Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11200 |
| ensemblid | ENSG00000183765.24 |
| hgncid | 16627 |
| symbol | CHEK2 |
| name | checkpoint kinase 2 |
| refseq_nuc | NM_007194.4 |
| refseq_prot | NP_009125.1 |
| ensembl_nuc | ENST00000404276.6 |
| ensembl_prot | ENSP00000385747.1 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 28687743 |
| end | 28741820 |
| strand | - |
| ver | v1.2 |
| region | chr22:28687743-28741820 |
| region5000 | chr22:28682743-28746820 |
| regionname0 | CHEK2_chr22_28687743_28741820 |
| regionname5000 | CHEK2_chr22_28682743_28746820 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 543 | 377 | 85 | 67 | 166 | 15 | 42 | 121 | CHEK2_chr22_28682743_28746820 | CHEK2 | MSRES others(538): Show |
chr22 | 28682743 | 28746820 |
| a0002 | 0/0 | 543 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | MSRES others(538): Show |
chr22 | 28682743 | 28746820 |
| a0003 | 0/0 | 543 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | MSRES others(538): Show |
chr22 | 28682743 | 28746820 |
| a0004 | 0/0 | 543 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | MSRES others(538): Show |
chr22 | 28682743 | 28746820 |
| a0005 | 0/0 | 543 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | MSRES others(538): Show |
chr22 | 28682743 | 28746820 |
| a0006 | 0/0 | 543 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | MSRES others(538): Show |
chr22 | 28682743 | 28746820 |
| a0007 | 0/0 | 543 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | MSRES others(538): Show |
chr22 | 28682743 | 28746820 |
| a0008 | 0/0 | 543 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | MSRES others(538): Show |
chr22 | 28682743 | 28746820 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1629 | 360 | 80 | 67 | 155 | 15 | 41 | CHEK2_chr22_28682743_28746820 | CHEK2 | ATGTC others(1624): Show |
chr22 | 28682743 | 28746820 | ||
| a0001c0002 | 0/0 | 1629 | 14 | 5 | 0 | 8 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | ATGTC others(1624): Show |
chr22 | 28682743 | 28746820 | ||
| a0001c0003 | 0/0 | 1629 | 2 | 0 | 0 | 2 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ATGTC others(1624): Show |
chr22 | 28682743 | 28746820 | ||
| a0001c0004 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ATGTC others(1624): Show |
chr22 | 28682743 | 28746820 | ||
| a0002c0005 | 0/0 | 1629 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ATGTC others(1624): Show |
chr22 | 28682743 | 28746820 | ||
| a0003c0009 | 0/0 | 1629 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ATGTC others(1624): Show |
chr22 | 28682743 | 28746820 | ||
| a0004c0007 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ATGTC others(1624): Show |
chr22 | 28682743 | 28746820 | ||
| a0005c0006 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ATGTC others(1624): Show |
chr22 | 28682743 | 28746820 | ||
| a0006c0011 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ATGTC others(1624): Show |
chr22 | 28682743 | 28746820 | ||
| a0007c0010 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ATGTC others(1624): Show |
chr22 | 28682743 | 28746820 | ||
| a0008c0008 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ATGTC others(1624): Show |
chr22 | 28682743 | 28746820 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1844 | 359 | 80 | 66 | 155 | 15 | 41 | CHEK2_chr22_28682743_28746820 | CHEK2 | ACTCT others(1839): Show |
chr22 | 28682743 | 28746820 |
| a0001c0001t0003 | 0/0 | 1844 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ACTCT others(1839): Show |
chr22 | 28682743 | 28746820 |
| a0001c0002t0001 | 0/0 | 1844 | 12 | 3 | 0 | 8 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | ACTCT others(1839): Show |
chr22 | 28682743 | 28746820 |
| a0001c0002t0002 | 0/0 | 1844 | 2 | 2 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ACTCT others(1839): Show |
chr22 | 28682743 | 28746820 |
| a0001c0003t0001 | 0/0 | 1844 | 2 | 0 | 0 | 2 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ACTCT others(1839): Show |
chr22 | 28682743 | 28746820 |
| a0001c0004t0001 | 0/0 | 1844 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ACTCT others(1839): Show |
chr22 | 28682743 | 28746820 |
| a0002c0005t0001 | 0/0 | 1844 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ACTCT others(1839): Show |
chr22 | 28682743 | 28746820 |
| a0003c0009t0001 | 0/0 | 1844 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ACTCT others(1839): Show |
chr22 | 28682743 | 28746820 |
| a0004c0007t0001 | 0/0 | 1844 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ACTCT others(1839): Show |
chr22 | 28682743 | 28746820 |
| a0005c0006t0001 | 0/0 | 1844 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ACTCT others(1839): Show |
chr22 | 28682743 | 28746820 |
| a0006c0011t0001 | 0/0 | 1844 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ACTCT others(1839): Show |
chr22 | 28682743 | 28746820 |
| a0007c0010t0001 | 0/0 | 1844 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ACTCT others(1839): Show |
chr22 | 28682743 | 28746820 |
| a0008c0008t0001 | 0/0 | 1844 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | ACTCT others(1839): Show |
chr22 | 28682743 | 28746820 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0349 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0002g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0002t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0001c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0002c0005t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0003c0009t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0004c0007t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0005c0006t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0006c0011t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0007c0010t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| a0008c0008t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00323 | hp1 | a0002 | c0005 | t0001 | g0219 | EUR | FIN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0364 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00621 | hp1 | a0001 | c0004 | t0001 | g0269 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0369 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | CHS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0352 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0372 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0373 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0379 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0344 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01978 | hp1 | a0003 | c0009 | t0001 | g0293 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0368 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0377 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0367 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02132 | hp1 | a0004 | c0007 | t0001 | g0297 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | CDX | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CDX | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0343 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0371 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0365 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0341 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0375 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02818 | hp2 | a0005 | c0006 | t0001 | g0136 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03130 | hp2 | a0006 | c0011 | t0001 | g0039 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0376 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0378 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03540 | hp2 | a0007 | c0010 | t0001 | g0374 | AFR | GWD | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0351 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0360 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0356 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | BEB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | STU | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | YRI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18959 | hp2 | a0008 | c0008 | t0001 | g0149 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0074 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0366 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0362 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | LWK | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0363 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | TSI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | GIH | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | GIH | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | ACB | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | USA | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | USA | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | USA | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | LWK | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0349 | REF | REF | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0161 | REF | REF | CHEK2_chr22_28682743_28746820 | CHEK2 | chr22 | 28682743 | 28746820 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:28687932 | T | C | 1 | a0004 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.1597A>G | p.Thr533Ala | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 15/15 | 1655/1844 | 1597/1632 | 533/543 | chr22 | 28687932 | |||
| chr22:28687968 | G | A | 1 | a0008 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.1561C>T | p.Arg521Trp | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 15/15 | 1619/1844 | 1561/1632 | 521/543 | chr22 | 28687968 | |||
| chr22:28689187 | T | C | 1 | a0003 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.1490A>G | p.Asp497Gly | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/15 | 1548/1844 | 1490/1632 | 497/543 | chr22 | 28689187 | |||
| chr22:28695159 | A | C | 1 | a0005 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1343T>G | p.Ile448Ser | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/15 | 1401/1844 | 1343/1632 | 448/543 | chr22 | 28695159 | |||
| chr22:28695839 | T | C | 1 | a0007 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1130A>G | p.Glu377Gly | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 11/15 | 1188/1844 | 1130/1632 | 377/543 | chr22 | 28695839 | |||
| chr22:28725099 | A | G | 1 | a0002 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.470T>C | p.Ile157Thr | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/15 | 528/1844 | 470/1632 | 157/543 | chr22 | 28725099 | |||
| chr22:28734468 | G | A | 1 | a0006 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.254C>T | p.Pro85Leu | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/15 | 312/1844 | 254/1632 | 85/543 | chr22 | 28734468 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:28695766 | A | G | 1 | a0001c0003 | 2 | NA18962.hp2 NA18968.hp1 |
synonymous_variant | LOW | c.1203T>C | p.Thr401Thr | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 11/15 | 1261/1844 | 1203/1632 | 401/543 | chr22 | 28695766 | |||
| chr22:28734470 | T | C | 1 | a0001c0002 | 14 | HG00438.hp2 HG00673.hp1 HG01891.hp2 others(11): Show |
synonymous_variant | LOW | c.252A>G | p.Glu84Glu | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/15 | 310/1844 | 252/1632 | 84/543 | chr22 | 28734470 | |||
| chr22:28734707 | C | T | 1 | a0001c0004 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.15G>A | p.Ser5Ser | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/15 | 73/1844 | 15/1632 | 5/543 | chr22 | 28734707 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:28687868 | A | G | 1 | a0001c0001t0003 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*29T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 15/15 | 29 | chr22 | 28687868 | ||||||
| chr22:28741802 | C | A | 1 | a0001c0002t0002 | 2 | HG01891.hp2 HG03516.hp1 |
5_prime_UTR_variant | MODIFIER | c.-40G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/15 | 7081 | chr22 | 28741802 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:28688154 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1543-168G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688154 | |||||||
| chr22:28688178 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0034 a0001c0001t0001g0345 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1543-192A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688178 | |||||||
| chr22:28688354 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0048 |
3 | HG02258.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1543-368A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688354 | |||||||
| chr22:28688397 | G | A | 24 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0059 others(21): Show |
24 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1543-411C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688397 | |||||||
| chr22:28688606 | T | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0142 a0001c0001t0001g0328 others(2): Show |
5 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542+529A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688606 | |||||||
| chr22:28688817 | T | C | 1 | a0001c0001t0001g0377 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1542+318A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688817 | |||||||
| chr22:28688859 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 |
3 | HG01099.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1542+276A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688859 | |||||||
| chr22:28688972 | C | G | 1 | a0001c0001t0001g0357 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1542+163G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28688972 | |||||||
| chr22:28689124 | A | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0028 others(1): Show |
6 | HG02145.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1542+11T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 14/14 | chr22 | 28689124 | |||||||
| chr22:28689352 | A | G | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1462-137T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689352 | |||||||
| chr22:28689413 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1462-198C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689413 | |||||||
| chr22:28689426 | T | C | 2 | a0001c0001t0001g0329 a0001c0001t0001g0333 |
2 | HG01243.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1462-211A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689426 | |||||||
| chr22:28689654 | A | G | 6 | a0001c0001t0001g0146 a0001c0001t0001g0259 a0001c0001t0001g0260 others(3): Show |
6 | NA18939.hp1 NA18955.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.1462-439T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689654 | |||||||
| chr22:28689713 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1462-498G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689713 | |||||||
| chr22:28689714 | A | T | 1 | a0001c0001t0001g0329 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1462-499T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689714 | |||||||
| chr22:28689715 | C | CTGGATAC others(3): Show |
1 | a0001c0001t0001g0329 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1462-501_1462-500i others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689715 | |||||||
| chr22:28689716 | A | G | 1 | a0001c0001t0001g0329 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1462-501T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689716 | |||||||
| chr22:28689804 | G | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(29): Show |
34 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1462-589C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689804 | |||||||
| chr22:28689822 | A | G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(29): Show |
34 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1462-607T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28689822 | |||||||
| chr22:28690103 | C | G | 9 | a0001c0001t0001g0272 a0001c0002t0001g0362 a0001c0002t0001g0363 others(6): Show |
9 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.1462-888G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690103 | |||||||
| chr22:28690105 | C | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(192): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1462-890G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690105 | |||||||
| chr22:28690141 | A | G | 2 | a0001c0001t0001g0345 a0001c0001t0001g0361 |
2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1462-926T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690141 | |||||||
| chr22:28690214 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1462-999C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690214 | |||||||
| chr22:28690309 | T | C | 2 | a0001c0002t0002g0378 a0001c0002t0002g0379 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1462-1094A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690309 | |||||||
| chr22:28690320 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0277 |
2 | NA18998.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1462-1105G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690320 | |||||||
| chr22:28690366 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(29): Show |
34 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1462-1151G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690366 | |||||||
| chr22:28690542 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0142 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1462-1327G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690542 | |||||||
| chr22:28690560 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0142 a0001c0001t0001g0328 others(2): Show |
5 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1462-1345C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690560 | |||||||
| chr22:28690628 | C | CA | 11 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0162 others(8): Show |
11 | HG00438.hp1 HG01346.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1462-1414dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690628 | |||||||
| chr22:28690628 | CAA | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(29): Show |
34 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1462-1415_1462-141 others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690628 | |||||||
| chr22:28690857 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1462-1642C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690857 | |||||||
| chr22:28690947 | C | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0142 a0001c0001t0001g0328 others(2): Show |
5 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1462-1732G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690947 | |||||||
| chr22:28690952 | TG | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(29): Show |
34 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1462-1738delC | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28690952 | |||||||
| chr22:28691053 | T | C | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(312): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1462-1838A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691053 | |||||||
| chr22:28691108 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1462-1893A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691108 | |||||||
| chr22:28691145 | C | T | 1 | a0001c0001t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1462-1930G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691145 | |||||||
| chr22:28691154 | G | C | 58 | a0001c0001t0001g0011 a0001c0001t0001g0083 a0001c0001t0001g0086 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1462-1939C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691154 | |||||||
| chr22:28691257 | A | C | 1 | a0001c0001t0001g0302 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1462-2042T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691257 | |||||||
| chr22:28691294 | ACATGGTG others(873): Show |
A | 1 | a0001c0001t0001g0294 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1461+1858_1462-208 others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691294 | |||||||
| chr22:28691434 | C | T | 12 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(9): Show |
12 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.1462-2219G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691434 | |||||||
| chr22:28691458 | A | G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(29): Show |
34 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1462-2243T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691458 | |||||||
| chr22:28691460 | A | G | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.1462-2245T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691460 | |||||||
