | G | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.542-5540A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47568524 | ||||||
| chr6:47568594
|
A | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.542-5470A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47568594 | ||||||
| chr6:47568627
|
G | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.542-5437G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47568627 | ||||||
| chr6:47568708
|
C | T | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.542-5356C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47568708 | ||||||
| chr6:47568739
|
G | T | 2 | a0001c0001t0012g0322a0001c0001t0048g0321 | 2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.542-5325G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47568739 | ||||||
| chr6:47568743
|
C | CAAATAAA others(1): Show |
166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.542-5310_542-5303d others(10): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47568743 | |||||
| chr6:47568884
|
G | A | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.542-5180G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47568884 | ||||||
| chr6:47569156
|
A | T | 4 | a0001c0001t0023g0198a0001c0001t0023g0202a0001c0001t0023g0203others(1): Show | 4 | HG00741.hp1 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.542-4908A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47569156 | ||||||
| chr6:47569301
|
A | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.542-4763A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47569301 | ||||||
| chr6:47569406
|
G | A | 6 | a0001c0001t0001g0228a0001c0001t0001g0242a0001c0001t0001g0248others(3): Show | 6 | HG00639.hp2 HG01169.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.542-4658G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47569406 | ||||||
| chr6:47569576
|
A | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.542-4488A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47569576 | ||||||
| chr6:47569584
|
G | A | 1 | a0001c0001t0003g0067 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.542-4480G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47569584 | ||||||
| chr6:47569740
|
C | G | 1 | a0001c0001t0004g0136 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.542-4324C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47569740 | ||||||
| chr6:47569922
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.542-4142C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47569922 | ||||||
| chr6:47569989
|
A | G | 1 | a0001c0001t0009g0056 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.542-4075A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47569989 | ||||||
| chr6:47570141
|
CT | C | 68 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(65): Show | 68 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.542-3911delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47570141 | |||||
| chr6:47570209
|
T | C | 1 | a0001c0001t0002g0085 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.542-3855T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47570209 | ||||||
| chr6:47570278
|
A | G | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-3786A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47570278 | ||||||
| chr6:47570394
|
A | G | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.542-3670A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47570394 | ||||||
| chr6:47570540
|
CT | C | 318 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.542-3520delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47570540 | |||||
| chr6:47570615
|
TA | T | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.542-3447delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47570615 | |||||
| chr6:47570804
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.542-3260C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47570804 | ||||||
| chr6:47570872
|
G | A | 1 | a0001c0001t0021g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.542-3192G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47570872 | ||||||
| chr6:47571013
|
C | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.542-3051C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47571013 | ||||||
| chr6:47571389
|
G | A | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.542-2675G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47571389 | ||||||
| chr6:47571499
|
T | G | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.542-2565T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47571499 | ||||||
| chr6:47571566
|
G | T | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.542-2498G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47571566 | ||||||
| chr6:47571700
|
A | G | 1 | a0001c0001t0071g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.542-2364A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47571700 | ||||||
| chr6:47571750
|
G | T | 2 | a0001c0003t0012g0308a0001c0003t0012g0309 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.542-2314G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47571750 | ||||||
| chr6:47571858
|
TC | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.542-2204delC | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47571858 | |||||
| chr6:47571888
|
G | A | 1 | a0001c0001t0006g0315 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.542-2176G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47571888 | ||||||
| chr6:47572025
|
A | C | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.542-2039A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47572025 | ||||||
| chr6:47572081
|
A | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.542-1983A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47572081 | ||||||
| chr6:47572339
|
A | G | 1 | a0001c0001t0008g0178 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.542-1725A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47572339 | ||||||
| chr6:47572363
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.542-1701G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47572363 | ||||||
| chr6:47572375
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.542-1689C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47572375 | ||||||
| chr6:47572754
|
A | G | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.542-1310A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47572754 | ||||||
| chr6:47572800
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.542-1264C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47572800 | ||||||
| chr6:47572813
|
A | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.542-1251A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47572813 | ||||||
| chr6:47572977
|
G | T | 2 | a0001c0001t0004g0105a0001c0001t0010g0106 | 2 | NA18949.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.542-1087G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47572977 | ||||||
| chr6:47573013
|
T | C | 2 | a0001c0001t0017g0042a0001c0001t0017g0044 | 2 | NA18954.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.542-1051T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47573013 | ||||||
| chr6:47573101
|
A | T | 2 | a0001c0001t0002g0041a0001c0001t0003g0089 | 2 | NA19011.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.542-963A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47573101 | ||||||
| chr6:47573102
|
T | G | 2 | a0001c0001t0002g0041a0001c0001t0003g0089 | 2 | NA19011.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.542-962T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47573102 | ||||||
| chr6:47573119
|
G | A | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.542-945G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47573119 | ||||||
| chr6:47573484
|
G | GT | 100 | a0001c0001t0001g0208a0001c0001t0001g0240a0001c0001t0001g0252others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.542-558dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47573484 | |||||
| chr6:47573484
|
G | GTT | 12 | a0001c0001t0004g0105a0001c0001t0004g0125a0001c0001t0010g0127others(9): Show | 12 | HG00280.hp2 HG00423.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.542-559_542-558dup others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47573484 | |||||
| chr6:47573484
|
G | T | 1 | a0001c0001t0091g0005 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.542-580G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47573484 | ||||||
| chr6:47573484
|
GT | G | 13 | a0001c0001t0001g0245a0001c0001t0002g0038a0001c0001t0002g0068others(10): Show | 13 | HG00642.hp2 HG01346.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.542-558delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 47573484 | |||||
| chr6:47573550
|
G | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.542-514G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47573550 | ||||||
| chr6:47573613
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.542-451C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47573613 | ||||||
| chr6:47573645
|
T | C | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.542-419T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47573645 | ||||||
| chr6:47573679
|
C | G | 84 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.542-385C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47573679 | ||||||
| chr6:47573761
|
T | G | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.542-303T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 5/17 | chr6 | 47573761 | ||||||
| chr6:47574302
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.729+51A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47574302 | ||||||
| chr6:47574344
|
T | TC | 3 | a0001c0001t0006g0167a0001c0001t0008g0310a0001c0001t0042g0168 | 3 | HG01891.hp2 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.729+94dupC | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 47574344 | |||||
| chr6:47574920
|
T | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.729+669T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47574920 | ||||||
| chr6:47574943
|
T | C | 24 | a0001c0001t0006g0179a0001c0001t0006g0180a0001c0001t0006g0183others(21): Show | 24 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.729+692T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47574943 | ||||||
| chr6:47574970
|
G | A | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.729+719G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47574970 | ||||||
| chr6:47575010
|
G | C | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.729+759G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47575010 | ||||||
| chr6:47575128
|
C | T | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.729+877C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47575128 | ||||||
| chr6:47575141
|
A | G | 2 | a0001c0001t0005g0271a0001c0001t0005g0272 | 2 | HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.729+890A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47575141 | ||||||
| chr6:47575207
|
G | A | 1 | a0001c0001t0098g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.729+956G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47575207 | ||||||
| chr6:47575235
|
G | T | 1 | a0001c0001t0042g0192 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.729+984G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47575235 | ||||||
| chr6:47575337
|
T | C | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+1086T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47575337 | ||||||
| chr6:47575650
|
A | T | 1 | a0001c0001t0096g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.730-874A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47575650 | ||||||
| chr6:47575703
|
A | G | 1 | a0001c0001t0042g0192 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.730-821A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47575703 | ||||||
| chr6:47575887
|
T | C | 1 | a0001c0001t0003g0067 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.730-637T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47575887 | ||||||
| chr6:47575934
|
A | C | 1 | a0001c0001t0014g0121 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.730-590A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47575934 | ||||||
| chr6:47575952
|
T | A | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.730-572T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47575952 | ||||||
| chr6:47576161
|
G | C | 78 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(75): Show | 78 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.730-363G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47576161 | ||||||
| chr6:47576322
|
A | G | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-202A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47576322 | ||||||
| chr6:47576418
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.730-106A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47576418 | ||||||
| chr6:47576436
|
A | G | 1 | a0001c0001t0059g0298 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.730-88A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47576436 | ||||||
| chr6:47576458
|
A | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.730-66A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | chr6 | 47576458 | ||||||
| chr6:47576466
|
TA | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-56delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 47576466 | |||||
| chr6:47576651
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.808+49C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 7/17 | chr6 | 47576651 | ||||||
| chr6:47576998
|
C | A | 7 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0071others(4): Show | 7 | NA18942.hp1 NA18946.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.809-11C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 7/17 | chr6 | 47576998 | ||||||
| chr6:47577273
|
A | G | 1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.903+170A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47577273 | ||||||
| chr6:47577274
|
C | T | 2 | a0001c0001t0017g0042a0001c0001t0017g0044 | 2 | NA18954.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.903+171C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47577274 | ||||||
| chr6:47577293
|
C | G | 4 | a0001c0001t0005g0271a0001c0001t0005g0272a0001c0001t0011g0250others(1): Show | 4 | HG01358.hp1 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.903+190C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47577293 | ||||||
| chr6:47577322
|
C | T | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.903+219C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47577322 | ||||||
| chr6:47577512
|
A | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.903+409A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47577512 | ||||||
| chr6:47577668
|
G | C | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.903+565G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47577668 | ||||||
| chr6:47577794
|
T | A | 1 | a0001c0001t0006g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.903+691T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47577794 | ||||||
| chr6:47577956
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.903+853G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47577956 | ||||||
| chr6:47577978
|
G | T | 1 | a0001c0001t0017g0030 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.903+875G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47577978 | ||||||
| chr6:47578032
|
A | T | 1 | a0001c0001t0001g0242 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.903+929A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47578032 | ||||||
| chr6:47578041
|
TTTTG | T | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.903+942_903+945del others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 47578041 | |||||
| chr6:47578195
|
A | G | 5 | a0001c0001t0016g0295a0001c0001t0016g0296a0001c0001t0029g0289others(2): Show | 5 | HG01069.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+1092A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47578195 | ||||||
| chr6:47578276
|
A | G | 2 | a0001c0001t0098g0191a0007c0009t0099g0190 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.904-1109A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47578276 | ||||||
| chr6:47578360
|
