Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5427 |
| ensemblid | ENSG00000100479.14 |
| hgncid | 9178 |
| symbol | POLE2 |
| name | DNA polymerase epsilon 2, accessory subunit |
| refseq_nuc | NM_002692.4 |
| refseq_prot | NP_002683.2 |
| ensembl_nuc | ENST00000216367.10 |
| ensembl_prot | ENSP00000216367.5 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 49643555 |
| end | 49688214 |
| strand | - |
| ver | v1.2 |
| region | chr14:49643555-49688214 |
| region5000 | chr14:49638555-49693214 |
| regionname0 | POLE2_chr14_49643555_49688214 |
| regionname5000 | POLE2_chr14_49638555_49693214 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 527 | 228 | 93 | 50 | 49 | 14 | 20 | 30 | POLE2_chr14_49638555_49693214 | POLE2 | MAPER others(522): Show |
chr14 | 49638555 | 49693214 |
| a0002 | 0/0 | 527 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | MAPER others(522): Show |
chr14 | 49638555 | 49693214 |
| a0003 | 0/0 | 527 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | MAPER others(522): Show |
chr14 | 49638555 | 49693214 |
| a0004 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | MAPER others(522): Show |
chr14 | 49638555 | 49693214 |
| a0005 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | MAPER others(522): Show |
chr14 | 49638555 | 49693214 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1581 | 168 | 48 | 40 | 49 | 12 | 17 | POLE2_chr14_49638555_49693214 | POLE2 | ATGGC others(1576): Show |
chr14 | 49638555 | 49693214 | ||
| a0001c0002 | 0/0 | 1581 | 54 | 39 | 10 | 0 | 2 | 3 | POLE2_chr14_49638555_49693214 | POLE2 | ATGGC others(1576): Show |
chr14 | 49638555 | 49693214 | ||
| a0001c0003 | 0/0 | 1581 | 4 | 4 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | ATGGC others(1576): Show |
chr14 | 49638555 | 49693214 | ||
| a0001c0004 | 0/0 | 1581 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | ATGGC others(1576): Show |
chr14 | 49638555 | 49693214 | ||
| a0002c0005 | 0/0 | 1581 | 2 | 0 | 0 | 2 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | ATGGC others(1576): Show |
chr14 | 49638555 | 49693214 | ||
| a0003c0006 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | ATGGC others(1576): Show |
chr14 | 49638555 | 49693214 | ||
| a0003c0008 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | ATGGC others(1576): Show |
chr14 | 49638555 | 49693214 | ||
| a0004c0009 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | ATGGC others(1576): Show |
chr14 | 49638555 | 49693214 | ||
| a0005c0007 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | ATGGC others(1576): Show |
chr14 | 49638555 | 49693214 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1692 | 160 | 46 | 34 | 49 | 12 | 17 | POLE2_chr14_49638555_49693214 | POLE2 | AAATC others(1687): Show |
chr14 | 49638555 | 49693214 |
| a0001c0001t0002 | 0/0 | 1692 | 8 | 2 | 6 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | AAATC others(1687): Show |
chr14 | 49638555 | 49693214 |
| a0001c0002t0001 | 0/0 | 1692 | 20 | 16 | 4 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | AAATC others(1687): Show |
chr14 | 49638555 | 49693214 |
| a0001c0002t0002 | 0/0 | 1692 | 30 | 22 | 5 | 0 | 1 | 2 | POLE2_chr14_49638555_49693214 | POLE2 | AAATC others(1687): Show |
chr14 | 49638555 | 49693214 |
| a0001c0002t0003 | 0/0 | 1692 | 4 | 1 | 1 | 0 | 1 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | AAATC others(1687): Show |
chr14 | 49638555 | 49693214 |
| a0001c0003t0002 | 0/0 | 1692 | 4 | 4 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | AAATC others(1687): Show |
chr14 | 49638555 | 49693214 |
| a0001c0004t0004 | 0/0 | 1690 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | AAATC others(1685): Show |
chr14 | 49638555 | 49693214 |
| a0002c0005t0002 | 0/0 | 1692 | 2 | 0 | 0 | 2 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | AAATC others(1687): Show |
chr14 | 49638555 | 49693214 |
| a0003c0006t0002 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | AAATC others(1687): Show |
chr14 | 49638555 | 49693214 |
| a0003c0008t0002 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | AAATC others(1687): Show |
chr14 | 49638555 | 49693214 |
| a0004c0009t0002 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | AAATC others(1687): Show |
chr14 | 49638555 | 49693214 |
| a0005c0007t0002 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | AAATC others(1687): Show |
chr14 | 49638555 | 49693214 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0002 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0002t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0003t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0003t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0004t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0001c0004t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0002c0005t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0002c0005t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0003c0006t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0003c0008t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0004c0009t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| a0005c0007t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | GBR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | FIN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | FIN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00597 | hp1 | a0002 | c0005 | t0002 | g0017 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0205 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0183 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0181 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0176 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0153 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0048 | EUR | IBS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01891 | hp1 | a0004 | c0009 | t0002 | g0214 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0185 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0180 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0190 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02145 | hp1 | a0001 | c0002 | t0003 | g0203 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0155 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0173 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02615 | hp1 | a0003 | c0008 | t0002 | g0213 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0057 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0184 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0206 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0171 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0182 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0172 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0187 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0058 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03098 | hp1 | a0001 | c0004 | t0004 | g0026 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03098 | hp2 | a0001 | c0004 | t0004 | g0186 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03139 | hp2 | a0005 | c0007 | t0002 | g0189 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03239 | hp2 | a0001 | c0002 | t0003 | g0169 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03453 | hp1 | a0001 | c0003 | t0002 | g0188 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0178 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0209 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0031 | SAS | PJL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | YRI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0208 | AFR | YRI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | YRI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | YRI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18978 | hp2 | a0003 | c0006 | t0002 | g0015 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19011 | hp1 | a0002 | c0005 | t0002 | g0016 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | LWK | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | LWK | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0170 | EUR | TSI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | GIH | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | GIH | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0177 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | MSL | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | USA | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | USA | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | USA | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | USA | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0018 | REF | REF | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0110 | REF | REF | POLE2_chr14_49638555_49693214 | POLE2 | chr14 | 49638555 | 49693214 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:49650348 | A | G | 1 | a0003 | 2 | HG02615.hp1 NA18978.hp2 |
missense_variant | MODERATE | c.1414T>C | p.Tyr472His | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/19 | 1425/1692 | 1414/1584 | 472/527 | chr14 | 49650348 | |||
| chr14:49654789 | G | C | 1 | a0002 | 2 | HG00597.hp1 NA19011.hp1 |
missense_variant | MODERATE | c.1068C>G | p.His356Gln | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 13/19 | 1079/1692 | 1068/1584 | 356/527 | chr14 | 49654789 | |||
| chr14:49654814 | A | G | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1043T>C | p.Ile348Thr | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 13/19 | 1054/1692 | 1043/1584 | 348/527 | chr14 | 49654814 | |||
| chr14:49688169 | G | A | 1 | a0004 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.35C>T | p.Ser12Phe | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/19 | 46/1692 | 35/1584 | 12/527 | chr14 | 49688169 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:49665128 | G | T | 8 | a0001c0002 a0001c0003 a0001c0004 others(5): Show |
66 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(63): Show |
synonymous_variant | LOW | c.612C>A | p.Val204Val | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 8/19 | 623/1692 | 612/1584 | 204/527 | chr14 | 49665128 | |||
| chr14:49666339 | C | T | 2 | a0003c0006 a0003c0008 |
2 | HG02615.hp1 NA18978.hp2 |
synonymous_variant | LOW | c.567G>A | p.Gln189Gln | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/19 | 578/1692 | 567/1584 | 189/527 | chr14 | 49666339 | |||
| chr14:49666342 | C | T | 2 | a0001c0003 a0005c0007 |
5 | HG02622.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
synonymous_variant | LOW | c.564G>A | p.Thr188Thr | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/19 | 575/1692 | 564/1584 | 188/527 | chr14 | 49666342 | |||
| chr14:49669539 | G | A | 1 | a0001c0004 | 2 | HG03098.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.477C>T | p.Ser159Ser | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/19 | 488/1692 | 477/1584 | 159/527 | chr14 | 49669539 | |||
| chr14:49674162 | T | C | 1 | a0002c0005 | 2 | HG00597.hp1 NA19011.hp1 |
synonymous_variant | LOW | c.378A>G | p.Lys126Lys | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/19 | 389/1692 | 378/1584 | 126/527 | chr14 | 49674162 | |||
| chr14:49688174 | C | G | 1 | a0003c0006 | 1 | NA18978.hp2 | synonymous_variant | LOW | c.30G>C | p.Ala10Ala | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/19 | 41/1692 | 30/1584 | 10/527 | chr14 | 49688174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:49643601 | T | C | 9 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0003 others(6): Show |
52 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*51A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 19/19 | 51 | chr14 | 49643601 | ||||||
| chr14:49643601 | TAG | T | 1 | a0001c0004t0004 | 2 | HG03098.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*49_*50delCT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 19/19 | 49 | chr14 | 49643601 | ||||||
| chr14:49643647 | G | A | 1 | a0001c0002t0003 | 4 | HG00735.hp1 HG02145.hp1 HG03239.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 19/19 | 5 | chr14 | 49643647 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:49643776 | C | T | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1566-106G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49643776 | |||||||
| chr14:49643875 | CT | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(187): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1566-206delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49643875 | |||||||
| chr14:49643875 | CTT | C | 16 | a0001c0002t0002g0003 a0001c0002t0002g0027 a0001c0002t0002g0033 others(13): Show |