| chr22:28691545 | A | T | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1462-2330T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691545 | |||||||
| chr22:28691598 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1462-2383T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691598 | |||||||
| chr22:28691830 | G | A | 234 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1461+2202C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691830 | |||||||
| chr22:28691841 | G | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1461+2191C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28691841 | |||||||
| chr22:28692095 | A | G | 2 | a0001c0001t0001g0233 a0001c0001t0001g0236 |
2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1461+1937T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692095 | |||||||
| chr22:28692135 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1461+1897A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692135 | |||||||
| chr22:28692136 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1461+1896C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692136 | |||||||
| chr22:28692350 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1461+1682G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692350 | |||||||
| chr22:28692463 | A | G | 11 | a0001c0001t0001g0143 a0001c0001t0001g0272 a0001c0002t0001g0007 others(8): Show |
11 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.1461+1569T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692463 | |||||||
| chr22:28692471 | T | TTTTG | 232 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.1461+1557_1461+156 others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692471 | |||||||
| chr22:28692471 | T | TTTTGTTT others(5): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0028 others(1): Show |
6 | HG02145.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461+1549_1461+156 others(16): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692471 | |||||||
| chr22:28692602 | C | T | 235 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(232): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1461+1430G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692602 | |||||||
| chr22:28692831 | C | G | 240 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1461+1201G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692831 | |||||||
| chr22:28692851 | T | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0196 |
2 | NA18946.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1461+1181A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692851 | |||||||
| chr22:28692914 | C | G | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1461+1118G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28692914 | |||||||
| chr22:28693107 | C | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1461+925G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28693107 | |||||||
| chr22:28693249 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0028 others(1): Show |
6 | HG02145.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461+783C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28693249 | |||||||
| chr22:28693784 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1461+248C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28693784 | |||||||
| chr22:28693858 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0001g0333 |
2 | HG01243.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1461+174G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 13/14 | chr22 | 28693858 | |||||||
| chr22:28694375 | G | A | 194 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(191): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1376-258C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694375 | |||||||
| chr22:28694493 | G | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(289): Show |
296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.1376-376C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694493 | |||||||
| chr22:28694780 | A | C | 28 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(25): Show |
28 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1375+347T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694780 | |||||||
| chr22:28694849 | T | G | 1 | a0001c0002t0001g0021 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1375+278A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694849 | |||||||
| chr22:28694902 | G | A | 34 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(31): Show |
34 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1375+225C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694902 | |||||||
| chr22:28694955 | T | C | 1 | a0001c0001t0001g0355 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1375+172A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694955 | |||||||
| chr22:28694973 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1375+154T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694973 | |||||||
| chr22:28694987 | C | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0168 a0001c0001t0001g0169 others(7): Show |
11 | HG02015.hp1 HG02056.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.1375+140G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28694987 | |||||||
| chr22:28695049 | G | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.1375+78C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 12/14 | chr22 | 28695049 | |||||||
| chr22:28695333 | A | G | 1 | a0001c0001t0001g0309 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1260-91T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 11/14 | chr22 | 28695333 | |||||||
| chr22:28695384 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1260-142G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 11/14 | chr22 | 28695384 | |||||||
| chr22:28696087 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1096-214G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696087 | |||||||
| chr22:28696141 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0032 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1096-268A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696141 | |||||||
| chr22:28696189 | A | T | 1 | a0001c0001t0001g0222 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1096-316T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696189 | |||||||
| chr22:28696193 | C | T | 41 | a0001c0001t0001g0006 a0001c0001t0001g0122 a0001c0001t0001g0123 others(38): Show |
41 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1096-320G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696193 | |||||||
| chr22:28696247 | A | G | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1096-374T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696247 | |||||||
| chr22:28696267 | C | G | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1096-394G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696267 | |||||||
| chr22:28696400 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1095+501C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696400 | |||||||
| chr22:28696604 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1095+297G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696604 | |||||||
| chr22:28696713 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1095+188G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696713 | |||||||
| chr22:28696732 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(17): Show |
20 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1095+169G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696732 | |||||||
| chr22:28696738 | C | T | 5 | a0001c0001t0001g0153 a0001c0001t0001g0295 a0001c0001t0001g0298 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+163G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 10/14 | chr22 | 28696738 | |||||||
| chr22:28697204 | C | A | 1 | a0001c0001t0001g0250 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1009-217G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697204 | |||||||
| chr22:28697251 | A | G | 373 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(370): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1009-264T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697251 | |||||||
| chr22:28697290 | T | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(17): Show |
20 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1009-303A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697290 | |||||||
| chr22:28697572 | CT | C | 8 | a0001c0001t0001g0146 a0001c0001t0001g0229 a0001c0001t0001g0241 others(5): Show |
8 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1009-586delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697572 | |||||||
| chr22:28697574 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1009-587A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697574 | |||||||
| chr22:28697765 | G | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(115): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.1009-778C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697765 | |||||||
| chr22:28697978 | G | C | 1 | a0001c0001t0001g0174 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1009-991C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28697978 | |||||||
| chr22:28698096 | T | A | 230 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(227): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1009-1109A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698096 | |||||||
| chr22:28698228 | T | TA | 45 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0023 others(42): Show |
46 | HG00544.hp1 HG00597.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.1009-1242dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | |||||||
| chr22:28698228 | T | TAAAAAAA others(1): Show |
88 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0122 others(85): Show |
88 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1009-1249_1009-124 others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | |||||||
| chr22:28698228 | T | TAAAAAAA others(2): Show |
17 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0126 others(14): Show |
17 | HG01175.hp2 HG01243.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.1009-1250_1009-124 others(13): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | |||||||
| chr22:28698228 | T | TAAAAAAA others(3): Show |
2 | a0001c0001t0001g0154 a0001c0001t0001g0333 |
2 | HG01891.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1009-1251_1009-124 others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | |||||||
| chr22:28698228 | T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0175 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1009-1254_1009-124 others(17): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | |||||||
| chr22:28698228 | T | TAAAAAAA others(7): Show |
64 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0018 others(61): Show |
64 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.1009-1255_1009-124 others(18): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | |||||||
| chr22:28698228 | T | TAAAAAAA others(8): Show |
39 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(36): Show |
40 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1009-1256_1009-124 others(19): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | |||||||
| chr22:28698228 | T | TAAAAAAA others(9): Show |
4 | a0001c0001t0001g0188 a0001c0001t0001g0192 a0001c0001t0001g0197 others(1): Show |
4 | HG01981.hp2 HG02056.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009-1257_1009-124 others(20): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | |||||||
| chr22:28698228 | T | TAAAAAAA others(10): Show |
1 | a0001c0001t0001g0176 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1009-1258_1009-124 others(21): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | |||||||
| chr22:28698228 | T | TAAAAAAA others(12): Show |
2 | a0001c0001t0001g0184 a0001c0001t0001g0347 |
2 | HG00735.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1009-1260_1009-124 others(23): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | |||||||
| chr22:28698228 | T | TAAAAAAA others(20): Show |
1 | a0001c0002t0001g0366 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1009-1242_1009-124 others(31): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | |||||||
| chr22:28698228 | T | TAAAAAAA others(21): Show |
7 | a0001c0002t0001g0007 a0001c0002t0001g0362 a0001c0002t0001g0363 others(4): Show |
7 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1009-1242_1009-124 others(32): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | |||||||
| chr22:28698228 | T | TAAAAAAA others(26): Show |
1 | a0001c0002t0001g0365 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1009-1242_1009-124 others(37): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698228 | |||||||
| chr22:28698322 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 |
3 | HG01099.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1009-1335C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698322 | |||||||
| chr22:28698356 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1009-1369A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698356 | |||||||
| chr22:28698364 | C | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(108): Show |
112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1009-1377G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698364 | |||||||
| chr22:28698374 | G | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0245 a0001c0001t0001g0267 others(1): Show |
4 | HG02886.hp2 HG02896.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009-1387C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698374 | |||||||
| chr22:28698388 | T | G | 110 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0099 others(107): Show |
110 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1009-1401A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698388 | |||||||
| chr22:28698499 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1008+1339A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698499 | |||||||
| chr22:28698768 | C | G | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1008+1070G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698768 | |||||||
| chr22:28698770 | G | A | 8 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(5): Show |
8 | HG02027.hp1 HG02165.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008+1068C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698770 | |||||||
| chr22:28698786 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1008+1052G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698786 | |||||||
| chr22:28698791 | A | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0135 |
2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1008+1047T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698791 | |||||||
| chr22:28698840 | A | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0062 others(83): Show |
87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.1008+998T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28698840 | |||||||
| chr22:28699362 | C | CT | 76 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0017 others(73): Show |
77 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1008+475dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699362 | |||||||
| chr22:28699362 | CT | C | 203 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(200): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1008+475delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699362 | |||||||
| chr22:28699362 | CTT | C | 18 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0151 others(15): Show |
18 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1008+474_1008+475d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699362 | |||||||
| chr22:28699365 | T | TTC | 15 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0023 others(12): Show |
16 | HG01192.hp1 HG01243.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1008+472_1008+473i others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699365 | |||||||
| chr22:28699370 | T | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0023 others(12): Show |
16 | HG01192.hp1 HG01243.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1008+468A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699370 | |||||||
| chr22:28699397 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1008+441G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699397 | |||||||
| chr22:28699489 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0333 |
2 | HG02602.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1008+349G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699489 | |||||||
| chr22:28699492 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0333 |
2 | HG02602.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1008+346C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699492 | |||||||
| chr22:28699502 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0333 |
2 | HG02602.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1008+336G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699502 | |||||||
| chr22:28699646 | AC | A | 110 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0099 others(107): Show |
110 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1008+191delG | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699646 | |||||||
| chr22:28699654 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1008+184C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699654 | |||||||
| chr22:28699669 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1008+169C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699669 | |||||||
| chr22:28699694 | A | T | 1 | a0001c0001t0001g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1008+144T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699694 | |||||||
| chr22:28699830 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA19088.hp1 | splice_region_variant&intron_variant | LOW | c.1008+8A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 9/14 | chr22 | 28699830 | |||||||
| chr22:28699998 | A | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0092 |
2 | NA18948.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.909-61T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28699998 | |||||||
| chr22:28700211 | C | CT | 21 | a0001c0001t0001g0064 a0001c0001t0001g0098 a0001c0001t0001g0117 others(18): Show |
21 | HG00438.hp1 HG01074.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.909-275dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700211 | |||||||
| chr22:28700373 | G | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(81): Show |
85 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.909-436C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700373 | |||||||
| chr22:28700547 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.909-610A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700547 | |||||||
| chr22:28700701 | C | T | 2 | a0001c0002t0001g0020 a0001c0002t0001g0021 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.909-764G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700701 | |||||||
| chr22:28700705 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.909-768G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700705 | |||||||
| chr22:28700786 | C | CTTTA | 5 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
5 | HG00408.hp1 HG02083.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.909-853_909-850dup others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700786 | |||||||
| chr22:28700853 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.909-916T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28700853 | |||||||
| chr22:28701029 | T | A | 12 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(9): Show |
12 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.909-1092A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701029 | |||||||
| chr22:28701192 | T | TGTGATCA others(3): Show |
2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.909-1265_909-1256d others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701192 | |||||||
| chr22:28701289 | C | A | 1 | a0001c0001t0001g0346 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.909-1352G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701289 | |||||||
| chr22:28701314 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.909-1377C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701314 | |||||||
| chr22:28701618 | T | C | 1 | a0001c0001t0001g0359 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.909-1681A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701618 | |||||||
| chr22:28701785 | G | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0164 |
2 | NA18747.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.908+1720C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701785 | |||||||