C | T | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.904-1025C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47578360 | ||||||
| chr6:47578952
|
C | T | 1 | a0001c0001t0004g0146 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.904-433C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47578952 | ||||||
| chr6:47579020
|
T | G | 7 | a0001c0001t0022g0290a0001c0001t0022g0300a0001c0001t0022g0305others(4): Show | 7 | HG02258.hp1 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-365T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47579020 | ||||||
| chr6:47579182
|
T | C | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.904-203T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47579182 | ||||||
| chr6:47579290
|
G | A | 11 | a0001c0001t0004g0123a0001c0001t0004g0125a0001c0001t0007g0122others(8): Show | 11 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.904-95G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | chr6 | 47579290 | ||||||
| chr6:47579334
|
T | TA | 41 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(38): Show | 41 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.904-37dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 47579334 | |||||
| chr6:47579334
|
T | TAA | 114 | a0001c0001t0002g0092a0001c0001t0003g0017a0001c0001t0003g0053others(111): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.904-38_904-37dupAA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 47579334 | |||||
| chr6:47579334
|
T | TAAA | 149 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(146): Show | 149 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.904-39_904-37dupAA others(1): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 47579334 | |||||
| chr6:47579521
|
T | C | 1 | a0001c0001t0002g0036 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1008+32T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 9/17 | chr6 | 47579521 | ||||||
| chr6:47579763
|
T | C | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1008+274T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 9/17 | chr6 | 47579763 | ||||||
| chr6:47579846
|
T | C | 5 | a0001c0001t0016g0295a0001c0001t0016g0296a0001c0001t0029g0289others(2): Show | 5 | HG01069.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008+357T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 9/17 | chr6 | 47579846 | ||||||
| chr6:47579903
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1008+414C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 9/17 | chr6 | 47579903 | ||||||
| chr6:47579948
|
T | G | 3 | a0001c0001t0001g0242a0001c0001t0001g0248a0001c0001t0001g0252 | 3 | HG00639.hp2 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1008+459T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 9/17 | chr6 | 47579948 | ||||||
| chr6:47580084
|
G | A | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1008+595G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 9/17 | chr6 | 47580084 | ||||||
| chr6:47580411
|
T | C | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1009-453T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 9/17 | chr6 | 47580411 | ||||||
| chr6:47580466
|
CA | C | 261 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(258): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1009-387delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 47580466 | |||||
| chr6:47580564
|
T | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1009-300T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 9/17 | chr6 | 47580564 | ||||||
| chr6:47580587
|
T | C | 2 | a0001c0001t0010g0108a0001c0001t0034g0107 | 2 | HG02683.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1009-277T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 9/17 | chr6 | 47580587 | ||||||
| chr6:47580936
|
C | A | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1045+36C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47580936 | ||||||
| chr6:47581041
|
T | A | 1 | a0001c0001t0012g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1045+141T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47581041 | ||||||
| chr6:47581185
|
A | T | 5 | a0002c0002t0001g0276a0002c0002t0001g0277a0002c0002t0001g0278others(2): Show | 5 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1045+285A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47581185 | ||||||
| chr6:47581206
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1045+306A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47581206 | ||||||
| chr6:47581209
|
G | T | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1045+309G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47581209 | ||||||
| chr6:47581390
|
C | T | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1045+490C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47581390 | ||||||
| chr6:47581610
|
C | G | 1 | a0001c0001t0030g0302 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1046-393C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47581610 | ||||||
| chr6:47581711
|
T | G | 1 | a0001c0001t0049g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1046-292T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47581711 | ||||||
| chr6:47581718
|
A | T | 2 | a0001c0001t0043g0184a0001c0001t0043g0185 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1046-285A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47581718 | ||||||
| chr6:47581759
|
C | T | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1046-244C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47581759 | ||||||
| chr6:47581850
|
A | T | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1046-153A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47581850 | ||||||
| chr6:47581885
|
A | G | 1 | a0001c0001t0042g0192 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1046-118A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47581885 | ||||||
| chr6:47581893
|
A | G | 35 | a0001c0001t0001g0212a0001c0001t0001g0215a0001c0001t0001g0223others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1046-110A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47581893 | ||||||
| chr6:47581902
|
T | C | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1046-101T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 10/17 | chr6 | 47581902 | ||||||
| chr6:47582147
|
T | C | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1108+82T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47582147 | ||||||
| chr6:47582458
|
G | C | 2 | a0001c0001t0017g0004a0001c0001t0019g0003 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1108+393G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47582458 | ||||||
| chr6:47582577
|
A | G | 12 | a0001c0001t0006g0179a0001c0001t0006g0180a0001c0001t0006g0183others(9): Show | 12 | HG01358.hp2 HG02056.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1108+512A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47582577 | ||||||
| chr6:47582789
|
TG | T | 55 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(52): Show | 55 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1108+725delG | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47582789 | ||||||
| chr6:47582790
|
G | T | 1 | a0001c0001t0007g0153 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1108+725G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47582790 | ||||||
| chr6:47582792
|
T | G | 56 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(53): Show | 56 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.1108+727T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47582792 | ||||||
| chr6:47582793
|
TTG | T | 26 | a0001c0001t0016g0291a0001c0001t0016g0292a0001c0001t0016g0295others(23): Show | 26 | HG01069.hp2 HG01891.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1108+730_1108+731d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47582793 | |||||
| chr6:47582795
|
G | GT | 13 | a0001c0001t0001g0232a0001c0001t0001g0243a0001c0001t0001g0269others(10): Show | 13 | HG01074.hp2 HG01261.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1108+743dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47582795 | |||||
| chr6:47582795
|
G | T | 56 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(53): Show | 56 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.1108+730G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47582795 | ||||||
| chr6:47582795
|
GT | G | 93 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(90): Show | 93 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1108+743delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47582795 | |||||
| chr6:47582801
|
T | G | 84 | a0001c0001t0002g0064a0001c0001t0004g0105a0001c0001t0004g0110others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1108+736T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47582801 | ||||||
| chr6:47582945
|
G | A | 1 | a0001c0001t0075g0010 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1108+880G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47582945 | ||||||
| chr6:47583107
|
G | T | 10 | a0001c0001t0001g0208a0001c0001t0001g0234a0001c0001t0001g0235others(7): Show | 10 | NA18943.hp1 NA18950.hp2 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.1108+1042G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47583107 | ||||||
| chr6:47583299
|
G | A | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1108+1234G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47583299 | ||||||
| chr6:47583353
|
T | C | 1 | a0001c0001t0083g0157 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1108+1288T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47583353 | ||||||
| chr6:47583446
|
G | A | 2 | a0001c0001t0086g0015a0001c0001t0089g0050 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1108+1381G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47583446 | ||||||
| chr6:47583680
|
C | T | 1 | a0001c0001t0067g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1108+1615C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47583680 | ||||||
| chr6:47583708
|
T | A | 1 | a0001c0001t0007g0099 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1108+1643T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47583708 | ||||||
| chr6:47583708
|
T | C | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1108+1643T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47583708 | ||||||
| chr6:47583850
|
A | C | 1 | a0001c0001t0089g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1108+1785A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47583850 | ||||||
| chr6:47584001
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1108+1936C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47584001 | ||||||
| chr6:47584125
|
T | C | 84 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1108+2060T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47584125 | ||||||
| chr6:47584202
|
G | A | 84 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1108+2137G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47584202 | ||||||
| chr6:47584338
|
A | T | 1 | a0001c0001t0100g0187 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1108+2273A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47584338 | ||||||
| chr6:47584399
|
T | C | 1 | a0001c0001t0013g0013 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1108+2334T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47584399 | ||||||
| chr6:47584419
|
AT | A | 163 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1108+2369delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47584419 | |||||
| chr6:47584444
|
A | T | 63 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1108+2379A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47584444 | ||||||
| chr6:47584465
|
G | A | 1 | a0001c0001t0051g0287 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1108+2400G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47584465 | ||||||
| chr6:47584552
|
T | A | 1 | a0001c0001t0001g0208 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1108+2487T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47584552 | ||||||
| chr6:47584579
|
G | C | 2 | a0001c0001t0077g0113a0001c0001t0088g0112 | 2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1108+2514G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47584579 | ||||||
| chr6:47584611
|
C | A | 1 | a0001c0001t0041g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1108+2546C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47584611 | ||||||
| chr6:47584877
|
T | C | 1 | a0002c0002t0001g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1108+2812T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47584877 | ||||||
| chr6:47584932
|
G | C | 1 | a0006c0010t0032g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1108+2867G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47584932 | ||||||
| chr6:47584988
|
A | G | 1 | a0001c0001t0020g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1108+2923A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47584988 | ||||||
| chr6:47585016
|
G | A | 91 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(88): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1108+2951G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585016 | ||||||
| chr6:47585081
|
C | A | 84 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1108+3016C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585081 | ||||||
| chr6:47585121
|
G | A | 1 | a0006c0010t0032g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1108+3056G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585121 | ||||||
| chr6:47585140
|
T | TA | 9 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0071others(6): Show | 9 | HG01515.hp1 NA18942.hp1 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.1108+3088dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47585140 | |||||
| chr6:47585184
|
T | A | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1108+3119T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585184 | ||||||
| chr6:47585193
|
C | G | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108+3128C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585193 | ||||||
| chr6:47585198
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1108+3133G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585198 | ||||||
| chr6:47585202
|
C | CT | 78 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(75): Show | 78 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1108+3138dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47585202 | |||||
| chr6:47585252
|
G | T | 1 | a0001c0001t0035g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1108+3187G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585252 | ||||||
| chr6:47585418
|
G | A | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1108+3353G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585418 | ||||||
| chr6:47585432
|
A | G | 2 | a0001c0001t0019g0039a0001c0001t0019g0084 | 2 | NA19000.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1108+3367A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585432 | ||||||
| chr6:47585452
|
C | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108+3387C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585452 | ||||||
| chr6:47585480
|
A | T | 1 | a0001c0001t0070g0009 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1108+3415A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585480 | ||||||
| chr6:47585565
|
C | T | 2 | a0001c0001t0004g0319a0001c0001t0024g0142 | 2 | NA18968.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1108+3500C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585565 | ||||||
| chr6:47585665
|
C | A | 85 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1108+3600C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585665 | ||||||
| chr6:47585666
|
G | A | 62 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1108+3601G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585666 | ||||||
| chr6:47585677
|
T | C | 1 | a0001c0001t0012g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1108+3612T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47585677 | ||||||
| chr6:47585748
|
TG | T | 75 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1108+3685delG | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47585748 | |||||
| chr6:47586158
|
G | A | 85 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1108+4093G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47586158 | ||||||