18 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1566-207_1566-206d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49643875 | |||||||
| chr14:49643896 | T | C | 9 | a0001c0002t0002g0003 a0001c0002t0002g0027 a0001c0002t0002g0033 others(6): Show |
11 | HG01891.hp2 HG02258.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1566-226A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49643896 | |||||||
| chr14:49643918 | T | C | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1566-248A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49643918 | |||||||
| chr14:49643994 | C | T | 2 | a0003c0006t0002g0015 a0003c0008t0002g0213 |
2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1566-324G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49643994 | |||||||
| chr14:49644178 | G | A | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1566-508C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644178 | |||||||
| chr14:49644308 | C | T | 5 | a0001c0001t0002g0073 a0001c0002t0002g0176 a0001c0002t0002g0180 others(2): Show |
5 | HG00741.hp1 HG01167.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-638G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644308 | |||||||
| chr14:49644309 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1566-639C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644309 | |||||||
| chr14:49644403 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1566-733C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644403 | |||||||
| chr14:49644474 | C | T | 1 | a0001c0004t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1566-804G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644474 | |||||||
| chr14:49644491 | CAA | C | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1566-823_1566-822d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644491 | |||||||
| chr14:49644506 | G | A | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1566-836C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644506 | |||||||
| chr14:49644511 | C | CA | 47 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(44): Show |
51 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1566-842dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644511 | |||||||
| chr14:49644589 | T | C | 2 | a0003c0006t0002g0015 a0003c0008t0002g0213 |
2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1566-919A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644589 | |||||||
| chr14:49644731 | T | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(5): Show |
12 | HG01496.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1566-1061A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644731 | |||||||
| chr14:49644956 | C | T | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1566-1286G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49644956 | |||||||
| chr14:49645043 | C | CA | 8 | a0001c0001t0001g0063 a0001c0001t0001g0090 a0001c0001t0001g0114 others(5): Show |
8 | HG01433.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1566-1374dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | |||||||
| chr14:49645043 | C | CAA | 9 | a0001c0002t0002g0003 a0001c0002t0002g0027 a0001c0002t0002g0033 others(6): Show |
11 | HG00597.hp1 HG01891.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1566-1375_1566-137 others(6): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | |||||||
| chr14:49645043 | C | CAAA | 8 | a0001c0002t0002g0034 a0001c0002t0002g0173 a0001c0003t0002g0057 others(5): Show |
8 | HG02258.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1566-1376_1566-137 others(7): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | |||||||
| chr14:49645043 | C | CAAAAAAA others(3): Show |
1 | a0001c0004t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1566-1383_1566-137 others(14): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | |||||||
| chr14:49645043 | C | CAAAAAAA others(8): Show |
12 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0101 others(9): Show |
13 | HG00735.hp1 HG01167.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1566-1388_1566-137 others(19): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | |||||||
| chr14:49645043 | C | CAAAAAAA others(9): Show |
15 | a0001c0001t0002g0077 a0001c0001t0002g0122 a0001c0002t0002g0014 others(12): Show |
16 | HG00741.hp1 HG01258.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1566-1374_1566-137 others(20): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | |||||||
| chr14:49645043 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0002g0076 a0001c0002t0003g0203 |
2 | HG02145.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1566-1374_1566-137 others(21): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | |||||||
| chr14:49645043 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0002g0078 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1566-1374_1566-137 others(22): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645043 | |||||||
| chr14:49645054 | A | C | 1 | a0001c0001t0001g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1566-1384T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645054 | |||||||
| chr14:49645059 | C | A | 30 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(27): Show |
32 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.1566-1389G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645059 | |||||||
| chr14:49645115 | G | C | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1566-1445C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645115 | |||||||
| chr14:49645262 | TCAC | T | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1566-1595_1566-159 others(7): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645262 | |||||||
| chr14:49645349 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(131): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1566-1679G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645349 | |||||||
| chr14:49645475 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1566-1805G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645475 | |||||||
| chr14:49645499 | G | C | 1 | a0001c0001t0001g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1565+1794C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645499 | |||||||