| chr22:28701954 | A | AT | 200 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(197): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.908+1550dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701954 | |||||||
| chr22:28701954 | A | ATT | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
68 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.908+1549_908+1550d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28701954 | |||||||
| chr22:28702135 | C | CTG | 10 | a0001c0001t0001g0038 a0001c0001t0001g0101 a0001c0001t0001g0163 others(7): Show |
10 | HG00323.hp1 HG02630.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.908+1368_908+1369d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | |||||||
| chr22:28702135 | C | CTGTG | 31 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0083 others(28): Show |
31 | HG00558.hp2 HG00735.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.908+1366_908+1369d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | |||||||
| chr22:28702135 | C | CTGTGTG | 30 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0050 others(27): Show |
31 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.908+1364_908+1369d others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | |||||||
| chr22:28702135 | C | CTGTGTGT others(1): Show |
35 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0027 others(32): Show |
35 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.908+1362_908+1369d others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | |||||||
| chr22:28702135 | C | CTGTGTGT others(3): Show |
74 | a0001c0001t0001g0012 a0001c0001t0001g0103 a0001c0001t0001g0104 others(71): Show |
74 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.908+1360_908+1369d others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | |||||||
| chr22:28702135 | C | CTGTGTGT others(5): Show |
33 | a0001c0001t0001g0105 a0001c0001t0001g0123 a0001c0001t0001g0124 others(30): Show |
33 | HG01106.hp1 HG01175.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.908+1358_908+1369d others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | |||||||
| chr22:28702135 | C | CTGTGTGT others(7): Show |
14 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0167 others(11): Show |
15 | HG01074.hp2 HG01243.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.908+1356_908+1369d others(16): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | |||||||
| chr22:28702135 | C | CTGTGTGT others(9): Show |
6 | a0001c0001t0001g0006 a0001c0001t0001g0122 a0001c0001t0001g0172 others(3): Show |
6 | HG02735.hp1 HG03654.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+1354_908+1369d others(18): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | |||||||
| chr22:28702135 | C | CTGTGTGT others(11): Show |
3 | a0001c0001t0001g0168 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG02155.hp2 HG02523.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.908+1352_908+1369d others(20): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | |||||||
| chr22:28702135 | C | CTGTGTGT others(13): Show |
1 | a0001c0001t0001g0188 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.908+1350_908+1369d others(22): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | |||||||
| chr22:28702135 | CTG | C | 35 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0022 others(32): Show |
35 | HG00099.hp1 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.908+1368_908+1369d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | |||||||
| chr22:28702135 | CTGTG | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(66): Show |
70 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.908+1366_908+1369d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | |||||||
| chr22:28702135 | CTGTGTG | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0044 others(1): Show |
4 | HG01346.hp2 HG01358.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+1364_908+1369d others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702135 | |||||||
| chr22:28702172 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0320 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.908+1332_908+1333i others(13): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702172 | |||||||
| chr22:28702233 | A | AT | 230 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.908+1271dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702233 | |||||||
| chr22:28702233 | AT | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0033 others(3): Show |
6 | HG02258.hp2 HG02451.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+1271delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702233 | |||||||
| chr22:28702261 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.908+1244G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702261 | |||||||
| chr22:28702290 | A | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0083 a0001c0001t0001g0164 others(3): Show |
6 | HG00438.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+1215T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702290 | |||||||
| chr22:28702299 | C | T | 1 | a0001c0001t0001g0359 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.908+1206G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702299 | |||||||
| chr22:28702301 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0359 |
2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.908+1204G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702301 | |||||||
| chr22:28702324 | C | T | 1 | a0001c0001t0001g0320 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.908+1181G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702324 | |||||||
| chr22:28702331 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0071 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.908+1174A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702331 | |||||||
| chr22:28702383 | A | C | 7 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0365 others(4): Show |
7 | HG00673.hp1 HG02015.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+1122T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702383 | |||||||
| chr22:28702383 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.908+1122T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702383 | |||||||
| chr22:28702384 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.908+1121C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702384 | |||||||
| chr22:28702387 | C | T | 1 | a0002c0005t0001g0219 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.908+1118G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702387 | |||||||
| chr22:28702388 | A | G | 1 | a0002c0005t0001g0219 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.908+1117T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702388 | |||||||
| chr22:28702396 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0160 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.908+1109T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702396 | |||||||
| chr22:28702400 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0160 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.908+1105T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702400 | |||||||
| chr22:28702429 | A | G | 31 | a0001c0001t0001g0016 a0001c0001t0001g0099 a0001c0001t0001g0145 others(28): Show |
31 | HG00673.hp1 HG01123.hp2 HG01975.hp1 others(28): Show |
intron_variant | MODIFIER | c.908+1076T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702429 | |||||||
| chr22:28702436 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0160 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.908+1069G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702436 | |||||||
| chr22:28702444 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.908+1061A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702444 | |||||||
| chr22:28702450 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.908+1055C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702450 | |||||||
| chr22:28702454 | G | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0160 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.908+1051C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702454 | |||||||
| chr22:28702455 | G | A | 2 | a0001c0001t0001g0012 a0001c0002t0001g0343 |
2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.908+1050C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702455 | |||||||
| chr22:28702456 | C | T | 12 | a0001c0001t0001g0016 a0001c0001t0001g0142 a0001c0001t0001g0160 others(9): Show |
12 | HG01891.hp2 HG02109.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.908+1049G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702456 | |||||||
| chr22:28702473 | T | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0137 a0001c0001t0001g0194 |
3 | HG01346.hp2 HG01358.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.908+1032A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702473 | |||||||
| chr22:28702537 | CT | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0019 others(104): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.908+967delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702537 | |||||||
| chr22:28702588 | C | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(66): Show |
70 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.908+917G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702588 | |||||||
| chr22:28702827 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0047 others(1): Show |
4 | HG02055.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+678C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702827 | |||||||
| chr22:28702857 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.908+648A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702857 | |||||||
| chr22:28702942 | T | C | 4 | a0001c0001t0001g0166 a0001c0001t0001g0172 a0001c0001t0001g0197 others(1): Show |
4 | HG03654.hp2 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+563A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28702942 | |||||||
| chr22:28703363 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.908+142A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28703363 | |||||||
| chr22:28703371 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0263 |
2 | NA18955.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.908+134G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28703371 | |||||||
| chr22:28703400 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.908+105C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28703400 | |||||||
| chr22:28703411 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.908+94G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 8/14 | chr22 | 28703411 | |||||||
| chr22:28703766 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(105): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.847-200A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28703766 | |||||||
| chr22:28703962 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.847-396G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28703962 | |||||||
| chr22:28704121 | G | C | 2 | a0001c0001t0001g0282 a0001c0001t0001g0354 |
2 | HG00673.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.847-555C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | |||||||
| chr22:28704121 | G | GAC | 12 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0077 others(9): Show |
12 | HG00099.hp1 HG01975.hp2 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.847-557_847-556dup others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | |||||||
| chr22:28704121 | G | GACAC | 4 | a0001c0001t0001g0026 a0001c0001t0001g0375 a0001c0001t0001g0376 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-559_847-556dup others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | |||||||
| chr22:28704121 | GAC | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(128): Show |
131 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.847-557_847-556del others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | |||||||
| chr22:28704121 | GACAC | G | 28 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0031 others(25): Show |
28 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.847-559_847-556del others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | |||||||
| chr22:28704121 | GACACAC | G | 69 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0103 others(66): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.847-561_847-556del others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | |||||||
| chr22:28704121 | GACACACA others(1): Show |
G | 52 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(49): Show |
53 | HG00323.hp1 HG00558.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.847-563_847-556del others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | |||||||
| chr22:28704121 | GACACACA others(3): Show |
G | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.847-565_847-556del others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | |||||||
| chr22:28704121 | GACACACA others(7): Show |
G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0193 |
3 | HG02015.hp1 HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.847-569_847-556del others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704121 | |||||||
| chr22:28704125 | C | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.847-559G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704125 | |||||||
| chr22:28704127 | C | G | 1 | a0001c0001t0001g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.847-561G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704127 | |||||||
| chr22:28704192 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.847-626G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704192 | |||||||
| chr22:28704205 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.847-639T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704205 | |||||||
| chr22:28704302 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.847-736A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704302 | |||||||
| chr22:28704313 | T | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0078 |
2 | HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.847-747A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704313 | |||||||
| chr22:28704316 | T | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.847-750A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704316 | |||||||
| chr22:28704372 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.847-806C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704372 | |||||||
| chr22:28704458 | G | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
6 | HG01192.hp1 HG02109.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.847-892C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704458 | |||||||
| chr22:28704576 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.847-1010T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704576 | |||||||
| chr22:28704608 | C | T | 1 | a0004c0007t0001g0297 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.847-1042G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704608 | |||||||
| chr22:28704639 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.847-1073G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704639 | |||||||
| chr22:28704678 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.847-1112C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704678 | |||||||
| chr22:28704723 | T | C | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.847-1157A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704723 | |||||||
| chr22:28704727 | C | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0096 |
2 | HG02080.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.847-1161G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704727 | |||||||
| chr22:28704895 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.847-1329T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704895 | |||||||
| chr22:28704901 | C | A | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.847-1335G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704901 | |||||||
| chr22:28704989 | C | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.847-1423G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704989 | |||||||
| chr22:28704997 | G | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.847-1431C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28704997 | |||||||
| chr22:28705078 | CT | C | 119 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0049 others(116): Show |
119 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.847-1513delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705078 | |||||||
| chr22:28705127 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.847-1561C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705127 | |||||||
| chr22:28705319 | C | T | 14 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0032 others(11): Show |
14 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.847-1753G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705319 | |||||||
| chr22:28705369 | A | G | 284 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.847-1803T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705369 | |||||||
| chr22:28705549 | A | C | 1 | a0001c0001t0001g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.847-1983T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705549 | |||||||
| chr22:28705612 | A | G | 119 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0084 others(116): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.847-2046T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705612 | |||||||
| chr22:28705648 | G | A | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.847-2082C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705648 | |||||||
| chr22:28705790 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG02145.hp1 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-2224C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705790 | |||||||
| chr22:28705803 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.847-2237C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705803 | |||||||
| chr22:28705841 | G | A | 119 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0084 others(116): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.847-2275C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705841 | |||||||
| chr22:28705852 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.847-2286C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705852 | |||||||
| chr22:28705968 | A | AAAACT | 29 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(26): Show |
29 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.847-2407_847-2403d others(7): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705968 | |||||||
| chr22:28705968 | A | AAAACTAA others(3): Show |
161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(158): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.847-2412_847-2403d others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705968 | |||||||
| chr22:28705968 | A | AAAACTAA others(8): Show |
162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
163 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.847-2417_847-2403d others(17): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705968 | |||||||
| chr22:28705968 | A | AAAACTAA others(13): Show |
15 | a0001c0001t0001g0016 a0001c0001t0001g0154 a0001c0001t0001g0198 others(12): Show |
15 | HG00597.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.847-2422_847-2403d others(22): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705968 | |||||||
| chr22:28705991 | A | ACTAAACT others(8): Show |
1 | a0001c0001t0001g0300 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.847-2426_847-2425i others(17): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28705991 | |||||||
| chr22:28706064 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA19083.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.847-2498G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706064 | |||||||
| chr22:28706129 | T | C | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(243): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.847-2563A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706129 | |||||||
| chr22:28706296 | G | GCT | 8 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0059 others(5): Show |
8 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.847-2732_847-2731d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706296 | |||||||
| chr22:28706298 | T | TCA | 47 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(44): Show |
47 | HG00323.hp1 HG00558.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.847-2734_847-2733d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706298 | |||||||