| chr6:47586276
|
GA | G | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108+4214delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47586276 | |||||
| chr6:47586342
|
A | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1108+4277A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47586342 | ||||||
| chr6:47586419
|
G | C | 1 | a0001c0001t0003g0076 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1108+4354G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47586419 | ||||||
| chr6:47586427
|
T | C | 1 | a0001c0001t0003g0076 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1108+4362T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47586427 | ||||||
| chr6:47586441
|
G | A | 62 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1108+4376G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47586441 | ||||||
| chr6:47586591
|
C | G | 1 | a0001c0001t0018g0014 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1108+4526C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47586591 | ||||||
| chr6:47586669
|
G | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1108+4604G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47586669 | ||||||
| chr6:47586732
|
T | G | 62 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(59): Show | 62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1108+4667T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47586732 | ||||||
| chr6:47586771
|
A | C | 83 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1108+4706A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47586771 | ||||||
| chr6:47586934
|
AT | A | 10 | a0001c0001t0001g0208a0001c0001t0001g0234a0001c0001t0001g0235others(7): Show | 10 | NA18943.hp1 NA18950.hp2 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.1108+4871delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47586934 | |||||
| chr6:47587159
|
A | G | 1 | a0001c0001t0020g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1108+5094A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47587159 | ||||||
| chr6:47587163
|
A | G | 1 | a0001c0001t0014g0120 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1108+5098A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47587163 | ||||||
| chr6:47587314
|
G | T | 1 | a0006c0010t0032g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1108+5249G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47587314 | ||||||
| chr6:47587351
|
C | T | 1 | a0001c0001t0011g0259 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1108+5286C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47587351 | ||||||
| chr6:47587428
|
ACT | A | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1108+5367_1108+536 others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47587428 | |||||
| chr6:47587565
|
A | G | 1 | a0001c0001t0018g0014 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1108+5500A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47587565 | ||||||
| chr6:47587771
|
A | T | 318 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1108+5706A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47587771 | ||||||
| chr6:47587784
|
T | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1108+5719T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47587784 | ||||||
| chr6:47587809
|
A | C | 167 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(164): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1108+5744A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47587809 | ||||||
| chr6:47588138
|
A | G | 1 | a0001c0001t0086g0015 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1108+6073A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47588138 | ||||||
| chr6:47588297
|
G | A | 3 | a0001c0001t0007g0099a0001c0001t0007g0101a0001c0001t0069g0100 | 3 | HG00280.hp2 HG00733.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1108+6232G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47588297 | ||||||
| chr6:47588338
|
T | C | 83 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1108+6273T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47588338 | ||||||
| chr6:47588373
|
C | T | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1108+6308C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47588373 | ||||||
| chr6:47588433
|
T | A | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1108+6368T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47588433 | ||||||
| chr6:47588694
|
C | G | 1 | a0001c0001t0021g0229 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1108+6629C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47588694 | ||||||
| chr6:47588730
|
A | G | 5 | a0001c0001t0016g0295a0001c0001t0016g0296a0001c0001t0029g0289others(2): Show | 5 | HG01069.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108+6665A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47588730 | ||||||
| chr6:47588852
|
T | C | 1 | a0001c0003t0044g0320 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1108+6787T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47588852 | ||||||
| chr6:47588894
|
A | C | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1108+6829A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47588894 | ||||||
| chr6:47588898
|
C | T | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1108+6833C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47588898 | ||||||
| chr6:47588905
|
A | C | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1108+6840A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47588905 | ||||||
| chr6:47588923
|
A | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0266a0001c0001t0049g0282 | 3 | HG01123.hp2 HG01361.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1108+6858A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47588923 | ||||||
| chr6:47588944
|
C | T | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1108+6879C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47588944 | ||||||
| chr6:47589011
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1109-6850A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47589011 | ||||||
| chr6:47589204
|
A | G | 306 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1109-6657A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47589204 | ||||||
| chr6:47589229
|
G | A | 1 | a0001c0001t0030g0302 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1109-6632G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47589229 | ||||||
| chr6:47589341
|
A | G | 2 | a0003c0004t0032g0312a0003c0004t0061g0311 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1109-6520A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47589341 | ||||||
| chr6:47589379
|
T | TACACACA others(5): Show |
38 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(35): Show | 38 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.1109-6478_1109-646 others(16): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589379
|
T | TACACACA others(7): Show |
1 | a0001c0001t0096g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1109-6480_1109-646 others(18): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589379
|
T | TACACACA others(13): Show |
1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1109-6467_1109-646 others(24): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589379
|
T | TACACACA others(19): Show |
1 | a0001c0001t0025g0024 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1109-6467_1109-646 others(30): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589379
|
T | TACACACA others(27): Show |
1 | a0001c0001t0038g0051 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1109-6467_1109-646 others(38): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589379
|
T | TATACACA others(5): Show |
1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1109-6481_1109-648 others(16): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589379
|
T | TATACACA others(11): Show |
2 | a0001c0001t0005g0216a0001c0001t0005g0217 | 2 | NA18953.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1109-6481_1109-648 others(22): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589379
|
T | TATACACA others(13): Show |
10 | a0001c0001t0001g0246a0001c0001t0001g0274a0001c0001t0001g0275others(7): Show | 10 | HG03225.hp2 HG03486.hp1 HG03516.hp1 others(7): Show |
intron_variant | MODIFIER | c.1109-6481_1109-648 others(24): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589379
|
T | TATACACA others(15): Show |
82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1109-6481_1109-648 others(26): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589379
|
T | TATACACA others(17): Show |
14 | a0001c0001t0001g0273a0001c0001t0002g0046a0001c0001t0002g0090others(11): Show | 14 | HG00438.hp1 HG01069.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1109-6481_1109-648 others(28): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589379
|
T | TATACACA others(19): Show |
126 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(123): Show | 126 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1109-6481_1109-648 others(30): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589379
|
T | TATACACA others(21): Show |
19 | a0001c0001t0002g0035a0001c0001t0002g0074a0001c0001t0002g0088others(16): Show | 19 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.1109-6481_1109-648 others(32): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589379
|
T | TATACACA others(23): Show |
3 | a0001c0001t0002g0034a0001c0001t0009g0002a0001c0001t0085g0147 | 3 | HG00140.hp1 HG03453.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1109-6481_1109-648 others(34): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589379
|
T | TATATACA others(19): Show |
3 | a0001c0001t0019g0039a0001c0001t0019g0061a0001c0001t0019g0084 | 3 | NA18975.hp2 NA19000.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1109-6481_1109-648 others(30): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589379 | |||||
| chr6:47589381
|
C | T | 4 | a0001c0001t0003g0063a0001c0001t0083g0157a0001c0001t0090g0154others(1): Show | 4 | HG04199.hp2 NA18969.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109-6480C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47589381 | ||||||
| chr6:47589394
|
A | ACACACAC others(14): Show |
1 | a0001c0001t0003g0063 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1109-6467_1109-646 others(25): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47589394 | ||||||
| chr6:47589394
|
A | ACACACAC others(18): Show |
1 | a0001c0001t0090g0154 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1109-6467_1109-646 others(29): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47589394 | ||||||
| chr6:47589394
|
A | ACACACAC others(20): Show |
1 | a0001c0001t0083g0157 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1109-6467_1109-646 others(31): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47589394 | ||||||
| chr6:47589394
|
A | ACACACAC others(22): Show |
1 | a0001c0001t0094g0148 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1109-6467_1109-646 others(33): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47589394 | ||||||
| chr6:47589436
|
A | G | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1109-6425A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47589436 | ||||||
| chr6:47589534
|
A | ATATG | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1109-6324_1109-632 others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589534 | |||||
| chr6:47589551
|
T | C | 31 | a0001c0001t0002g0035a0001c0001t0007g0152a0001c0001t0007g0153others(28): Show | 31 | HG01069.hp2 HG01255.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.1109-6310T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47589551 | ||||||
| chr6:47589551
|
T | TAC | 93 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(90): Show | 93 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1109-6296_1109-629 others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589551 | |||||
| chr6:47589563
|
C | CAT | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1109-6297_1109-629 others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589563 | |||||
| chr6:47589563
|
C | CATATATA others(11): Show |
2 | a0001c0001t0005g0216a0001c0001t0005g0217 | 2 | NA18953.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1109-6297_1109-629 others(22): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589563 | |||||
| chr6:47589565
|
C | CACACACA others(5): Show |
1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1109-6295_1109-629 others(16): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACACA others(9): Show |
5 | a0001c0001t0016g0295a0001c0001t0016g0296a0001c0001t0029g0289others(2): Show | 5 | HG01069.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(20): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACACA others(11): Show |
1 | a0001c0001t0024g0142 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1109-6295_1109-629 others(22): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACACA others(21): Show |
1 | a0001c0001t0001g0223 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1109-6295_1109-629 others(32): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACACA others(27): Show |
1 | a0001c0001t0028g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1109-6295_1109-629 others(38): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACATA others(3): Show |
2 | a0001c0001t0071g0205a0001c0001t0076g0206 | 2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(14): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACATA others(7): Show |
5 | a0001c0001t0016g0292a0001c0001t0022g0300a0001c0001t0029g0293others(2): Show | 5 | HG02630.hp1 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(18): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACATA others(9): Show |
12 | a0001c0001t0004g0138a0001c0001t0007g0101a0001c0001t0007g0156others(9): Show | 12 | HG01074.hp1 HG01123.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(20): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACATA others(11): Show |
28 | a0001c0001t0004g0114a0001c0001t0004g0132a0001c0001t0004g0146others(25): Show | 28 | HG00140.hp2 HG00558.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(22): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACATA others(13): Show |
14 | a0001c0001t0001g0273a0001c0001t0004g0105a0001c0001t0004g0125others(11): Show | 14 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(11): Show |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(24): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACATA others(15): Show |
12 | a0001c0001t0001g0254a0001c0001t0004g0123a0001c0001t0007g0122others(9): Show | 12 | HG00639.hp1 HG01123.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(26): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACATA others(17): Show |
5 | a0001c0001t0001g0266a0001c0001t0005g0255a0001c0001t0011g0259others(2): Show | 5 | HG01496.hp2 HG02056.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(28): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACATA others(23): Show |
3 | a0001c0001t0004g0136a0001c0001t0004g0139a0001c0001t0057g0288 | 3 | HG00597.hp1 HG02135.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(34): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACATA others(25): Show |
1 | a0001c0001t0004g0110 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1109-6295_1109-629 others(36): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACACATA others(29): Show |
1 | a0001c0001t0028g0210 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1109-6295_1109-629 others(40): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACATATA others(7): Show |
1 | a0002c0002t0001g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1109-6295_1109-629 others(18): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACATATA others(9): Show |
3 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0280 | 3 | HG01243.hp1 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(20): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACATATA others(11): Show |
9 | a0001c0001t0001g0239a0001c0001t0001g0245a0001c0001t0001g0246others(6): Show | 9 | HG01358.hp1 HG01433.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(22): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACATATA others(13): Show |