| chr14:49645657 | C | T | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+1636G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645657 | |||||||
| chr14:49645761 | C | A | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+1532G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645761 | |||||||
| chr14:49645883 | T | G | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1565+1410A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645883 | |||||||
| chr14:49645915 | G | A | 19 | a0001c0001t0001g0036 a0001c0001t0001g0106 a0001c0002t0001g0004 others(16): Show |
20 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1565+1378C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645915 | |||||||
| chr14:49645994 | G | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0049 others(55): Show |
61 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.1565+1299C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49645994 | |||||||
| chr14:49646171 | A | G | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+1122T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646171 | |||||||
| chr14:49646226 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1565+1067C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646226 | |||||||
| chr14:49646290 | G | GC | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+1002_1565+100 others(5): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646290 | |||||||
| chr14:49646302 | G | GT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(38): Show |
47 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1565+990dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | |||||||
| chr14:49646302 | G | GTT | 20 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0054 others(17): Show |
20 | HG00438.hp2 HG01261.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.1565+989_1565+990d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | |||||||
| chr14:49646302 | G | GTTT | 12 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0061 others(9): Show |
12 | HG00099.hp2 HG00639.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1565+988_1565+990d others(5): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | |||||||
| chr14:49646302 | G | GTTTT | 5 | a0001c0001t0001g0050 a0001c0001t0001g0103 a0001c0001t0001g0119 others(2): Show |
5 | HG00280.hp1 HG01192.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1565+987_1565+990d others(6): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | |||||||
| chr14:49646302 | G | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0204 |
3 | HG02630.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1565+991C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | |||||||
| chr14:49646302 | GT | G | 8 | a0001c0002t0001g0037 a0001c0002t0001g0041 a0001c0002t0001g0044 others(5): Show |
8 | HG01099.hp1 HG01358.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1565+990delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | |||||||
| chr14:49646302 | GTTT | G | 13 | a0001c0001t0001g0036 a0001c0001t0001g0106 a0001c0002t0001g0004 others(10): Show |
15 | HG00733.hp2 HG01361.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.1565+988_1565+990d others(5): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | |||||||
| chr14:49646302 | GTTTTTTT others(1): Show |
G | 5 | a0001c0002t0002g0027 a0001c0002t0002g0033 a0001c0002t0002g0034 others(2): Show |
5 | HG00597.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+983_1565+990d others(10): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | |||||||
| chr14:49646302 | GTTTTTTT others(2): Show |
G | 6 | a0001c0002t0002g0003 a0001c0002t0002g0171 a0001c0002t0002g0172 others(3): Show |
8 | HG01891.hp2 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1565+982_1565+990d others(11): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | |||||||
| chr14:49646302 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1565+976_1565+990d others(17): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | |||||||
| chr14:49646302 | GTTTTTTT others(9): Show |
G | 17 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0059 others(14): Show |
20 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1565+975_1565+990d others(18): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | |||||||
| chr14:49646302 | GTTTTTTT others(12): Show |
G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0088 a0001c0001t0001g0192 |
3 | HG00741.hp2 HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1565+972_1565+990d others(21): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646302 | |||||||
| chr14:49646310 | T | TG | 9 | a0001c0001t0002g0078 a0001c0001t0002g0122 a0001c0002t0002g0153 others(6): Show |
9 | HG00741.hp1 HG01258.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.1565+982_1565+983i others(3): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646310 | |||||||
| chr14:49646311 | T | G | 22 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(19): Show |
24 | HG00735.hp1 HG01167.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1565+982A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646311 | |||||||
| chr14:49646312 | T | G | 5 | a0001c0003t0002g0058 a0001c0003t0002g0188 a0003c0006t0002g0015 others(2): Show |
5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+981A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646312 | |||||||
| chr14:49646346 | C | T | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+947G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646346 | |||||||
| chr14:49646472 | G | A | 1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1565+821C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646472 | |||||||
| chr14:49646553 | G | C | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+740C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646553 | |||||||
| chr14:49646573 | G | A | 2 | a0001c0001t0001g0062 a0001c0002t0002g0172 |
2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1565+720C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646573 | |||||||
| chr14:49646643 | G | A | 7 | a0001c0002t0002g0003 a0001c0002t0002g0027 a0001c0002t0002g0171 others(4): Show |
9 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1565+650C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646643 | |||||||