| chr22:28706298 | T | TCACA | 3 | a0001c0001t0001g0014 a0001c0001t0001g0073 a0001c0001t0001g0336 |
3 | HG02155.hp1 NA18980.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.847-2736_847-2733d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706298 | |||||||
| chr22:28706298 | TCA | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.847-2734_847-2733d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706298 | |||||||
| chr22:28706298 | TCACA | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0281 a0001c0001t0001g0317 |
3 | HG02273.hp2 HG03831.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.847-2736_847-2733d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706298 | |||||||
| chr22:28706298 | TCACACA | T | 114 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0084 others(111): Show |
114 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.847-2738_847-2733d others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706298 | |||||||
| chr22:28706300 | A | T | 20 | a0001c0001t0001g0043 a0001c0001t0001g0080 a0001c0001t0001g0081 others(17): Show |
20 | HG00544.hp1 HG02486.hp1 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.847-2734T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706300 | |||||||
| chr22:28706332 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.847-2766T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706332 | |||||||
| chr22:28706347 | A | T | 46 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0122 others(43): Show |
46 | HG00621.hp1 HG00642.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.847-2781T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706347 | |||||||
| chr22:28706505 | GTGATCAT others(14): Show |
G | 1 | a0001c0001t0001g0300 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.847-2960_847-2940d others(23): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706505 | |||||||
| chr22:28706550 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0005c0006t0001g0136 |
3 | HG02647.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.847-2984G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706550 | |||||||
| chr22:28706578 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.847-3012C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706578 | |||||||
| chr22:28706657 | G | A | 26 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(23): Show |
26 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.847-3091C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706657 | |||||||
| chr22:28706713 | G | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0092 |
3 | HG03927.hp2 NA18948.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.847-3147C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706713 | |||||||
| chr22:28706717 | G | T | 1 | a0001c0001t0001g0330 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.847-3151C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706717 | |||||||
| chr22:28706780 | C | T | 2 | a0001c0001t0001g0372 a0001c0001t0001g0373 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.847-3214G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706780 | |||||||
| chr22:28706792 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0239 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.846+3214C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706792 | |||||||
| chr22:28706855 | GC | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0330 a0001c0001t0001g0334 others(6): Show |
10 | HG01243.hp2 HG01496.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.846+3150delG | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706855 | |||||||
| chr22:28706857 | A | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0330 a0001c0001t0001g0334 others(6): Show |
10 | HG01243.hp2 HG01496.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.846+3149T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706857 | |||||||
| chr22:28706978 | G | A | 8 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.846+3028C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706978 | |||||||
| chr22:28706979 | G | A | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.846+3027C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28706979 | |||||||
| chr22:28707060 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.846+2946A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707060 | |||||||
| chr22:28707093 | TAGTC | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 |
3 | HG01099.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.846+2909_846+2912d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707093 | |||||||
| chr22:28707229 | G | A | 119 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0084 others(116): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.846+2777C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707229 | |||||||
| chr22:28707252 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.846+2754G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707252 | |||||||
| chr22:28707253 | G | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0375 a0001c0001t0001g0376 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+2753C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707253 | |||||||
| chr22:28707305 | G | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0375 a0001c0001t0001g0376 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+2701C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707305 | |||||||
| chr22:28707353 | T | C | 14 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0154 others(11): Show |
14 | HG01891.hp1 HG02056.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.846+2653A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707353 | |||||||
| chr22:28707465 | C | A | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.846+2541G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707465 | |||||||
| chr22:28707504 | T | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0220 |
2 | HG00280.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.846+2502A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707504 | |||||||
| chr22:28707618 | A | T | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.846+2388T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707618 | |||||||
| chr22:28707781 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.846+2225A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707781 | |||||||
| chr22:28707830 | C | CT | 209 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.846+2175dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707830 | |||||||
| chr22:28707830 | C | CTT | 41 | a0001c0001t0001g0050 a0001c0001t0001g0067 a0001c0001t0001g0103 others(38): Show |
41 | HG00323.hp1 HG00642.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.846+2174_846+2175d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707830 | |||||||
| chr22:28707830 | CT | C | 8 | a0001c0001t0001g0012 a0001c0001t0001g0042 a0001c0001t0001g0048 others(5): Show |
8 | HG02559.hp2 HG02723.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.846+2175delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707830 | |||||||
| chr22:28707923 | G | A | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.846+2083C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707923 | |||||||
| chr22:28707979 | C | T | 8 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.846+2027G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28707979 | |||||||
| chr22:28708003 | A | AT | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.846+2002dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708003 | |||||||
| chr22:28708041 | G | A | 4 | a0001c0002t0001g0007 a0001c0002t0001g0343 a0001c0002t0002g0378 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+1965C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708041 | |||||||
| chr22:28708118 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.846+1888G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708118 | |||||||
| chr22:28708201 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0135 |
2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.846+1805A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708201 | |||||||
| chr22:28708361 | A | ATGTG | 9 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0001c0001t0001g0113 others(6): Show |
10 | HG00140.hp1 HG01175.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.846+1644_846+1645i others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | |||||||
| chr22:28708361 | A | ATGTGTG | 4 | a0001c0001t0001g0109 a0001c0001t0001g0177 a0001c0001t0001g0184 others(1): Show |
4 | HG00099.hp2 HG04228.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+1644_846+1645i others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | |||||||
| chr22:28708361 | A | ATGTGTGT others(1): Show |
25 | a0001c0001t0001g0011 a0001c0001t0001g0076 a0001c0001t0001g0103 others(22): Show |
25 | HG00323.hp2 HG00733.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.846+1644_846+1645i others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | |||||||
| chr22:28708361 | A | ATGTGTGT others(3): Show |
19 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0116 others(16): Show |
19 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.846+1644_846+1645i others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | |||||||
| chr22:28708361 | A | ATGTGTGT others(5): Show |
7 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0176 others(4): Show |
7 | HG00735.hp2 HG02071.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.846+1644_846+1645i others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | |||||||
| chr22:28708361 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0001g0125 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.846+1644_846+1645i others(16): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | |||||||
| chr22:28708361 | A | ATGTGTGT others(9): Show |
2 | a0001c0001t0001g0172 a0001c0001t0001g0185 |
2 | HG01106.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.846+1644_846+1645i others(18): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708361 | |||||||
| chr22:28708363 | A | ATG | 21 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(18): Show |
22 | HG01123.hp1 HG01175.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.846+1641_846+1642d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | |||||||
| chr22:28708363 | A | ATGTG | 17 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0033 others(14): Show |
17 | HG00423.hp2 HG00642.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.846+1639_846+1642d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | |||||||
| chr22:28708363 | A | ATGTGTG | 16 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(13): Show |
17 | HG00280.hp1 HG01099.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.846+1637_846+1642d others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | |||||||
| chr22:28708363 | A | ATGTGTGT others(1): Show |
26 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0031 others(23): Show |
26 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.846+1635_846+1642d others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | |||||||
| chr22:28708363 | A | ATGTGTGT others(3): Show |
21 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0038 others(18): Show |
21 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.846+1633_846+1642d others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | |||||||
| chr22:28708363 | A | ATGTGTGT others(5): Show |
9 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0054 others(6): Show |
9 | HG01981.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.846+1631_846+1642d others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | |||||||
| chr22:28708363 | A | ATGTGTGT others(7): Show |
9 | a0001c0001t0001g0010 a0001c0001t0001g0068 a0001c0001t0001g0070 others(6): Show |
9 | HG00735.hp1 HG01069.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.846+1629_846+1642d others(16): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | |||||||
| chr22:28708363 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0001g0079 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.846+1627_846+1642d others(18): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | |||||||
| chr22:28708363 | A | ATGTGTGT others(11): Show |
1 | a0001c0001t0001g0063 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.846+1625_846+1642d others(20): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | |||||||
| chr22:28708363 | A | G | 69 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0076 others(66): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.846+1643T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | |||||||
| chr22:28708363 | ATG | A | 31 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(28): Show |
31 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.846+1641_846+1642d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708363 | |||||||
| chr22:28708367 | G | GTGTGTGT others(5): Show |
3 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0001g0224 |
3 | HG00280.hp2 HG01928.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.846+1638_846+1639i others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708367 | |||||||
| chr22:28708369 | G | GTGTGTGT others(3): Show |
37 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(34): Show |
37 | HG00323.hp1 HG00558.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.846+1636_846+1637i others(12): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708369 | |||||||
| chr22:28708373 | G | GTGTGTC | 6 | a0001c0002t0001g0007 a0001c0002t0001g0020 a0001c0002t0001g0021 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.846+1632_846+1633i others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708373 | |||||||
| chr22:28708692 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0160 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.846+1314C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708692 | |||||||
| chr22:28708742 | T | G | 1 | a0001c0001t0001g0348 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.846+1264A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708742 | |||||||
| chr22:28708782 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.846+1224A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708782 | |||||||
| chr22:28708866 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.846+1140A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708866 | |||||||
| chr22:28708952 | C | CA | 15 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(12): Show |
15 | HG00423.hp2 HG00544.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.846+1053dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708952 | |||||||
| chr22:28708952 | CA | C | 19 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0048 others(16): Show |
19 | HG00597.hp2 HG00673.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.846+1053delT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708952 | |||||||
| chr22:28708952 | CAA | C | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.846+1052_846+1053d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708952 | |||||||
| chr22:28708963 | A | C | 2 | a0001c0001t0001g0331 a0001c0001t0001g0333 |
2 | HG02602.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.846+1043T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708963 | |||||||
| chr22:28708967 | A | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(233): Show |
238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.846+1039T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708967 | |||||||
| chr22:28708971 | A | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.846+1035T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708971 | |||||||
| chr22:28708979 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.846+1027G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708979 | |||||||
| chr22:28708990 | C | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0032 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.846+1016G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28708990 | |||||||
| chr22:28709029 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.846+977A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709029 | |||||||
| chr22:28709036 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.846+970C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709036 | |||||||
| chr22:28709044 | T | C | 1 | a0001c0001t0001g0357 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.846+962A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709044 | |||||||
| chr22:28709214 | G | C | 7 | a0001c0001t0001g0050 a0001c0001t0001g0222 a0001c0001t0001g0224 others(4): Show |
7 | HG00323.hp1 HG01071.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.846+792C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709214 | |||||||
| chr22:28709231 | A | G | 2 | a0001c0002t0002g0378 a0001c0002t0002g0379 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.846+775T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709231 | |||||||
| chr22:28709279 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.846+727C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709279 | |||||||
| chr22:28709427 | G | C | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.846+579C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709427 | |||||||
| chr22:28709459 | C | A | 4 | a0001c0001t0001g0270 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02027.hp1 HG02165.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+547G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709459 | |||||||
| chr22:28709539 | A | C | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.846+467T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709539 | |||||||
| chr22:28709570 | A | G | 162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
163 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.846+436T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709570 | |||||||
| chr22:28709622 | C | T | 284 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.846+384G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709622 | |||||||
| chr22:28709726 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.846+280G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709726 | |||||||
| chr22:28709864 | C | A | 1 | a0001c0001t0001g0252 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.846+142G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709864 | |||||||
| chr22:28709868 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.846+138C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 7/14 | chr22 | 28709868 | |||||||
| chr22:28710186 | A | G | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.793-127T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28710186 | |||||||
| chr22:28710361 | A | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0005c0006t0001g0136 |
3 | HG02647.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.793-302T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28710361 | |||||||
| chr22:28710559 | G | C | 8 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.793-500C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28710559 | |||||||
| chr22:28710745 | T | C | 125 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0049 others(122): Show |
126 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.793-686A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28710745 | |||||||
| chr22:28710957 | G | C | 125 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0049 others(122): Show |
126 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.793-898C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28710957 | |||||||
| chr22:28710979 | T | C | 8 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.793-920A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28710979 | |||||||
| chr22:28711207 | G | A | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.792+702C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28711207 | |||||||
| chr22:28711405 | C | CA | 4 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
4 | HG01099.hp2 HG01255.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+503dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28711405 | |||||||
| chr22:28711584 | G | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0041 others(9): Show |
12 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.792+325C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28711584 | |||||||
| chr22:28711726 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.792+183T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28711726 | |||||||