19 | a0001c0001t0001g0215a0001c0001t0001g0228a0001c0001t0001g0234others(16): Show | 19 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(24): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACATATA others(15): Show |
15 | a0001c0001t0001g0212a0001c0001t0001g0225a0001c0001t0001g0232others(12): Show | 15 | HG00323.hp1 HG00642.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(26): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACATATA others(17): Show |
10 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0267others(7): Show | 10 | HG01261.hp2 HG01361.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(28): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACATATA others(19): Show |
6 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0011g0250others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(30): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACATATA others(21): Show |
2 | a0001c0001t0001g0268a0001c0001t0015g0263 | 2 | NA19006.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(32): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACATATA others(23): Show |
3 | a0001c0001t0001g0257a0001c0001t0054g0211a0001c0001t0055g0098 | 3 | HG01255.hp2 HG02886.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(34): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACATATA others(25): Show |
2 | a0001c0001t0001g0233a0001c0001t0064g0284 | 2 | NA19060.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1109-6295_1109-629 others(36): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CACATATA others(29): Show |
1 | a0001c0001t0001g0247 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1109-6295_1109-629 others(40): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | CATATATA others(19): Show |
1 | a0001c0001t0053g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1109-6280_1109-627 others(30): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47589565 | |||||
| chr6:47589565
|
C | T | 5 | a0001c0001t0005g0216a0001c0001t0005g0217a0003c0004t0032g0312others(2): Show | 5 | HG03225.hp2 HG03486.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.1109-6296C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47589565 | ||||||
| chr6:47589645
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1109-6216A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47589645 | ||||||
| chr6:47590197
|
T | C | 1 | a0001c0001t0084g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1109-5664T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47590197 | ||||||
| chr6:47590249
|
G | T | 75 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1109-5612G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47590249 | ||||||
| chr6:47590302
|
G | A | 1 | a0001c0001t0050g0218 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1109-5559G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47590302 | ||||||
| chr6:47590314
|
A | T | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1109-5547A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47590314 | ||||||
| chr6:47590353
|
C | T | 1 | a0001c0001t0011g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1109-5508C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47590353 | ||||||
| chr6:47590577
|
G | T | 2 | a0001c0001t0043g0184a0001c0001t0043g0185 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1109-5284G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47590577 | ||||||
| chr6:47590713
|
G | A | 1 | a0001c0001t0087g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1109-5148G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47590713 | ||||||
| chr6:47590842
|
A | G | 2 | a0001c0001t0001g0254a0001c0001t0001g0266 | 2 | HG01123.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1109-5019A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47590842 | ||||||
| chr6:47590920
|
G | A | 1 | a0001c0001t0042g0192 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1109-4941G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47590920 | ||||||
| chr6:47591033
|
A | G | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1109-4828A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47591033 | ||||||
| chr6:47591153
|
C | T | 78 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(75): Show | 78 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1109-4708C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47591153 | ||||||
| chr6:47591251
|
A | G | 16 | a0001c0001t0003g0053a0001c0001t0009g0002a0001c0001t0013g0013others(13): Show | 16 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1109-4610A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47591251 | ||||||
| chr6:47591404
|
T | C | 11 | a0001c0001t0003g0053a0001c0001t0009g0002a0001c0001t0013g0013others(8): Show | 11 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1109-4457T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47591404 | ||||||
| chr6:47591656
|
C | T | 2 | a0001c0001t0075g0010a0001c0001t0078g0011 | 2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1109-4205C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47591656 | ||||||
| chr6:47591664
|
G | A | 1 | a0001c0001t0034g0140 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1109-4197G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47591664 | ||||||
| chr6:47591715
|
A | G | 84 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1109-4146A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47591715 | ||||||
| chr6:47591793
|
A | T | 1 | a0001c0001t0095g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1109-4068A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47591793 | ||||||
| chr6:47591808
|
C | T | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1109-4053C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47591808 | ||||||
| chr6:47592205
|
G | T | 39 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(36): Show | 39 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.1109-3656G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47592205 | ||||||
| chr6:47592231
|
A | G | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1109-3630A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47592231 | ||||||
| chr6:47592581
|
G | A | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1109-3280G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47592581 | ||||||
| chr6:47592725
|
A | G | 306 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1109-3136A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47592725 | ||||||
| chr6:47592976
|
C | T | 1 | a0001c0001t0078g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1109-2885C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47592976 | ||||||
| chr6:47593061
|
C | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1109-2800C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47593061 | ||||||
| chr6:47593092
|
T | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1109-2769T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47593092 | ||||||
| chr6:47593271
|
T | C | 2 | a0001c0001t0075g0010a0001c0001t0078g0011 | 2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1109-2590T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47593271 | ||||||
| chr6:47593339
|
C | T | 1 | a0001c0001t0025g0024 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1109-2522C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47593339 | ||||||
| chr6:47593392
|
C | T | 1 | a0001c0001t0028g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1109-2469C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47593392 | ||||||
| chr6:47593445
|
A | G | 2 | a0001c0001t0005g0221a0001c0001t0015g0222 | 2 | NA18988.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1109-2416A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47593445 | ||||||
| chr6:47593806
|
C | T | 1 | a0001c0001t0069g0100 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1109-2055C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47593806 | ||||||
| chr6:47593842
|
T | C | 39 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(36): Show | 39 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.1109-2019T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47593842 | ||||||
| chr6:47593920
|
A | G | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1109-1941A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47593920 | ||||||
| chr6:47594095
|
A | G | 5 | a0001c0001t0001g0213a0001c0001t0001g0239a0001c0001t0001g0249others(2): Show | 5 | HG00323.hp1 HG01109.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1109-1766A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47594095 | ||||||
| chr6:47594551
|
T | A | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1109-1310T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47594551 | ||||||
| chr6:47595030
|
C | T | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1109-831C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47595030 | ||||||
| chr6:47595179
|
A | G | 84 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1109-682A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47595179 | ||||||
| chr6:47595349
|
G | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1109-512G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47595349 | ||||||
| chr6:47595495
|
C | A | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1109-366C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47595495 | ||||||
| chr6:47595680
|
G | A | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1109-181G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47595680 | ||||||
| chr6:47595705
|
TAAA | T | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1109-154_1109-152d others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 47595705 | |||||
| chr6:47595709
|
A | T | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1109-152A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47595709 | ||||||
| chr6:47595711
|
A | T | 4 | a0002c0002t0001g0276a0002c0002t0001g0278a0002c0002t0001g0279others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1109-150A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 11/17 | chr6 | 47595711 | ||||||
| chr6:47596062
|
T | G | 2 | a0001c0001t0004g0138a0001c0001t0014g0133 | 2 | HG01099.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1274+36T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47596062 | ||||||
| chr6:47596468
|
C | T | 96 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1274+442C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47596468 | ||||||
| chr6:47596568
|
C | T | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1274+542C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47596568 | ||||||
| chr6:47596628
|
G | A | 3 | a0001c0001t0002g0081a0001c0001t0002g0096a0001c0001t0013g0091 | 3 | NA18986.hp1 NA19059.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1274+602G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47596628 | ||||||
| chr6:47596851
|
G | A | 1 | a0001c0001t0008g0178 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1274+825G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47596851 | ||||||
| chr6:47596945
|
G | A | 3 | a0001c0001t0006g0167a0001c0001t0008g0310a0001c0001t0042g0168 | 3 | HG01891.hp2 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1274+919G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47596945 | ||||||
| chr6:47596993
|
CATGTTGA others(2174): Show |
C | 2 | a0001c0001t0010g0108a0001c0001t0034g0107 | 2 | HG02683.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1274+969_1275-126d others(2): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 47596993 | |||||
| chr6:47597180
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1274+1154G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47597180 | ||||||
| chr6:47597221
|
G | A | 1 | a0001c0001t0010g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1274+1195G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47597221 | ||||||
| chr6:47597788
|
TGTC | T | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1275-1510_1275-150 others(7): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 47597788 | |||||
| chr6:47597948
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1275-1353C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47597948 | ||||||
| chr6:47598190
|
C | T | 5 | a0001c0001t0075g0010a0001c0001t0078g0011a0003c0004t0032g0312others(2): Show | 5 | HG00642.hp2 HG02257.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1275-1111C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47598190 | ||||||
| chr6:47598225
|
C | T | 3 | a0001c0001t0028g0210a0001c0001t0054g0211a0001c0001t0057g0288 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1275-1076C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47598225 | ||||||
| chr6:47598365
|
A | G | 16 | a0001c0001t0016g0291a0001c0001t0016g0292a0001c0001t0016g0295others(13): Show | 16 | HG01069.hp2 HG01891.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1275-936A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47598365 | ||||||
| chr6:47598371
|
A | G | 1 | a0001c0001t0065g0197 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1275-930A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47598371 | ||||||
| chr6:47598454
|
A | G | 1 | a0001c0001t0051g0287 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1275-847A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47598454 | ||||||
| chr6:47598671
|
C | T | 98 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(95): Show | 98 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1275-630C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47598671 | ||||||
| chr6:47598672
|
G | C | 3 | a0001c0001t0004g0114a0001c0001t0004g0132a0001c0001t0034g0140 | 3 | HG00140.hp2 HG01346.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1275-629G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47598672 | ||||||
| chr6:47598696
|
A | G | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1275-605A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47598696 | ||||||
| chr6:47598935
|
T | A | 3 | a0001c0001t0076g0206a0003c0004t0032g0312a0003c0004t0061g0311 | 3 | HG03453.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1275-366T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47598935 | ||||||
| chr6:47599005
|
C | T | 3 | a0001c0001t0036g0158a0001c0001t0036g0159a0001c0001t0084g0160 | 3 | HG02055.hp2 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1275-296C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47599005 | ||||||
| chr6:47599100
|
C | A | 2 | a0001c0001t0002g0041a0001c0001t0003g0089 | 2 | NA19011.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1275-201C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47599100 | ||||||
| chr6:47599240
|
C | T | 4 | a0001c0001t0023g0198a0001c0001t0023g0202a0001c0001t0023g0203others(1): Show | 4 | HG00741.hp1 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1275-61C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47599240 | ||||||
| chr6:47599281
|
G | A | 12 | a0001c0001t0012g0200a0001c0001t0012g0201a0001c0001t0012g0322others(9): Show | 12 | HG00741.hp1 HG01884.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1275-20G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 12/17 | chr6 | 47599281 | ||||||
| chr6:47599702
|
C | G | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1417+259C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47599702 | ||||||
| chr6:47599975
|
GT | G | 75 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1417+542delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 47599975 | |||||
| chr6:47599976
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1417+533T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47599976 | ||||||
| chr6:47600023
|
C | T | 91 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(88): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1417+580C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47600023 | ||||||
| chr6:47600098
|
G | A | 1 | a0001c0001t0003g0067 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1417+655G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47600098 | ||||||
| chr6:47600179
|
A | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1417+736A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47600179 | ||||||
| chr6:47600418
|
A | G | 1 | a0006c0010t0032g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1417+975A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47600418 | ||||||
| chr6:47600454
|
C | T | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1417+1011C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47600454 | ||||||
| chr6:47600469
|
C | T | 3 | a0001c0001t0020g0175a0001c0001t0020g0176a0001c0001t0020g0177 | 3 | HG00735.hp1 HG01943.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1417+1026C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47600469 | ||||||
| chr6:47600590
|
AT | A | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1417+1150delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 47600590 | |||||
| chr6:47600646
|
G | A | 1 | a0001c0001t0034g0140 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1417+1203G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47600646 | ||||||
| chr6:47600723
|
C | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1417+1280C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47600723 | ||||||
| chr6:47600842
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1417+1399A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47600842 | ||||||
| chr6:47600871
|
A | G | 1 | a0001c0001t0017g0044 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1417+1428A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47600871 | ||||||
| chr6:47600928
|
A | G | 1 | a0001c0001t0006g0186 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1417+1485A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47600928 | ||||||
| chr6:47600960
|
A | G | 81 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(78): Show | 81 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1417+1517A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47600960 | ||||||
| chr6:47601057
|
T | G | 1 | a0001c0001t0015g0264 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1417+1614T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47601057 | ||||||
| chr6:47601086
|
G | A | 3 | a0001c0001t0036g0158a0001c0001t0036g0159a0001c0001t0084g0160 | 3 | HG02055.hp2 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1417+1643G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47601086 | ||||||
| chr6:47601165
|
A | G | 1 | a0001c0001t0005g0260 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1417+1722A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47601165 | ||||||
| chr6:47601241
|
C | T | 1 | a0001c0001t0011g0231 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1417+1798C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47601241 | ||||||
| chr6:47601244
|
T | C | 1 | a0001c0001t0021g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1417+1801T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47601244 | ||||||
| chr6:47601274
|
T | C | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1417+1831T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47601274 | ||||||
| chr6:47601530
|
T | C | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1417+2087T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47601530 | ||||||
| chr6:47601587
|
A | C | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1417+2144A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47601587 | ||||||
| chr6:47601752
|
C | T | 1 | a0001c0001t0009g0022 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1417+2309C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47601752 | ||||||
| chr6:47601771
|
A | C | 1 | a0001c0001t0010g0131 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1417+2328A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47601771 | ||||||
| chr6:47601821
|
A | C | 86 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1417+2378A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47601821 | ||||||
| chr6:47602140
|
G | A | 85 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1417+2697G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47602140 | ||||||
| chr6:47602245
|
A | G | 1 | a0001c0001t0035g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1417+2802A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47602245 | ||||||
| chr6:47602452
|
T | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1417+3009T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47602452 | ||||||
| chr6:47602576
|
G | A | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1417+3133G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47602576 | ||||||
| chr6:47602659
|
G | A | 82 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1417+3216G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47602659 | ||||||
| chr6:47602667
|
G | C | 1 | a0001c0001t0003g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1417+3224G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47602667 | ||||||
| chr6:47602728
|
GA | G | 42 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(39): Show | 42 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.1417+3299delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 47602728 | |||||
| chr6:47602729
|
A | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1417+3286A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47602729 | ||||||
| chr6:47602757
|
T | C | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1417+3314T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47602757 | ||||||
| chr6:47602811
|
G | T | 1 | a0001c0001t0078g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1418-3354G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47602811 | ||||||
| chr6:47602922
|
A | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1418-3243A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47602922 | ||||||
| chr6:47602937
|
A | G | 1 | a0006c0010t0032g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1418-3228A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47602937 | ||||||
| chr6:47602940
|
A | T | 1 | a0001c0001t0001g0249 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1418-3225A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47602940 | ||||||
| chr6:47603353
|
T | C | 83 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1418-2812T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47603353 | ||||||
| chr6:47603479
|
G | A | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1418-2686G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47603479 | ||||||
| chr6:47603522
|
T | C | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1418-2643T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47603522 | ||||||
| chr6:47603641
|
G | A | 5 | a0001c0001t0020g0175a0001c0001t0020g0176a0001c0001t0020g0177others(2): Show | 5 | HG00735.hp1 HG01243.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1418-2524G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47603641 | ||||||
| chr6:47603682
|
T | C | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1418-2483T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47603682 | ||||||
| chr6:47603885
|
T | G | 1 | a0001c0001t0003g0067 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1418-2280T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47603885 | ||||||
| chr6:47603889
|
G | A | 2 | a0001c0001t0010g0108a0001c0001t0034g0107 | 2 | HG02683.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1418-2276G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47603889 | ||||||
| chr6:47604485
|
T | C | 1 | a0001c0001t0034g0107 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1418-1680T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47604485 | ||||||
| chr6:47604493
|
C | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1418-1672C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47604493 | ||||||
| chr6:47604508
|
A | G | 2 | a0001c0001t0062g0163a0001c0001t0063g0164 | 2 | NA18977.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1418-1657A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47604508 | ||||||
| chr6:47604600
|
A | G | 1 | a0001c0001t0076g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1418-1565A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47604600 | ||||||
| chr6:47604638
|
C | T | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1418-1527C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47604638 | ||||||
| chr6:47604750
|
A | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1418-1415A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47604750 | ||||||
| chr6:47604899
|
C | A | 307 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(304): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1418-1266C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47604899 | ||||||
| chr6:47605053
|
G | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1418-1112G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47605053 | ||||||
| chr6:47605136
|
A | G | 1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1418-1029A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47605136 | ||||||
| chr6:47605356
|
A | G | 1 | a0001c0001t0100g0187 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1418-809A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47605356 | ||||||
| chr6:47605667
|
A | G | 7 | a0001c0001t0022g0290a0001c0001t0022g0300a0001c0001t0022g0305others(4): Show | 7 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1418-498A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47605667 | ||||||
| chr6:47605818
|
T | C | 1 | a0001c0001t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1418-347T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47605818 | ||||||
| chr6:47605943
|
C | T | 12 | a0001c0001t0012g0200a0001c0001t0012g0201a0001c0001t0012g0322others(9): Show | 12 | HG00741.hp1 HG01884.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1418-222C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47605943 | ||||||
| chr6:47605976
|
AT | A | 50 | a0001c0001t0001g0212a0001c0001t0001g0215a0001c0001t0001g0223others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1418-178delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 47605976 | |||||
| chr6:47605977
|
T | A | 1 | a0001c0001t0011g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1418-188T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47605977 | ||||||
| chr6:47605985
|
T | G | 1 | a0001c0001t0002g0064 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1418-180T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47605985 | ||||||
| chr6:47606125
|
A | G | 1 | a0001c0001t0078g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1418-40A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 13/17 | chr6 | 47606125 | ||||||
| chr6:47606354
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1530+77C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47606354 | ||||||
| chr6:47606496
|
T | A | 6 | a0001c0001t0001g0228a0001c0001t0001g0242a0001c0001t0001g0248others(3): Show | 6 | HG00639.hp2 HG01169.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1530+219T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47606496 | ||||||
| chr6:47606642
|
GT | G | 97 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(94): Show | 97 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1530+373delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr6 | 47606642 | |||||
| chr6:47606850
|
T | C | 3 | a0001c0001t0028g0210a0001c0001t0054g0211a0001c0001t0057g0288 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1530+573T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47606850 | ||||||
| chr6:47606908
|
T | C | 30 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0225others(27): Show | 30 | HG00323.hp1 HG01109.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1530+631T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47606908 | ||||||
| chr6:47607069
|
C | T | 2 | a0001c0001t0004g0319a0001c0001t0024g0142 | 2 | NA18968.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1530+792C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607069 | ||||||
| chr6:47607127
|
G | GGA | 71 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(68): Show | 71 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1531-800_1531-799i others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607127 | ||||||
| chr6:47607130
|
A | T | 71 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(68): Show | 71 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1531-797A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607130 | ||||||
| chr6:47607131
|
G | C | 71 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(68): Show | 71 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1531-796G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607131 | ||||||
| chr6:47607132
|
G | T | 71 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(68): Show | 71 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1531-795G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607132 | ||||||
| chr6:47607134
|
T | G | 71 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(68): Show | 71 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1531-793T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607134 | ||||||
| chr6:47607135
|
C | T | 71 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(68): Show | 71 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1531-792C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607135 | ||||||
| chr6:47607137
|
C | CCATCCAT others(2): Show |
71 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(68): Show | 71 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1531-790_1531-789i others(11): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607137 | ||||||
| chr6:47607239
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1531-688C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607239 | ||||||
| chr6:47607387
|
C | G | 1 | a0001c0001t0091g0005 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1531-540C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607387 | ||||||
| chr6:47607596
|
T | C | 80 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1531-331T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607596 | ||||||
| chr6:47607661
|
G | A | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1531-266G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607661 | ||||||
| chr6:47607712
|
A | G | 1 | a0001c0001t0028g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1531-215A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607712 | ||||||
| chr6:47607874
|
C | A | 1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1531-53C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607874 | ||||||
| chr6:47607894
|
A | G | 2 | a0001c0001t0002g0006a0001c0001t0009g0002 | 2 | HG00140.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1531-33A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 14/17 | chr6 | 47607894 | ||||||
| chr6:47608036
|
G | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1632+8G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 15/17 | chr6 | 47608036 | ||||||
| chr6:47608117
|
G | T | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1632+89G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 15/17 | chr6 | 47608117 | ||||||
| chr6:47608139
|
A | G | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1632+111A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 15/17 | chr6 | 47608139 | ||||||
| chr6:47608252
|
A | T | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1632+224A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 15/17 | chr6 | 47608252 | ||||||
| chr6:47608365
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1632+337A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 15/17 | chr6 | 47608365 | ||||||
| chr6:47608451
|
C | T | 5 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0062others(2): Show | 5 | HG01109.hp1 HG01496.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.1632+423C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 15/17 | chr6 | 47608451 | ||||||
| chr6:47608577
|
G | T | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1633-546G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 15/17 | chr6 | 47608577 | ||||||
| chr6:47608631
|
T | C | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1633-492T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 15/17 | chr6 | 47608631 | ||||||
| chr6:47608700
|