| chr22:28711781 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG01257.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.792+128C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 6/14 | chr22 | 28711781 | |||||||
| chr22:28712085 | C | A | 1 | a0001c0001t0001g0356 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.684-68G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712085 | |||||||
| chr22:28712091 | C | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0298 |
2 | HG01123.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.684-74G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712091 | |||||||
| chr22:28712094 | G | GTATTAGA others(16): Show |
28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.684-100_684-78dupT others(22): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712094 | |||||||
| chr22:28712124 | A | C | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.684-107T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712124 | |||||||
| chr22:28712139 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.684-122G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712139 | |||||||
| chr22:28712241 | A | G | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.684-224T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712241 | |||||||
| chr22:28712388 | A | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
4 | HG01243.hp1 HG02723.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.684-371T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712388 | |||||||
| chr22:28712456 | T | C | 34 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(31): Show |
34 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.684-439A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712456 | |||||||
| chr22:28712568 | A | T | 40 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(37): Show |
40 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.684-551T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712568 | |||||||
| chr22:28712707 | G | A | 6 | a0001c0002t0001g0007 a0001c0002t0001g0020 a0001c0002t0001g0021 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-690C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712707 | |||||||
| chr22:28712814 | T | A | 1 | a0001c0001t0001g0345 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.684-797A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28712814 | |||||||
| chr22:28713020 | T | G | 6 | a0001c0002t0001g0007 a0001c0002t0001g0020 a0001c0002t0001g0021 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-1003A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713020 | |||||||
| chr22:28713048 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0103 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.684-1031G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713048 | |||||||
| chr22:28713131 | A | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
6 | HG01192.hp1 HG02109.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.684-1114T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713131 | |||||||
| chr22:28713176 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0216 |
2 | NA18944.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.684-1159T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713176 | |||||||
| chr22:28713194 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.684-1177T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713194 | |||||||
| chr22:28713209 | C | T | 12 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0041 others(9): Show |
12 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.684-1192G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713209 | |||||||
| chr22:28713362 | C | CT | 27 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(24): Show |
27 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.684-1346dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713362 | |||||||
| chr22:28713365 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.684-1348A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713365 | |||||||
| chr22:28713398 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0138 |
2 | HG00544.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.684-1381G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713398 | |||||||
| chr22:28713421 | G | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0103 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.684-1404C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713421 | |||||||
| chr22:28713445 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.684-1428G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713445 | |||||||
| chr22:28713636 | G | A | 22 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(19): Show |
22 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.684-1619C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713636 | |||||||
| chr22:28713697 | T | G | 3 | a0001c0001t0001g0328 a0001c0001t0001g0332 a0001c0001t0001g0371 |
3 | HG02257.hp2 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.684-1680A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713697 | |||||||
| chr22:28713853 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.684-1836C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713853 | |||||||
| chr22:28713923 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.684-1906A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28713923 | |||||||
| chr22:28714014 | T | C | 125 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0049 others(122): Show |
126 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.684-1997A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28714014 | |||||||
| chr22:28714175 | C | T | 1 | a0006c0011t0001g0039 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.684-2158G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28714175 | |||||||
| chr22:28714499 | T | C | 2 | a0001c0001t0001g0372 a0001c0001t0001g0373 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.684-2482A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28714499 | |||||||
| chr22:28714516 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.684-2499C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28714516 | |||||||
| chr22:28714771 | C | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(80): Show |
84 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.684-2754G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28714771 | |||||||
| chr22:28715138 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0160 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.684-3121A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28715138 | |||||||
| chr22:28715380 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.684-3363A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28715380 | |||||||
| chr22:28715397 | T | TTTTA | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(266): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.684-3384_684-3381d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28715397 | |||||||
| chr22:28715530 | T | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0041 others(9): Show |
12 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.684-3513A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28715530 | |||||||
| chr22:28715626 | G | A | 6 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
6 | HG02145.hp1 HG02630.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-3609C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28715626 | |||||||
| chr22:28715688 | C | T | 6 | a0001c0002t0001g0007 a0001c0002t0001g0020 a0001c0002t0001g0021 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-3671G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28715688 | |||||||
| chr22:28716170 | G | A | 2 | a0001c0002t0001g0020 a0001c0002t0001g0021 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.683+3225C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716170 | |||||||
| chr22:28716199 | C | CT | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0043 others(26): Show |
29 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.683+3195dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716199 | |||||||
| chr22:28716199 | CT | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(106): Show |
112 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.683+3195delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716199 | |||||||
| chr22:28716222 | A | T | 1 | a0004c0007t0001g0297 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.683+3173T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716222 | |||||||
| chr22:28716250 | G | A | 12 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0041 others(9): Show |
12 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.683+3145C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716250 | |||||||
| chr22:28716371 | A | G | 4 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG00423.hp2 HG03927.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.683+3024T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716371 | |||||||
| chr22:28716484 | A | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0160 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.683+2911T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716484 | |||||||
| chr22:28716491 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.683+2904G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716491 | |||||||
| chr22:28716612 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.683+2783G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716612 | |||||||
| chr22:28716660 | C | T | 4 | a0001c0002t0001g0007 a0001c0002t0001g0343 a0001c0002t0002g0378 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.683+2735G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716660 | |||||||
| chr22:28716940 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.683+2455C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28716940 | |||||||
| chr22:28717062 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.683+2333A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717062 | |||||||
| chr22:28717155 | GATC | G | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.683+2237_683+2239d others(5): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717155 | |||||||
| chr22:28717235 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.683+2160C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717235 | |||||||
| chr22:28717336 | C | A | 6 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
6 | HG00597.hp2 HG00621.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.683+2059G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717336 | |||||||
| chr22:28717354 | G | A | 2 | a0001c0002t0001g0020 a0001c0002t0001g0021 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.683+2041C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717354 | |||||||
| chr22:28717531 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.683+1864G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717531 | |||||||
| chr22:28717885 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.683+1510C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717885 | |||||||
| chr22:28717937 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.683+1458G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28717937 | |||||||
| chr22:28718013 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA19083.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.683+1382C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718013 | |||||||
| chr22:28718023 | G | C | 2 | a0001c0002t0002g0378 a0001c0002t0002g0379 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.683+1372C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718023 | |||||||
| chr22:28718037 | C | T | 1 | a0001c0001t0001g0326 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.683+1358G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718037 | |||||||
| chr22:28718118 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.683+1277G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718118 | |||||||
| chr22:28718401 | T | A | 6 | a0001c0002t0001g0007 a0001c0002t0001g0020 a0001c0002t0001g0021 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.683+994A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718401 | |||||||
| chr22:28718582 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0041 others(2): Show |
5 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.683+813T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718582 | |||||||
| chr22:28718812 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.683+583C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718812 | |||||||
| chr22:28718837 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.683+558C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718837 | |||||||
| chr22:28718883 | A | AAC | 60 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0044 others(57): Show |
60 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.683+510_683+511dup others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | |||||||
| chr22:28718883 | A | AACAC | 41 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0105 others(38): Show |
42 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.683+508_683+511dup others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | |||||||
| chr22:28718883 | A | AACACAC | 16 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0108 others(13): Show |
16 | HG00099.hp2 HG01106.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.683+506_683+511dup others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | |||||||
| chr22:28718883 | A | AACACACA others(1): Show |
13 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(10): Show |
13 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.683+504_683+511dup others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | |||||||
| chr22:28718883 | A | AACACACA others(3): Show |
1 | a0001c0001t0001g0087 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.683+502_683+511dup others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | |||||||
| chr22:28718883 | AAC | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
76 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.683+510_683+511del others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | |||||||
| chr22:28718883 | AACAC | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(87): Show |
91 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.683+508_683+511del others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | |||||||
| chr22:28718883 | AACACAC | A | 11 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0041 others(8): Show |
11 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.683+506_683+511del others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | |||||||
| chr22:28718883 | AACACACA others(1): Show |
A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0078 a0001c0002t0001g0362 |
3 | HG04228.hp2 NA18994.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.683+504_683+511del others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | |||||||
| chr22:28718883 | AACACACA others(3): Show |
A | 7 | a0001c0002t0001g0363 a0001c0002t0001g0364 a0001c0002t0001g0365 others(4): Show |
7 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.683+502_683+511del others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28718883 | |||||||
| chr22:28719003 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.683+392C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28719003 | |||||||
| chr22:28719047 | C | T | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.683+348G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28719047 | |||||||
| chr22:28719078 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(89): Show |
95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.683+317G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 5/14 | chr22 | 28719078 | |||||||
| chr22:28719499 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0285 |
3 | HG02698.hp1 NA18982.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.593-14C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28719499 | |||||||
| chr22:28719660 | T | C | 1 | a0001c0002t0001g0364 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.593-175A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28719660 | |||||||
| chr22:28719772 | C | A | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.593-287G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28719772 | |||||||
| chr22:28719844 | A | C | 8 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.593-359T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28719844 | |||||||
| chr22:28719975 | T | C | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.593-490A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28719975 | |||||||
| chr22:28720092 | A | AT | 91 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(88): Show |
92 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.593-608dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720092 | |||||||
| chr22:28720092 | A | ATT | 58 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0066 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.593-609_593-608dup others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720092 | |||||||
| chr22:28720092 | AT | A | 122 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0049 others(119): Show |
123 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.593-608delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720092 | |||||||
| chr22:28720251 | C | T | 6 | a0001c0002t0001g0007 a0001c0002t0001g0020 a0001c0002t0001g0021 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.593-766G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720251 | |||||||
| chr22:28720411 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.593-926T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720411 | |||||||
| chr22:28720635 | G | A | 8 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.593-1150C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720635 | |||||||
| chr22:28720806 | T | C | 1 | a0001c0002t0001g0343 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.593-1321A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28720806 | |||||||
| chr22:28721178 | T | C | 1 | a0001c0001t0001g0353 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.593-1693A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721178 | |||||||
| chr22:28721228 | A | T | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.593-1743T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721228 | |||||||
| chr22:28721281 | G | GT | 105 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0025 others(102): Show |
105 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.593-1797dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721281 | |||||||
| chr22:28721281 | G | GTT | 78 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(75): Show |
79 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.593-1798_593-1797d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721281 | |||||||
| chr22:28721281 | G | GTTT | 28 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0120 others(25): Show |
28 | HG01243.hp2 HG01358.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.593-1799_593-1797d others(5): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721281 | |||||||
| chr22:28721281 | G | T | 1 | a0001c0002t0001g0363 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.593-1796C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721281 | |||||||
| chr22:28721282 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.593-1797A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721282 | |||||||
| chr22:28721320 | C | A | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(25): Show |
28 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.593-1835G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721320 | |||||||
| chr22:28721922 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0047 others(1): Show |
4 | HG02055.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.593-2437C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28721922 | |||||||
| chr22:28722259 | CGCCGGGC others(1051): Show |
C | 1 | a0001c0001t0001g0223 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.592+1660_592+2717d others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722259 | |||||||
| chr22:28722332 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.592+2645T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722332 | |||||||
| chr22:28722339 | G | A | 232 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.592+2638C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722339 | |||||||
| chr22:28722397 | G | A | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+2580C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722397 | |||||||
| chr22:28722401 | G | A | 2 | a0001c0001t0001g0372 a0001c0001t0001g0373 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.592+2576C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722401 | |||||||
| chr22:28722428 | T | G | 1 | a0001c0001t0001g0316 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.592+2549A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722428 | |||||||
| chr22:28722533 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.592+2444G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722533 | |||||||
| chr22:28722539 | C | CA | 13 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
13 | HG00673.hp1 HG01175.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.592+2437dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722539 | |||||||
| chr22:28722539 | C | CAA | 8 | a0001c0001t0001g0145 a0001c0001t0001g0165 a0001c0001t0001g0182 others(5): Show |
8 | HG02559.hp1 HG03516.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.592+2436_592+2437d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722539 | |||||||
| chr22:28722539 | CA | C | 156 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(153): Show |
157 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.592+2437delT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722539 | |||||||
| chr22:28722554 | AAAAAAGA others(4): Show |
A | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.592+2412_592+2422d others(13): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722554 | |||||||
| chr22:28722556 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0276 |
2 | HG01261.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.592+2421T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722556 | |||||||
| chr22:28722559 | AG | A | 14 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(11): Show |
14 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.592+2417delC | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722559 | |||||||
| chr22:28722560 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.592+2417C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722560 | |||||||
| chr22:28722575 | G | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.592+2402C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722575 | |||||||
| chr22:28722728 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.592+2249A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722728 | |||||||
| chr22:28722768 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.592+2209T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722768 | |||||||
| chr22:28722974 | C | T | 9 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(6): Show |
9 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.592+2003G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28722974 | |||||||
| chr22:28723024 | C | G | 1 | a0001c0001t0001g0327 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.592+1953G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723024 | |||||||
| chr22:28723215 | T | C | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+1762A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723215 | |||||||
| chr22:28723232 | G | C | 125 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0049 others(122): Show |
126 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.592+1745C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723232 | |||||||
| chr22:28723337 | G | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG02027.hp1 HG02165.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+1640C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723337 | |||||||
| chr22:28723391 | G | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0288 |
2 | HG01255.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.592+1586C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723391 | |||||||
| chr22:28723408 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0103 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.592+1569G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723408 | |||||||
| chr22:28723411 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.592+1566T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723411 | |||||||
| chr22:28723523 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0160 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.592+1454C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723523 | |||||||
| chr22:28723599 | A | AG | 3 | a0001c0001t0001g0085 a0001c0001t0001g0157 a0001c0001t0001g0209 |
3 | NA18948.hp1 NA18992.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.592+1377dupC | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723599 | |||||||
| chr22:28723601 | G | GA | 155 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(152): Show |
156 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.592+1375dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723601 | |||||||
| chr22:28723601 | G | GAA | 21 | a0001c0001t0001g0101 a0001c0001t0001g0124 a0001c0001t0001g0158 others(18): Show |
21 | HG00621.hp1 HG01243.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.592+1374_592+1375d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723601 | |||||||
| chr22:28723602 | A | G | 15 | a0001c0001t0001g0146 a0001c0001t0001g0208 a0001c0001t0001g0210 others(12): Show |
15 | NA18939.hp1 NA18944.hp1 NA18944.hp2 others(12): Show |
intron_variant | MODIFIER | c.592+1375T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723602 | |||||||
| chr22:28723609 | AAG | A | 7 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(4): Show |
7 | HG00438.hp2 HG02015.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.592+1366_592+1367d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723609 | |||||||
| chr22:28723610 | AG | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0058 others(3): Show |
6 | HG00673.hp1 HG01081.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.592+1366delC | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723610 | |||||||
| chr22:28723611 | G | A | 351 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(348): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.592+1366C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723611 | |||||||
| chr22:28723663 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.592+1314C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723663 | |||||||
| chr22:28723684 | C | A | 1 | a0001c0001t0001g0283 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.592+1293G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723684 | |||||||
| chr22:28723810 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.592+1167C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723810 | |||||||
| chr22:28723813 | G | A | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+1164C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723813 | |||||||
| chr22:28723930 | T | C | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+1047A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723930 | |||||||
| chr22:28723998 | G | C | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+979C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28723998 | |||||||
| chr22:28724145 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0196 |
2 | NA18946.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.592+832G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724145 | |||||||
| chr22:28724146 | G | A | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+831C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724146 | |||||||
| chr22:28724159 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.592+818C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724159 | |||||||
| chr22:28724235 | G | A | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+742C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724235 | |||||||
| chr22:28724412 | A | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(37): Show |
40 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.592+565T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724412 | |||||||
| chr22:28724418 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.592+559T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724418 | |||||||
| chr22:28724501 | G | C | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+476C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724501 | |||||||
| chr22:28724616 | G | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
6 | HG01192.hp1 HG02109.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.592+361C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724616 | |||||||
| chr22:28724698 | C | G | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.592+279G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724698 | |||||||
| chr22:28724809 | A | G | 40 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(37): Show |
40 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.592+168T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724809 | |||||||
| chr22:28724878 | T | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | NA18981.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.592+99A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724878 | |||||||
| chr22:28724888 | A | T | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | NA18981.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.592+89T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 4/14 | chr22 | 28724888 | |||||||
| chr22:28725488 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.320-121C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725488 | |||||||
| chr22:28725680 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0135 |
3 | HG01496.hp2 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.320-313C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725680 | |||||||
| chr22:28725768 | G | T | 6 | a0001c0002t0001g0007 a0001c0002t0001g0020 a0001c0002t0001g0021 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-401C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725768 | |||||||
| chr22:28725772 | G | C | 125 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0049 others(122): Show |
126 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.320-405C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725772 | |||||||
| chr22:28725864 | G | A | 2 | a0001c0001t0001g0346 a0001c0001t0001g0352 |
2 | HG00741.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.320-497C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725864 | |||||||
| chr22:28725908 | C | CA | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.320-542dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725908 | |||||||
| chr22:28725908 | C | CAA | 14 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0084 others(11): Show |
14 | HG00642.hp1 HG01358.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.320-543_320-542dup others(2): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725908 | |||||||
| chr22:28725922 | T | C | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.320-555A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28725922 | |||||||
| chr22:28726159 | C | T | 8 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.320-792G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726159 | |||||||
| chr22:28726173 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.320-806T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726173 | |||||||
| chr22:28726210 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.320-843T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726210 | |||||||
| chr22:28726380 | T | C | 1 | a0001c0001t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320-1013A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726380 | |||||||
| chr22:28726469 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.320-1102T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726469 | |||||||
| chr22:28726495 | T | A | 1 | a0001c0001t0001g0334 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.320-1128A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726495 | |||||||
| chr22:28726763 | C | T | 1 | a0001c0002t0001g0007 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.320-1396G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726763 | |||||||
| chr22:28726847 | C | A | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.320-1480G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28726847 | |||||||
| chr22:28727215 | G | A | 2 | a0001c0001t0001g0375 a0001c0001t0001g0376 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.320-1848C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727215 | |||||||
| chr22:28727250 | A | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.320-1883T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727250 | |||||||
| chr22:28727402 | A | T | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.320-2035T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727402 | |||||||
| chr22:28727593 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0137 |
2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.320-2226A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727593 | |||||||
| chr22:28727664 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.320-2297G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727664 | |||||||
| chr22:28727687 | T | C | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.320-2320A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727687 | |||||||
| chr22:28727807 | T | G | 17 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0208 others(14): Show |
17 | NA18939.hp1 NA18944.hp1 NA18944.hp2 others(14): Show |
intron_variant | MODIFIER | c.320-2440A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727807 | |||||||
| chr22:28727858 | T | A | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(234): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.320-2491A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727858 | |||||||
| chr22:28727883 | C | CG | 18 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0034 others(15): Show |
18 | HG00673.hp1 HG00735.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.320-2517dupC | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28727883 | |||||||
| chr22:28728002 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.320-2635G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728002 | |||||||
| chr22:28728005 | A | G | 366 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(363): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.320-2638T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728005 | |||||||
| chr22:28728005 | A | T | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.320-2638T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728005 | |||||||
| chr22:28728196 | C | G | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.320-2829G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728196 | |||||||
| chr22:28728290 | TAAAAAGA others(11): Show |
T | 1 | a0001c0001t0001g0148 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.320-2941_320-2924d others(20): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728290 | |||||||
| chr22:28728302 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.320-2935A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728302 | |||||||
| chr22:28728422 | G | A | 8 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.320-3055C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728422 | |||||||
| chr22:28728787 | T | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG00558.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.320-3420A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728787 | |||||||
| chr22:28728829 | A | C | 1 | a0001c0001t0001g0217 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.320-3462T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728829 | |||||||
| chr22:28728898 | A | G | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.320-3531T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728898 | |||||||
| chr22:28728956 | A | AAC | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.320-3590_320-3589i others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728956 | |||||||
| chr22:28728972 | C | CT | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(12): Show |
15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.320-3606dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728972 | |||||||
| chr22:28728974 | C | A | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(12): Show |
15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.320-3607G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728974 | |||||||
| chr22:28728974 | C | CA | 356 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(353): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.320-3608dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28728974 | |||||||
| chr22:28729088 | G | A | 50 | a0001c0001t0001g0049 a0001c0001t0001g0126 a0001c0001t0001g0151 others(47): Show |
50 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.320-3721C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729088 | |||||||
| chr22:28729425 | C | T | 4 | a0001c0002t0001g0007 a0001c0002t0001g0343 a0001c0002t0002g0378 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-4058G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729425 | |||||||
| chr22:28729434 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.320-4067G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729434 | |||||||
| chr22:28729494 | G | GATCACGC others(4): Show |
1 | a0001c0001t0001g0148 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.320-4138_320-4128d others(13): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729494 | |||||||
| chr22:28729522 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0345 a0001c0001t0001g0361 |
3 | HG02559.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.320-4155C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729522 | |||||||
| chr22:28729540 | C | CA | 12 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0024 others(9): Show |
12 | HG01099.hp2 HG01255.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.320-4174dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | |||||||
| chr22:28729540 | C | CAAAAAAA others(5): Show |
2 | a0001c0002t0002g0378 a0001c0002t0002g0379 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.320-4185_320-4174d others(14): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | |||||||
| chr22:28729540 | C | CAAAAAAA others(6): Show |
2 | a0001c0002t0001g0007 a0001c0002t0001g0343 |
2 | HG02257.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.320-4186_320-4174d others(15): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | |||||||
| chr22:28729540 | C | CAAAAAAA others(7): Show |
1 | a0001c0002t0001g0020 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.320-4187_320-4174d others(16): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | |||||||
| chr22:28729540 | C | CAAAAAAA others(8): Show |
1 | a0001c0002t0001g0021 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.320-4188_320-4174d others(17): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | |||||||
| chr22:28729540 | C | CAAAAAAA others(10): Show |
3 | a0001c0002t0001g0363 a0001c0002t0001g0364 a0001c0002t0001g0365 |
3 | HG00438.hp2 HG02523.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.320-4190_320-4174d others(19): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | |||||||
| chr22:28729540 | C | CAAAAAAA others(11): Show |
3 | a0001c0002t0001g0366 a0001c0002t0001g0367 a0001c0002t0001g0368 |
3 | HG02015.hp2 HG02129.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.320-4191_320-4174d others(20): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | |||||||
| chr22:28729540 | C | CAAAAAAA others(16): Show |
1 | a0001c0002t0001g0362 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.320-4196_320-4174d others(25): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | |||||||
| chr22:28729540 | C | CAAAAAAA others(25): Show |
1 | a0001c0002t0001g0369 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.320-4174_320-4173i others(34): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | |||||||
| chr22:28729540 | CAAAA | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0103 a0001c0001t0001g0115 others(20): Show |
24 | HG00738.hp1 HG01433.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.320-4177_320-4174d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | |||||||
| chr22:28729540 | CAAAAA | C | 206 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.320-4178_320-4174d others(7): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | |||||||
| chr22:28729540 | CAAAAAA | C | 7 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0171 others(4): Show |
7 | HG01943.hp1 HG02698.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-4179_320-4174d others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | |||||||