A | G | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1633-423A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 15/17 | chr6 | 47608700 | ||||||
| chr6:47608739
|
A | G | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1633-384A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 15/17 | chr6 | 47608739 | ||||||
| chr6:47609102
|
A | T | 1 | a0001c0001t0002g0062 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1633-21A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 15/17 | chr6 | 47609102 | ||||||
| chr6:47609328
|
G | A | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1814+24G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609328 | ||||||
| chr6:47609393
|
G | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1814+89G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609393 | ||||||
| chr6:47609401
|
G | C | 1 | a0001c0001t0002g0062 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1814+97G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609401 | ||||||
| chr6:47609479
|
C | G | 1 | a0001c0001t0003g0067 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1814+175C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609479 | ||||||
| chr6:47609490
|
G | A | 1 | a0001c0001t0051g0287 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1814+186G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609490 | ||||||
| chr6:47609513
|
C | CA | 39 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(36): Show | 39 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.1814+227dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47609513 | |||||
| chr6:47609513
|
C | CAA | 6 | a0001c0001t0020g0194a0001c0001t0042g0192a0001c0001t0062g0163others(3): Show | 6 | HG03471.hp1 HG03710.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1814+226_1814+227d others(4): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47609513 | |||||
| chr6:47609513
|
C | CAAA | 69 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(66): Show | 69 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1814+225_1814+227d others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47609513 | |||||
| chr6:47609513
|
C | CAAAA | 7 | a0001c0001t0001g0232a0001c0001t0001g0243a0001c0001t0001g0254others(4): Show | 7 | HG01074.hp2 HG01123.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1814+224_1814+227d others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47609513 | |||||
| chr6:47609513
|
CA | C | 86 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(83): Show | 86 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1814+227delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47609513 | |||||
| chr6:47609513
|
CAAA | C | 78 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(75): Show | 78 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1814+225_1814+227d others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47609513 | |||||
| chr6:47609531
|
AG | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0057g0288others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1814+228delG | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609531 | ||||||
| chr6:47609532
|
G | A | 3 | a0001c0001t0053g0097a0001c0001t0054g0211a0001c0001t0055g0098 | 3 | HG01255.hp2 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1814+228G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609532 | ||||||
| chr6:47609535
|
A | G | 93 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(90): Show | 93 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1814+231A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609535 | ||||||
| chr6:47609563
|
G | T | 1 | a0001c0001t0041g0171 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1814+259G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609563 | ||||||
| chr6:47609610
|
G | A | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1814+306G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609610 | ||||||
| chr6:47609647
|
C | T | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1814+343C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609647 | ||||||
| chr6:47609787
|
G | T | 3 | a0001c0001t0036g0158a0001c0001t0036g0159a0001c0001t0084g0160 | 3 | HG02055.hp2 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1814+483G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609787 | ||||||
| chr6:47609916
|
T | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0234a0001c0001t0001g0235others(7): Show | 10 | NA18943.hp1 NA18950.hp2 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.1814+612T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609916 | ||||||
| chr6:47609964
|
C | T | 1 | a0001c0001t0033g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1814+660C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47609964 | ||||||
| chr6:47610112
|
A | G | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1814+808A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610112 | ||||||
| chr6:47610220
|
A | G | 1 | a0001c0001t0010g0150 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1814+916A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610220 | ||||||
| chr6:47610408
|
G | A | 4 | a0001c0001t0005g0271a0001c0001t0005g0272a0001c0001t0011g0250others(1): Show | 4 | HG01358.hp1 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1814+1104G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610408 | ||||||
| chr6:47610435
|
A | G | 1 | a0001c0001t0002g0096 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1814+1131A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610435 | ||||||
| chr6:47610579
|
G | C | 1 | a0001c0001t0056g0299 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1814+1275G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610579 | ||||||
| chr6:47610602
|
G | T | 2 | a0001c0001t0052g0301a0001c0001t0056g0299 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1814+1298G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610602 | ||||||
| chr6:47610949
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1815-1514_1815-150 others(14): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610949 | |||||
| chr6:47610949
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0007g0101 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1815-1516_1815-150 others(16): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610949 | |||||
| chr6:47610949
|
T | TTATATAT others(7): Show |
2 | a0001c0001t0004g0146a0001c0001t0007g0099 | 2 | HG00558.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.1815-1518_1815-150 others(18): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610949 | |||||
| chr6:47610949
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0027g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1815-1520_1815-150 others(20): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610949 | |||||
| chr6:47610949
|
T | TTATATAT others(13): Show |
2 | a0001c0001t0010g0108a0001c0001t0024g0115 | 2 | HG01257.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1815-1505_1815-150 others(24): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610949 | |||||
| chr6:47610949
|
T | TTATATAT others(17): Show |
1 | a0001c0001t0036g0158 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1815-1505_1815-150 others(28): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610949 | |||||
| chr6:47610949
|
T | TTATATAT others(19): Show |
1 | a0001c0001t0037g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1815-1505_1815-150 others(30): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610949 | |||||
| chr6:47610949
|
T | TTATATGT others(7): Show |
1 | a0001c0001t0016g0291 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1815-1519_1815-151 others(18): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610949 | |||||
| chr6:47610949
|
T | TTTTATAT others(13): Show |
1 | a0001c0001t0031g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1815-1523_1815-152 others(24): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610949 | |||||
| chr6:47610949
|
TTA | T | 100 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1815-1506_1815-150 others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610949 | |||||
| chr6:47610967
|
A | G | 1 | a0006c0010t0032g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1815-1506A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610967 | ||||||
| chr6:47610969
|
G | A | 204 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1815-1504G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610969 | ||||||
| chr6:47610971
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0004g0105 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(15): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(8): Show |
4 | a0001c0001t0010g0131a0001c0001t0014g0133a0001c0001t0024g0149others(1): Show | 4 | HG01099.hp2 HG02602.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(19): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0039g0134a0001c0001t0039g0135 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(21): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0082g0145 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(23): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(14): Show |
3 | a0001c0001t0007g0156a0001c0001t0014g0151a0001c0001t0036g0159 | 3 | HG03139.hp1 NA18981.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(25): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0022g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(27): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0022g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(37): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0035g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(34): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0079g0104 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(30): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(20): Show |
2 | a0001c0001t0022g0290a0001c0001t0030g0302 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(31): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0087g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(29): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0029g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(32): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0030g0304a0001c0001t0060g0294 | 2 | HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(27): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0052g0301 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(28): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0016g0295 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(31): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0010g0144 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(24): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0029g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(25): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0016g0292 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(23): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0071g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(25): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0056g0299 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(22): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0016g0296a0001c0001t0031g0297 | 2 | HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(27): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0034g0140 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(18): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0138 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(19): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0059g0298 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(27): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | ATATATAT others(6): Show |
3 | a0001c0001t0004g0110a0001c0001t0004g0136a0001c0001t0004g0139 | 3 | HG00597.hp1 HG02135.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(17): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
A | G | 36 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(33): Show | 36 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1815-1502A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610971 | ||||||
| chr6:47610971
|
AT | A | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1815-1487delT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610971
|
ATT | A | 12 | a0001c0001t0002g0037a0001c0001t0002g0038a0001c0001t0002g0096others(9): Show | 12 | HG00741.hp1 HG01346.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1815-1488_1815-148 others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47610971 | |||||
| chr6:47610972
|
T | TA | 36 | a0001c0001t0006g0167a0001c0001t0006g0179a0001c0001t0006g0180others(33): Show | 36 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(5): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610972 | ||||||
| chr6:47610972
|
T | TATATATA others(4): Show |
1 | a0001c0001t0010g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(15): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610972 | ||||||
| chr6:47610972
|
T | TATATATA others(6): Show |
2 | a0001c0001t0058g0130a0001c0001t0088g0112 | 2 | HG01884.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(17): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610972 | ||||||
| chr6:47610972
|
T | TATATATA others(8): Show |
14 | a0001c0001t0004g0114a0001c0001t0004g0123a0001c0001t0004g0125others(11): Show | 14 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(19): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610972 | ||||||
| chr6:47610972
|
T | TATATATA others(10): Show |
7 | a0001c0001t0004g0129a0001c0001t0007g0137a0001c0001t0027g0119others(4): Show | 7 | HG01192.hp1 HG01515.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(21): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610972 | ||||||
| chr6:47610972
|
T | TATATATA others(12): Show |
5 | a0001c0001t0007g0155a0001c0001t0014g0141a0001c0001t0090g0154others(2): Show | 5 | HG00438.hp2 HG02647.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(23): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610972 | ||||||
| chr6:47610972
|
T | TATATATA others(14): Show |
3 | a0001c0001t0007g0152a0001c0001t0007g0153a0001c0001t0010g0150 | 3 | HG03831.hp1 NA18955.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(25): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610972 | ||||||
| chr6:47610972
|
T | TATATATA others(16): Show |
2 | a0001c0001t0083g0157a0001c0001t0085g0147 | 2 | HG03453.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(27): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610972 | ||||||
| chr6:47610972
|
T | TATATATA others(18): Show |
1 | a0001c0001t0084g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1815-1501_1815-150 others(29): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610972 | ||||||
| chr6:47610972
|
T | TGTA | 3 | a0001c0001t0043g0184a0001c0001t0043g0185a0007c0009t0099g0190 | 3 | HG01168.hp1 HG01169.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1815-1501_1815-150 others(7): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610972 | ||||||
| chr6:47610973
|
T | A | 13 | a0001c0001t0005g0271a0001c0001t0005g0272a0001c0001t0007g0099others(10): Show | 13 | HG00733.hp1 HG01358.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1815-1500T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610973 | ||||||
| chr6:47610974
|
T | A | 8 | a0001c0001t0004g0114a0001c0001t0004g0123a0001c0001t0004g0125others(5): Show | 8 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(5): Show |
intron_variant | MODIFIER | c.1815-1499T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610974 | ||||||
| chr6:47610975
|
T | A | 3 | a0001c0001t0028g0210a0001c0001t0054g0211a0001c0001t0057g0288 | 3 | HG02630.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1815-1498T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610975 | ||||||
| chr6:47610976
|
T | A | 1 | a0001c0001t0004g0114 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1815-1497T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610976 | ||||||
| chr6:47610986
|
TG | T | 9 | a0001c0001t0001g0232a0001c0001t0001g0243a0001c0001t0001g0254others(6): Show | 9 | HG01074.hp2 HG01123.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1815-1486delG | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610986 | ||||||
| chr6:47610987
|
G | T | 70 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(67): Show | 70 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1815-1486G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47610987 | ||||||
| chr6:47611003
|
G | A | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1815-1470G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47611003 | ||||||
| chr6:47611238
|
C | T | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1815-1235C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47611238 | ||||||
| chr6:47611284
|
C | G | 1 | a0001c0001t0096g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1815-1189C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47611284 | ||||||
| chr6:47611381
|
G | C | 1 | a0001c0001t0066g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1815-1092G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47611381 | ||||||
| chr6:47611387
|
G | GA | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1815-1084dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 47611387 | |||||
| chr6:47611410
|
C | T | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1815-1063C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47611410 | ||||||
| chr6:47611475
|
G | A | 1 | a0001c0001t0075g0010 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1815-998G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47611475 | ||||||
| chr6:47611814
|
G | T | 1 | a0001c0001t0011g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1815-659G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47611814 | ||||||
| chr6:47611940
|
T | C | 12 | a0001c0001t0012g0200a0001c0001t0012g0201a0001c0001t0012g0322others(9): Show | 12 | HG00741.hp1 HG01884.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1815-533T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47611940 | ||||||
| chr6:47612164
|
C | T | 1 | a0001c0001t0070g0009 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1815-309C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47612164 | ||||||
| chr6:47612206
|
A | C | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1815-267A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 16/17 | chr6 | 47612206 | ||||||
| chr6:47612613
|
G | A | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1878+77G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47612613 | ||||||
| chr6:47612645
|
G | T | 1 | a0001c0001t0013g0059 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1878+109G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47612645 | ||||||
| chr6:47612670
|
T | TA | 4 | a0001c0001t0022g0290a0001c0001t0022g0300a0001c0001t0052g0301others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1878+135dupA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47612670 | |||||
| chr6:47612808
|
G | A | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1878+272G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47612808 | ||||||
| chr6:47612918
|
C | A | 1 | a0001c0001t0010g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1878+382C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47612918 | ||||||
| chr6:47612919
|
T | C | 1 | a0001c0001t0010g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1878+383T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47612919 | ||||||
| chr6:47612921
|
A | G | 79 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1878+385A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47612921 | ||||||
| chr6:47612922
|
A | G | 1 | a0001c0001t0010g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1878+386A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47612922 | ||||||
| chr6:47612924
|
C | T | 1 | a0001c0001t0010g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1878+388C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47612924 | ||||||
| chr6:47612930
|
C | G | 1 | a0001c0001t0010g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1878+394C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47612930 | ||||||
| chr6:47612932
|
C | G | 1 | a0001c0001t0010g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1878+396C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47612932 | ||||||
| chr6:47612934
|
G | T | 1 | a0001c0001t0010g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1878+398G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47612934 | ||||||
| chr6:47612959
|
G | A | 80 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1878+423G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47612959 | ||||||
| chr6:47613378
|
A | G | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1878+842A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47613378 | ||||||
| chr6:47613407
|
T | A | 1 | a0001c0001t0018g0055 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1878+871T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47613407 | ||||||
| chr6:47613508
|
C | CT | 85 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1878+984dupT | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47613508 | |||||
| chr6:47613586
|
T | C | 79 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(76): Show | 79 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1878+1050T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47613586 | ||||||
| chr6:47613651
|
G | A | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1878+1115G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47613651 | ||||||
| chr6:47613770
|
C | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1878+1234C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47613770 | ||||||
| chr6:47613856
|
C | T | 3 | a0001c0001t0036g0158a0001c0001t0036g0159a0001c0001t0084g0160 | 3 | HG02055.hp2 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1878+1320C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47613856 | ||||||
| chr6:47613942
|
T | G | 1 | a0001c0001t0078g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1878+1406T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47613942 | ||||||
| chr6:47614021
|
G | T | 2 | a0001c0001t0017g0042a0001c0001t0017g0044 | 2 | NA18954.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1878+1485G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47614021 | ||||||
| chr6:47614100
|
A | G | 1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1878+1564A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47614100 | ||||||
| chr6:47614105
|
A | G | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1878+1569A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47614105 | ||||||
| chr6:47614124
|
T | C | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1878+1588T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47614124 | ||||||
| chr6:47614247
|
C | T | 1 | a0001c0001t0075g0010 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1878+1711C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47614247 | ||||||
| chr6:47614408
|
T | G | 6 | a0002c0002t0001g0276a0002c0002t0001g0277a0002c0002t0001g0278others(3): Show | 6 | HG01243.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1878+1872T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47614408 | ||||||
| chr6:47614640
|
G | A | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1878+2104G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47614640 | ||||||
| chr6:47614681
|
A | G | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1878+2145A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47614681 | ||||||
| chr6:47614699
|
A | G | 3 | a0001c0001t0002g0081a0001c0001t0002g0096a0001c0001t0013g0091 | 3 | NA18986.hp1 NA19059.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1878+2163A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47614699 | ||||||
| chr6:47614788
|
C | G | 17 | a0001c0001t0016g0291a0001c0001t0016g0292a0001c0001t0016g0295others(14): Show | 17 | HG01069.hp2 HG01891.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1878+2252C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47614788 | ||||||
| chr6:47614928
|
C | A | 1 | a0001c0001t0017g0042 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1878+2392C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47614928 | ||||||
| chr6:47615010
|
C | T | 1 | a0001c0001t0002g0040 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1878+2474C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615010 | ||||||
| chr6:47615074
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1878+2538C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615074 | ||||||
| chr6:47615505
|
G | A | 1 | a0001c0001t0067g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1878+2969G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615505 | ||||||
| chr6:47615629
|
T | C | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1878+3093T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615629 | ||||||
| chr6:47615709
|
G | A | 1 | a0001c0001t0067g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1878+3173G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615709 | ||||||
| chr6:47615726
|
G | T | 1 | a0001c0001t0051g0287 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1878+3190G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615726 | ||||||
| chr6:47615778
|
TTTTAA | T | 11 | a0001c0001t0001g0243a0001c0001t0005g0216a0001c0001t0005g0217others(8): Show | 11 | HG01074.hp2 HG03927.hp1 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1878+3257_1878+326 others(9): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47615778 | |||||
| chr6:47615782
|
A | T | 306 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1878+3246A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615782 | ||||||
| chr6:47615787
|
A | T | 11 | a0001c0001t0001g0243a0001c0001t0005g0216a0001c0001t0005g0217others(8): Show | 11 | HG01074.hp2 HG03927.hp1 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1878+3251A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615787 | ||||||
| chr6:47615789
|
T | TTTAA | 8 | a0001c0001t0027g0119a0001c0001t0028g0210a0001c0001t0067g0196others(5): Show | 8 | HG01981.hp1 HG02257.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1878+3256_1878+325 others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47615789 | |||||
| chr6:47615789
|
T | TTTAATTA others(5): Show |
1 | a0001c0001t0075g0010 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1878+3259_1878+326 others(16): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47615789 | |||||
| chr6:47615789
|
T | TTTTATTT others(9): Show |
1 | a0001c0001t0003g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1878+3255_1878+325 others(20): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47615789 | |||||
| chr6:47615791
|
TA | T | 51 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0223others(48): Show | 51 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1878+3257delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47615791 | |||||
| chr6:47615792
|
A | AATTT | 65 | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0019others(62): Show | 65 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.1878+3292_1878+329 others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47615792 | |||||
| chr6:47615792
|
A | AATTTATT others(1): Show |
72 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0023others(69): Show | 72 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1878+3288_1878+329 others(12): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47615792 | |||||
| chr6:47615792
|
A | AATTTATT others(5): Show |
2 | a0001c0001t0002g0096a0001c0001t0026g0016 | 2 | HG01168.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.1878+3284_1878+329 others(16): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47615792 | |||||
| chr6:47615792
|
A | ATTT | 11 | a0001c0001t0001g0213a0001c0001t0001g0226a0001c0001t0001g0227others(8): Show | 11 | HG00323.hp1 HG01109.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.1878+3256_1878+325 others(7): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615792 | ||||||
| chr6:47615792
|
A | ATTTATTT | 3 | a0001c0001t0001g0225a0001c0001t0018g0014a0001c0001t0051g0287 | 3 | HG00438.hp1 HG04228.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1878+3256_1878+325 others(11): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615792 | ||||||
| chr6:47615792
|
A | T | 1 | a0001c0001t0003g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1878+3256A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615792 | ||||||
| chr6:47615792
|
AATTT | A | 33 | a0001c0001t0006g0179a0001c0001t0006g0180a0001c0001t0006g0183others(30): Show | 33 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1878+3292_1878+329 others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47615792 | |||||
| chr6:47615792
|
AATTTATT others(5): Show |
A | 3 | a0001c0001t0004g0138a0001c0001t0053g0097a0001c0001t0055g0098 | 3 | HG01123.hp1 HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1878+3284_1878+329 others(16): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47615792 | |||||
| chr6:47615796
|
T | A | 12 | a0001c0001t0004g0110a0001c0001t0004g0136a0001c0001t0004g0139others(9): Show | 12 | HG00597.hp1 HG02135.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1878+3260T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615796 | ||||||
| chr6:47615800
|
T | A | 8 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(5): Show | 8 | HG02257.hp2 HG02602.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1878+3264T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615800 | ||||||
| chr6:47615804
|
T | A | 5 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(2): Show | 5 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1878+3268T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615804 | ||||||
| chr6:47615808
|
T | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1878+3272T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615808 | ||||||
| chr6:47615812
|
T | A | 1 | a0001c0001t0028g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1878+3276T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615812 | ||||||
| chr6:47615816
|
T | A | 1 | a0001c0001t0028g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1878+3280T>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615816 | ||||||
| chr6:47615843
|
G | A | 1 | a0001c0001t0080g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1878+3307G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615843 | ||||||
| chr6:47615925
|
G | A | 2 | a0001c0001t0012g0201a0001c0001t0066g0199 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1878+3389G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615925 | ||||||
| chr6:47615928
|
C | T | 52 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(49): Show | 52 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1878+3392C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615928 | ||||||
| chr6:47615975
|
G | C | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1878+3439G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47615975 | ||||||
| chr6:47616018
|
T | C | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1878+3482T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47616018 | ||||||
| chr6:47616029
|
C | T | 83 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1878+3493C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47616029 | ||||||
| chr6:47616082
|
C | CTT | 32 | a0001c0001t0006g0167a0001c0001t0006g0180a0001c0001t0006g0186others(29): Show | 32 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.1878+3572_1878+357 others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
C | CTTT | 6 | a0001c0001t0006g0179a0001c0001t0006g0183a0001c0001t0006g0316others(3): Show | 6 | HG01358.hp2 HG02602.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1878+3571_1878+357 others(7): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
C | CTTTTT | 8 | a0001c0001t0014g0151a0001c0001t0016g0295a0001c0001t0016g0296others(5): Show | 8 | HG01069.hp2 HG02280.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1878+3569_1878+357 others(9): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
C | CTTTTTT | 10 | a0001c0001t0007g0155a0001c0001t0007g0156a0001c0001t0016g0292others(7): Show | 10 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1878+3568_1878+357 others(10): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