| chr22:28729540 | CAAAAAAA others(1): Show |
C | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(12): Show |
15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.320-4181_320-4174d others(10): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729540 | |||||||
| chr22:28729566 | G | T | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(12): Show |
15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.320-4199C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729566 | |||||||
| chr22:28729579 | A | C | 18 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0208 others(15): Show |
18 | HG02683.hp2 NA18939.hp1 NA18944.hp1 others(15): Show |
intron_variant | MODIFIER | c.320-4212T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729579 | |||||||
| chr22:28729742 | T | G | 372 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(369): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.320-4375A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729742 | |||||||
| chr22:28729927 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.319+4476A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729927 | |||||||
| chr22:28729984 | C | T | 1 | a0001c0001t0001g0360 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.319+4419G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28729984 | |||||||
| chr22:28730001 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.319+4402C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730001 | |||||||
| chr22:28730209 | A | C | 1 | a0001c0001t0001g0014 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.319+4194T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730209 | |||||||
| chr22:28730236 | GAA | G | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+4165_319+4166d others(4): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730236 | |||||||
| chr22:28730240 | A | AGAGGAGG others(6): Show |
1 | a0001c0001t0001g0143 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.319+4162_319+4163i others(15): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730240 | |||||||
| chr22:28730241 | G | T | 3 | a0001c0002t0001g0007 a0001c0002t0002g0378 a0001c0002t0002g0379 |
3 | HG01891.hp2 HG03516.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.319+4162C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730241 | |||||||
| chr22:28730252 | A | G | 8 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.319+4151T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730252 | |||||||
| chr22:28730263 | G | GAGGAGAG others(180): Show |
1 | a0001c0001t0001g0014 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.319+4139_319+4140i others(189): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730263 | |||||||
| chr22:28730264 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.319+4139C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(173): Show |
4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG00741.hp2 HG01168.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(182): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(188): Show |
4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0047 others(1): Show |
4 | HG02055.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(197): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(178): Show |
1 | a0001c0003t0001g0052 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(187): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(178): Show |
66 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(63): Show |
67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(187): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(183): Show |
23 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(20): Show |
25 | HG01192.hp1 HG02055.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(192): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(179): Show |
4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG00735.hp1 HG00738.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(188): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(184): Show |
1 | a0001c0001t0001g0036 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(193): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(179): Show |
1 | a0001c0001t0001g0066 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(188): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(173): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0160 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.319+4138_319+4139i others(182): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(159): Show |
1 | a0001c0001t0001g0170 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(168): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(179): Show |
1 | a0001c0001t0001g0098 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(188): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(179): Show |
1 | a0001c0001t0001g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(188): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(178): Show |
1 | a0001c0001t0001g0061 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(187): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(183): Show |
1 | a0001c0001t0001g0245 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(192): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(155): Show |
13 | a0001c0001t0001g0043 a0001c0001t0001g0101 a0001c0001t0001g0230 others(10): Show |
13 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(164): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(173): Show |
2 | a0001c0001t0001g0044 a0001c0001t0001g0137 |
2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.319+4138_319+4139i others(182): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(149): Show |
1 | a0001c0001t0001g0282 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(158): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(132): Show |
1 | a0001c0001t0001g0228 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(141): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(160): Show |
5 | a0001c0002t0001g0007 a0001c0002t0001g0021 a0001c0002t0001g0343 others(2): Show |
5 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(169): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(165): Show |
1 | a0001c0001t0001g0147 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(174): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(131): Show |
15 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0105 others(12): Show |
15 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(140): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(136): Show |
42 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0145 others(39): Show |
43 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(145): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(151): Show |
1 | a0001c0001t0001g0167 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(160): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(137): Show |
1 | a0001c0001t0001g0346 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(146): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(137): Show |
38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(35): Show |
38 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(146): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(142): Show |
2 | a0001c0001t0001g0342 a0001c0001t0001g0358 |
2 | HG03710.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.319+4138_319+4139i others(151): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(144): Show |
1 | a0001c0001t0001g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(153): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(147): Show |
109 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0122 others(106): Show |
110 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(156): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(152): Show |
2 | a0001c0001t0001g0247 a0001c0001t0001g0280 |
2 | NA18947.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.319+4138_319+4139i others(161): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(162): Show |
2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.319+4138_319+4139i others(171): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(138): Show |
1 | a0001c0001t0001g0263 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(147): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(148): Show |
6 | a0001c0001t0001g0049 a0001c0001t0001g0156 a0001c0001t0001g0281 others(3): Show |
6 | HG00733.hp2 HG01261.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(157): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(137): Show |
1 | a0001c0001t0001g0168 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(146): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(137): Show |
1 | a0001c0001t0001g0348 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(146): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(152): Show |
1 | a0001c0001t0001g0283 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(161): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(137): Show |
1 | a0001c0001t0001g0196 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(146): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(136): Show |
1 | a0001c0001t0001g0103 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(145): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(148): Show |
1 | a0001c0001t0001g0284 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(157): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGAGAG others(149): Show |
1 | a0001c0001t0001g0203 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(158): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGGGAG others(206): Show |
3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+4138_319+4139i others(215): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGGGAG others(165): Show |
1 | a0001c0002t0001g0020 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(174): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGGGAG others(141): Show |
1 | a0001c0001t0001g0169 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.319+4138_319+4139i others(150): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGGGAG others(132): Show |
8 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.319+4138_319+4139i others(141): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730264 | G | GAGGGGAG others(168): Show |
1 | a0001c0001t0001g0143 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.319+4138_319+4139i others(177): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730264 | |||||||
| chr22:28730269 | A | G | 1 | a0001c0001t0001g0327 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.319+4134T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730269 | |||||||
| chr22:28730271 | G | GGAGAGGA others(125): Show |
1 | a0001c0001t0001g0327 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.319+4131_319+4132i others(134): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730271 | |||||||
| chr22:28730274 | A | G | 1 | a0001c0001t0001g0327 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.319+4129T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730274 | |||||||
| chr22:28730277 | C | T | 1 | a0001c0001t0001g0327 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.319+4126G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730277 | |||||||
| chr22:28730316 | CAGAAG | C | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+4082_319+4086d others(7): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730316 | |||||||
| chr22:28730326 | A | G | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+4077T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730326 | |||||||
| chr22:28730359 | GAAAGGA | G | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(12): Show |
15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.319+4038_319+4043d others(8): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730359 | |||||||
| chr22:28730629 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0160 a0001c0002t0001g0007 |
3 | HG02109.hp1 HG04184.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.319+3774C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730629 | |||||||
| chr22:28730726 | C | CATA | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+3674_319+3676d others(5): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730726 | |||||||
| chr22:28730782 | C | T | 17 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0043 others(14): Show |
17 | HG01346.hp2 HG01358.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.319+3621G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28730782 | |||||||
| chr22:28731073 | C | T | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+3330G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731073 | |||||||
| chr22:28731159 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.319+3244A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731159 | |||||||
| chr22:28731207 | TAAAC | T | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+3192_319+3195d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731207 | |||||||
| chr22:28731236 | A | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0162 others(34): Show |
38 | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.319+3167T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731236 | |||||||
| chr22:28731317 | G | A | 1 | a0001c0002t0002g0378 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.319+3086C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731317 | |||||||
| chr22:28731325 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.319+3078C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731325 | |||||||
| chr22:28731369 | C | T | 1 | a0001c0002t0001g0362 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.319+3034G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731369 | |||||||
| chr22:28731414 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.319+2989A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731414 | |||||||
| chr22:28731424 | A | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(126): Show |
132 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.319+2979T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731424 | |||||||
| chr22:28731427 | C | T | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+2976G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731427 | |||||||
| chr22:28731442 | A | T | 1 | a0001c0001t0001g0198 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.319+2961T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731442 | |||||||
| chr22:28731559 | G | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0103 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.319+2844C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731559 | |||||||
| chr22:28731630 | CTATT | C | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+2769_319+2772d others(6): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731630 | |||||||
| chr22:28731964 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.319+2439G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28731964 | |||||||
| chr22:28732025 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.319+2378A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732025 | |||||||
| chr22:28732099 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.319+2304C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732099 | |||||||
| chr22:28732135 | G | T | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+2268C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732135 | |||||||
| chr22:28732402 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.319+2001G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732402 | |||||||
| chr22:28732509 | C | T | 39 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(36): Show |
39 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.319+1894G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732509 | |||||||
| chr22:28732526 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.319+1877G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732526 | |||||||
| chr22:28732545 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.319+1858A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732545 | |||||||
| chr22:28732630 | A | ATTG | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+1772_319+1773i others(5): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732630 | |||||||
| chr22:28732807 | G | A | 2 | a0001c0002t0001g0020 a0001c0002t0001g0021 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.319+1596C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732807 | |||||||
| chr22:28732814 | G | GA | 8 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0024 others(5): Show |
8 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.319+1588dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732814 | |||||||
| chr22:28732829 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.319+1574A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732829 | |||||||
| chr22:28732839 | C | T | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+1564G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732839 | |||||||
| chr22:28732883 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.319+1520G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732883 | |||||||
| chr22:28732901 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.319+1502G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28732901 | |||||||
| chr22:28733252 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.319+1151C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733252 | |||||||
| chr22:28733372 | T | C | 8 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.319+1031A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733372 | |||||||
| chr22:28733652 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.319+751G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733652 | |||||||
| chr22:28733737 | G | T | 1 | a0001c0001t0001g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.319+666C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733737 | |||||||
| chr22:28733753 | T | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(37): Show |
40 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.319+650A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733753 | |||||||
| chr22:28733900 | C | A | 1 | a0001c0001t0001g0322 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.319+503G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733900 | |||||||
| chr22:28733922 | C | CA | 23 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(20): Show |
23 | HG00423.hp1 HG00621.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.319+480dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733922 | |||||||
| chr22:28733922 | CA | C | 19 | a0001c0001t0001g0049 a0001c0001t0001g0058 a0001c0001t0001g0059 others(16): Show |
19 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.319+480delT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28733922 | |||||||
| chr22:28734011 | T | C | 1 | a0001c0001t0001g0327 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.319+392A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28734011 | |||||||
| chr22:28734024 | T | C | 266 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(263): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.319+379A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28734024 | |||||||
| chr22:28734093 | A | G | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+310T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28734093 | |||||||
| chr22:28734224 | T | C | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.319+179A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28734224 | |||||||
| chr22:28734312 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(99): Show |
103 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.319+91G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28734312 | |||||||
| chr22:28734359 | G | GT | 109 | a0001c0001t0001g0049 a0001c0001t0001g0122 a0001c0001t0001g0123 others(106): Show |
109 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.319+43dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 2/14 | chr22 | 28734359 | |||||||
| chr22:28734825 | G | GA | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(106): Show |
112 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-6-99dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28734825 | |||||||
| chr22:28734825 | GA | G | 6 | a0001c0001t0001g0142 a0001c0001t0001g0158 a0001c0001t0001g0267 others(3): Show |
6 | HG02559.hp2 HG02886.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-99delT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28734825 | |||||||