C | CTTTTTTT | 12 | a0001c0001t0007g0137a0001c0001t0007g0152a0001c0001t0007g0153others(9): Show | 12 | HG00280.hp2 HG01192.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1878+3567_1878+357 others(11): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
C | CTTTTTTT others(1): Show |
12 | a0001c0001t0004g0129a0001c0001t0004g0132a0001c0001t0007g0099others(9): Show | 12 | HG00733.hp1 HG01346.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.1878+3566_1878+357 others(12): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
C | CTTTTTTT others(2): Show |
10 | a0001c0001t0004g0105a0001c0001t0004g0114a0001c0001t0004g0123others(7): Show | 10 | HG00140.hp2 HG00639.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1878+3565_1878+357 others(13): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
C | CTTTTTTT others(3): Show |
9 | a0001c0001t0004g0136a0001c0001t0004g0138a0001c0001t0010g0131others(6): Show | 9 | HG01123.hp1 HG01516.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1878+3564_1878+357 others(14): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
C | CTTTTTTT others(4): Show |
20 | a0001c0001t0004g0110a0001c0001t0004g0125a0001c0001t0004g0139others(17): Show | 20 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(17): Show |
intron_variant | MODIFIER | c.1878+3563_1878+357 others(15): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0046g0118a0001c0001t0048g0321a0001c0001t0065g0197 | 3 | HG02148.hp1 HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1878+3562_1878+357 others(16): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0012g0201a0001c0001t0012g0322a0001c0001t0027g0126others(1): Show | 4 | HG02818.hp1 HG03209.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1878+3561_1878+357 others(17): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
CTTTTT | C | 10 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0267others(7): Show | 10 | HG00642.hp1 HG02258.hp2 HG04228.hp1 others(7): Show |
intron_variant | MODIFIER | c.1878+3569_1878+357 others(9): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
CTTTTTT | C | 73 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0223others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1878+3568_1878+357 others(10): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
CTTTTTTT others(3): Show |
C | 9 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0062others(6): Show | 9 | HG01071.hp1 HG01109.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1878+3564_1878+357 others(14): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
CTTTTTTT others(4): Show |
C | 89 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(86): Show | 89 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1878+3563_1878+357 others(15): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616082
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0009g0020 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1878+3562_1878+357 others(16): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47616082 | |||||
| chr6:47616154
|
C | T | 1 | a0001c0001t0030g0302 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1878+3618C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47616154 | ||||||
| chr6:47616183
|
C | T | 1 | a0006c0010t0032g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1878+3647C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47616183 | ||||||
| chr6:47616216
|
C | T | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1878+3680C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47616216 | ||||||
| chr6:47616355
|
G | A | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1878+3819G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47616355 | ||||||
| chr6:47616380
|
C | T | 1 | a0001c0001t0038g0054 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1878+3844C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47616380 | ||||||
| chr6:47616400
|
A | T | 2 | a0001c0001t0005g0255a0005c0007t0005g0224 | 2 | NA18999.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1878+3864A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47616400 | ||||||
| chr6:47616862
|
T | G | 1 | a0001c0001t0022g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1878+4326T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47616862 | ||||||
| chr6:47617032
|
A | G | 98 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(95): Show | 98 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1878+4496A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47617032 | ||||||
| chr6:47617183
|
T | C | 1 | a0001c0001t0074g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1878+4647T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47617183 | ||||||
| chr6:47617193
|
G | A | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1878+4657G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47617193 | ||||||
| chr6:47617370
|
A | T | 80 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1878+4834A>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47617370 | ||||||
| chr6:47617619
|
C | T | 318 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1878+5083C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47617619 | ||||||
| chr6:47617735
|
GA | G | 79 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(76): Show | 79 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1878+5200delA | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47617735 | ||||||
| chr6:47617879
|
A | G | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1878+5343A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47617879 | ||||||
| chr6:47617945
|
A | C | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1878+5409A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47617945 | ||||||
| chr6:47618070
|
G | C | 1 | a0001c0001t0001g0266 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1878+5534G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47618070 | ||||||
| chr6:47618176
|
T | C | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1878+5640T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47618176 | ||||||
| chr6:47618224
|
G | A | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1878+5688G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47618224 | ||||||
| chr6:47618239
|
G | C | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1878+5703G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47618239 | ||||||
| chr6:47618762
|
T | C | 1 | a0001c0001t0097g0181 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1879-5424T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47618762 | ||||||
| chr6:47618773
|
G | A | 1 | a0001c0001t0003g0076 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1879-5413G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47618773 | ||||||
| chr6:47618821
|
G | A | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1879-5365G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47618821 | ||||||
| chr6:47618890
|
T | C | 2 | a0001c0001t0075g0010a0001c0001t0078g0011 | 2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1879-5296T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47618890 | ||||||
| chr6:47619210
|
C | T | 318 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1879-4976C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47619210 | ||||||
| chr6:47619313
|
AACAT | A | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1879-4869_1879-486 others(8): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47619313 | |||||
| chr6:47619372
|
T | G | 1 | a0001c0001t0075g0010 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1879-4814T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47619372 | ||||||
| chr6:47619379
|
A | G | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1879-4807A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47619379 | ||||||
| chr6:47619406
|
T | G | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1879-4780T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47619406 | ||||||
| chr6:47619460
|
G | T | 261 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(258): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1879-4726G>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47619460 | ||||||
| chr6:47619555
|
A | G | 1 | a0001c0005t0068g0001 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1879-4631A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47619555 | ||||||
| chr6:47619558
|
ACTT | A | 80 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1879-4624_1879-462 others(7): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47619558 | |||||
| chr6:47619588
|
G | C | 1 | a0001c0001t0013g0047 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1879-4598G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47619588 | ||||||
| chr6:47620040
|
C | A | 1 | a0001c0001t0007g0153 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1879-4146C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47620040 | ||||||
| chr6:47620080
|
T | G | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1879-4106T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47620080 | ||||||
| chr6:47620288
|
A | G | 3 | a0001c0001t0004g0110a0001c0001t0004g0136a0001c0001t0004g0139 | 3 | HG00597.hp1 HG02135.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1879-3898A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47620288 | ||||||
| chr6:47620486
|
C | T | 1 | a0001c0001t0041g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1879-3700C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47620486 | ||||||
| chr6:47620527
|
C | T | 1 | a0001c0001t0017g0044 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1879-3659C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47620527 | ||||||
| chr6:47620697
|
A | C | 1 | a0001c0001t0064g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1879-3489A>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47620697 | ||||||
| chr6:47620741
|
C | T | 1 | a0001c0001t0016g0296 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1879-3445C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47620741 | ||||||
| chr6:47620750
|
G | A | 1 | a0001c0001t0002g0086 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1879-3436G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47620750 | ||||||
| chr6:47620834
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1879-3352A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47620834 | ||||||
| chr6:47621078
|
A | G | 3 | a0001c0001t0006g0167a0001c0001t0008g0310a0001c0001t0042g0168 | 3 | HG01891.hp2 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1879-3108A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47621078 | ||||||
| chr6:47621211
|
A | G | 1 | a0001c0001t0003g0067 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1879-2975A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47621211 | ||||||
| chr6:47621415
|
C | G | 1 | a0001c0001t0001g0237 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1879-2771C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47621415 | ||||||
| chr6:47621428
|
T | C | 97 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(94): Show | 97 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1879-2758T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47621428 | ||||||
| chr6:47621649
|
T | C | 1 | a0001c0001t0024g0142 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1879-2537T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47621649 | ||||||
| chr6:47621769
|
AG | A | 3 | a0003c0004t0032g0312a0003c0004t0061g0311a0006c0010t0032g0313 | 3 | HG03225.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1879-2415delG | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47621769 | |||||
| chr6:47621897
|
G | A | 83 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1879-2289G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47621897 | ||||||
| chr6:47621910
|
G | A | 1 | a0001c0001t0004g0105 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1879-2276G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47621910 | ||||||
| chr6:47622094
|
G | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1879-2092G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622094 | ||||||
| chr6:47622095
|
C | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1879-2091C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622095 | ||||||
| chr6:47622201
|
C | G | 1 | a0001c0001t0011g0250 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1879-1985C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622201 | ||||||
| chr6:47622337
|
C | A | 1 | a0001c0001t0063g0164 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1879-1849C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622337 | ||||||
| chr6:47622368
|
C | T | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1879-1818C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622368 | ||||||
| chr6:47622426
|
C | G | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1879-1760C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622426 | ||||||
| chr6:47622448
|
CTA | C | 83 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1879-1736_1879-173 others(6): Show |
CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 47622448 | |||||
| chr6:47622463
|
G | A | 2 | a0001c0001t0077g0113a0001c0001t0088g0112 | 2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1879-1723G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622463 | ||||||
| chr6:47622621
|
G | A | 1 | a0001c0001t0060g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1879-1565G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622621 | ||||||
| chr6:47622725
|
C | G | 1 | a0001c0001t0002g0087 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1879-1461C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622725 | ||||||
| chr6:47622740
|
C | T | 83 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0114others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1879-1446C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622740 | ||||||
| chr6:47622756
|
G | A | 1 | a0001c0001t0092g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1879-1430G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622756 | ||||||
| chr6:47622831
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0045g0214 | 2 | HG00323.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1879-1355G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622831 | ||||||
| chr6:47622927
|
T | G | 1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1879-1259T>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622927 | ||||||
| chr6:47622950
|
C | G | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1879-1236C>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47622950 | ||||||
| chr6:47623050
|
C | T | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1879-1136C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47623050 | ||||||
| chr6:47623329
|
G | A | 4 | a0001c0001t0028g0209a0001c0001t0028g0210a0001c0001t0054g0211others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1879-857G>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47623329 | ||||||
| chr6:47623442
|
C | A | 95 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1879-744C>A | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47623442 | ||||||
| chr6:47623471
|
G | C | 67 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(64): Show | 67 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1879-715G>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47623471 | ||||||
| chr6:47623579
|
C | T | 267 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(264): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1879-607C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47623579 | ||||||
| chr6:47623669
|
C | T | 166 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1879-517C>T | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47623669 | ||||||
| chr6:47623936
|
A | G | 2 | a0001c0001t0053g0097a0001c0001t0055g0098 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1879-250A>G | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47623936 | ||||||
| chr6:47624120
|
T | C | 76 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0213others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1879-66T>C | CD2AP | ENSG00000198087.7 | transcript | ENST00000359314.5 | protein_coding | 17/17 | chr6 | 47624120 |