| chr22:28734835 | A | C | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-6-108T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28734835 | |||||||
| chr22:28734917 | G | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
6 | HG01192.hp1 HG02109.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-190C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28734917 | |||||||
| chr22:28734965 | G | A | 2 | a0001c0002t0002g0378 a0001c0002t0002g0379 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-6-238C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28734965 | |||||||
| chr22:28735141 | T | C | 266 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(263): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.-6-414A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735141 | |||||||
| chr22:28735146 | T | G | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-419A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735146 | |||||||
| chr22:28735275 | G | A | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-548C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735275 | |||||||
| chr22:28735359 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-6-632A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735359 | |||||||
| chr22:28735405 | CA | C | 8 | a0001c0001t0001g0057 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-679delT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735405 | |||||||
| chr22:28735409 | A | G | 1 | a0001c0002t0001g0362 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-6-682T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735409 | |||||||
| chr22:28735436 | A | G | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-709T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735436 | |||||||
| chr22:28735438 | T | A | 126 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0049 others(123): Show |
127 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.-6-711A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735438 | |||||||
| chr22:28735800 | C | T | 265 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(262): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.-6-1073G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735800 | |||||||
| chr22:28735902 | A | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0160 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-6-1175T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28735902 | |||||||
| chr22:28736262 | A | G | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-1535T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736262 | |||||||
| chr22:28736350 | C | T | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(12): Show |
15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-6-1623G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736350 | |||||||
| chr22:28736355 | A | AC | 8 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0056 others(5): Show |
8 | HG00597.hp2 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-1629dupG | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736355 | |||||||
| chr22:28736376 | C | A | 8 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-1649G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736376 | |||||||
| chr22:28736385 | T | G | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-1658A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736385 | |||||||
| chr22:28736401 | G | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0103 others(63): Show |
67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.-6-1674C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736401 | |||||||
| chr22:28736405 | A | C | 1 | a0001c0001t0001g0164 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-6-1678T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736405 | |||||||
| chr22:28736414 | T | G | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-1687A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736414 | |||||||
| chr22:28736470 | T | C | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(12): Show |
15 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-6-1743A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736470 | |||||||
| chr22:28736526 | T | C | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-1799A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736526 | |||||||
| chr22:28736547 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-6-1820G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736547 | |||||||
| chr22:28736652 | A | C | 2 | a0001c0002t0002g0378 a0001c0002t0002g0379 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-6-1925T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736652 | |||||||
| chr22:28736717 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-6-1990T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736717 | |||||||
| chr22:28736764 | A | AC | 19 | a0001c0001t0001g0049 a0001c0001t0001g0119 a0001c0001t0001g0138 others(16): Show |
19 | HG00673.hp2 HG00735.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.-6-2038dupG | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736764 | |||||||
| chr22:28736764 | AC | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(103): Show |
107 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-6-2038delG | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736764 | |||||||
| chr22:28736772 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-6-2045G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736772 | |||||||
| chr22:28736773 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-6-2046C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28736773 | |||||||
| chr22:28737002 | A | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(67): Show |
71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.-6-2275T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737002 | |||||||
| chr22:28737041 | G | A | 14 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0137 others(11): Show |
14 | HG01346.hp2 HG01358.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6-2314C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737041 | |||||||
| chr22:28737045 | G | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0103 others(63): Show |
67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.-6-2318C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737045 | |||||||
| chr22:28737096 | A | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | NA18983.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-6-2369T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737096 | |||||||
| chr22:28737324 | C | T | 8 | a0001c0001t0001g0159 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG02056.hp2 HG02080.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6-2597G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737324 | |||||||
| chr22:28737334 | A | T | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-2607T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737334 | |||||||
| chr22:28737474 | CT | C | 9 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
9 | HG01074.hp1 HG01516.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6-2748delA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737474 | |||||||
| chr22:28737492 | G | T | 2 | a0001c0001t0001g0345 a0001c0001t0001g0361 |
2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-6-2765C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737492 | |||||||
| chr22:28737674 | G | A | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6-2947C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28737674 | |||||||
| chr22:28738014 | T | G | 1 | a0001c0001t0001g0340 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-6-3287A>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738014 | |||||||
| chr22:28738315 | C | T | 5 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(2): Show |
5 | HG02572.hp2 HG02896.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+3454G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738315 | |||||||
| chr22:28738350 | G | A | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG01361.hp1 HG01433.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+3419C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738350 | |||||||
| chr22:28738402 | G | C | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG02683.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-7+3367C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738402 | |||||||
| chr22:28738497 | A | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0135 |
2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-7+3272T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738497 | |||||||
| chr22:28738571 | G | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(84): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.-7+3198C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738571 | |||||||
| chr22:28738649 | G | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02622.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-7+3120C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738649 | |||||||
| chr22:28738708 | C | A | 11 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(8): Show |
11 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+3061G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738708 | |||||||
| chr22:28738731 | G | A | 40 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(37): Show |
40 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.-7+3038C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28738731 | |||||||
| chr22:28739133 | G | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(132): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.-7+2636C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28739133 | |||||||
| chr22:28739208 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-7+2561C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28739208 | |||||||
| chr22:28739370 | C | CT | 52 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(49): Show |
52 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-7+2398dupA | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28739370 | |||||||
| chr22:28739532 | T | C | 6 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG02622.hp2 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+2237A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28739532 | |||||||
| chr22:28739555 | G | A | 40 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(37): Show |
40 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.-7+2214C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28739555 | |||||||
| chr22:28739901 | T | C | 142 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0122 others(139): Show |
143 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-7+1868A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28739901 | |||||||
| chr22:28740031 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-7+1738T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740031 | |||||||
| chr22:28740034 | C | G | 1 | a0001c0001t0001g0014 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-7+1735G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740034 | |||||||
| chr22:28740094 | G | A | 3 | a0001c0002t0001g0343 a0001c0002t0002g0378 a0001c0002t0002g0379 |
3 | HG01891.hp2 HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-7+1675C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740094 | |||||||
| chr22:28740144 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-7+1625A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740144 | |||||||
| chr22:28740163 | T | A | 2 | a0001c0001t0001g0345 a0001c0001t0001g0361 |
2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-7+1606A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740163 | |||||||
| chr22:28740199 | C | CA | 5 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0375 others(2): Show |
5 | HG01361.hp1 HG02723.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+1569dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740199 | |||||||
| chr22:28740245 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7+1524G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740245 | |||||||
| chr22:28740267 | A | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0375 a0001c0001t0001g0376 others(1): Show |
4 | HG02723.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+1502T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740267 | |||||||
| chr22:28740532 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-7+1237T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740532 | |||||||
| chr22:28740663 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-7+1106G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740663 | |||||||
| chr22:28740762 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+1007A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740762 | |||||||
| chr22:28740763 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+1006C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740763 | |||||||
| chr22:28740764 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+1005C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740764 | |||||||
| chr22:28740765 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+1004T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740765 | |||||||
| chr22:28740766 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+1003G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740766 | |||||||
| chr22:28740776 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+993A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740776 | |||||||
| chr22:28740780 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+989T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740780 | |||||||
| chr22:28740787 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+982T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740787 | |||||||
| chr22:28740788 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA19083.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-7+981G>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740788 | |||||||
| chr22:28740789 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+980A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740789 | |||||||
| chr22:28740793 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+976G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740793 | |||||||
| chr22:28740797 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+972A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740797 | |||||||
| chr22:28740802 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+967G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740802 | |||||||
| chr22:28740818 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+951T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740818 | |||||||
| chr22:28740819 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+950T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740819 | |||||||
| chr22:28740822 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+947T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740822 | |||||||
| chr22:28740823 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+946C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740823 | |||||||
| chr22:28740824 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+945A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740824 | |||||||
| chr22:28740828 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+941C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740828 | |||||||
| chr22:28740834 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+935T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740834 | |||||||
| chr22:28740851 | G | GATTCCCA others(25): Show |
1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+917_-7+918insAC others(30): Show |
CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740851 | |||||||
| chr22:28740878 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+891C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740878 | |||||||
| chr22:28740884 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+885C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740884 | |||||||
| chr22:28740892 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+877T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740892 | |||||||
| chr22:28740900 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+869T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740900 | |||||||
| chr22:28740909 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+860T>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740909 | |||||||
| chr22:28740910 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+859G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740910 | |||||||
| chr22:28740919 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+850C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740919 | |||||||
| chr22:28740931 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+838C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740931 | |||||||
| chr22:28740954 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+815C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28740954 | |||||||
| chr22:28741107 | G | A | 3 | a0001c0002t0001g0007 a0001c0002t0002g0378 a0001c0002t0002g0379 |
3 | HG01891.hp2 HG03516.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-7+662C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741107 | |||||||
| chr22:28741148 | C | CA | 15 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0348 others(12): Show |
15 | HG00673.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7+620dupT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741148 | |||||||
| chr22:28741148 | CA | C | 15 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(12): Show |
15 | HG00323.hp2 HG01069.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7+620delT | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741148 | |||||||
| chr22:28741169 | A | AG | 9 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
9 | HG01346.hp2 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7+599_-7+600insC | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741169 | |||||||
| chr22:28741169 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(127): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.-7+600T>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741169 | |||||||
| chr22:28741175 | T | C | 8 | a0001c0002t0001g0362 a0001c0002t0001g0363 a0001c0002t0001g0364 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7+594A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741175 | |||||||
| chr22:28741220 | A | T | 1 | a0001c0002t0001g0007 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-7+549T>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741220 | |||||||
| chr22:28741222 | T | A | 1 | a0001c0001t0001g0370 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-7+547A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741222 | |||||||
| chr22:28741228 | T | A | 1 | a0001c0001t0001g0371 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-7+541A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741228 | |||||||
| chr22:28741325 | C | A | 2 | a0001c0001t0001g0372 a0001c0001t0001g0373 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-7+444G>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741325 | |||||||
| chr22:28741331 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0375 a0001c0001t0001g0376 others(1): Show |
4 | HG02723.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+438A>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741331 | |||||||
| chr22:28741364 | G | T | 1 | a0001c0001t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-7+405C>A | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741364 | |||||||
| chr22:28741369 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7+400C>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741369 | |||||||
| chr22:28741456 | G | C | 3 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0007c0010t0001g0374 |
3 | HG02723.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-7+313C>G | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741456 | |||||||
| chr22:28741483 | T | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0375 a0001c0001t0001g0376 others(1): Show |
4 | HG02723.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+286A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741483 | |||||||
| chr22:28741580 | T | A | 1 | a0001c0001t0001g0377 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-7+189A>T | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741580 | |||||||
| chr22:28741742 | C | G | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7+27G>C | CHEK2 | ENSG00000183765.24 | transcript | ENST00000404276.6 | protein_coding | 1/14 | chr22 | 28741742 |