| chr14:49646664 | C | T | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+629G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646664 | |||||||
| chr14:49646678 | A | G | 9 | a0001c0002t0002g0003 a0001c0002t0002g0027 a0001c0002t0002g0033 others(6): Show |
11 | HG01891.hp2 HG02258.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1565+615T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49646678 | |||||||
| chr14:49647114 | A | G | 70 | a0001c0001t0001g0036 a0001c0001t0001g0106 a0001c0001t0002g0006 others(67): Show |
76 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1565+179T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49647114 | |||||||
| chr14:49647170 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1565+123T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49647170 | |||||||
| chr14:49647191 | T | C | 1 | a0001c0002t0002g0033 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1565+102A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49647191 | |||||||
| chr14:49647197 | T | G | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1565+96A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49647197 | |||||||
| chr14:49647230 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1565+63A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 18/18 | chr14 | 49647230 | |||||||
| chr14:49647399 | CT | C | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1498-40delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647399 | |||||||
| chr14:49647407 | T | A | 7 | a0001c0002t0002g0190 a0001c0003t0002g0057 a0001c0003t0002g0058 others(4): Show |
7 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1498-47A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647407 | |||||||
| chr14:49647461 | A | AT | 3 | a0001c0002t0002g0034 a0001c0004t0004g0026 a0002c0005t0002g0017 |
3 | HG00597.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1498-102dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647461 | |||||||
| chr14:49647465 | A | T | 14 | a0001c0002t0002g0003 a0001c0002t0002g0027 a0001c0002t0002g0033 others(11): Show |
16 | HG00597.hp1 HG01891.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1498-105T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647465 | |||||||
| chr14:49647465 | AT | A | 5 | a0001c0002t0002g0190 a0001c0003t0002g0057 a0001c0003t0002g0058 others(2): Show |
5 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498-106delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647465 | |||||||
| chr14:49647541 | T | C | 30 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(27): Show |
32 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.1498-181A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647541 | |||||||
| chr14:49647557 | G | C | 7 | a0001c0002t0002g0003 a0001c0002t0002g0027 a0001c0002t0002g0171 others(4): Show |
9 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1498-197C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647557 | |||||||
| chr14:49647642 | G | T | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1498-282C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647642 | |||||||
| chr14:49647860 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1498-500G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49647860 | |||||||
| chr14:49648008 | C | T | 1 | a0001c0002t0002g0153 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1498-648G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648008 | |||||||
| chr14:49648083 | T | G | 48 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(45): Show |
52 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.1498-723A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648083 | |||||||
| chr14:49648122 | C | A | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1498-762G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648122 | |||||||
| chr14:49648174 | A | G | 1 | a0001c0004t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1498-814T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648174 | |||||||
| chr14:49648228 | C | T | 11 | a0001c0002t0002g0003 a0001c0002t0002g0027 a0001c0002t0002g0033 others(8): Show |
13 | HG00597.hp1 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1498-868G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648228 | |||||||
| chr14:49648320 | G | A | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1498-960C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648320 | |||||||
| chr14:49648636 | C | T | 5 | a0001c0002t0002g0190 a0001c0003t0002g0057 a0001c0003t0002g0058 others(2): Show |
5 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498-1276G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648636 | |||||||
| chr14:49648731 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1498-1371G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648731 | |||||||
| chr14:49648881 | G | C | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1497+1384C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648881 | |||||||
| chr14:49648984 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1497+1281T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49648984 | |||||||
| chr14:49649022 | A | G | 3 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0179 |
3 | HG02559.hp1 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1497+1243T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649022 | |||||||
| chr14:49649137 | C | CT | 28 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0062 others(25): Show |
28 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.1497+1127dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649137 | |||||||
| chr14:49649137 | C | CTT | 7 | a0001c0001t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0028 others(4): Show |
7 | HG01358.hp1 HG01361.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1497+1126_1497+112 others(6): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649137 | |||||||
| chr14:49649137 | CTTT | C | 8 | a0001c0002t0002g0003 a0001c0002t0002g0027 a0001c0002t0002g0033 others(5): Show |
9 | HG02258.hp2 HG02630.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1497+1125_1497+112 others(7): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649137 | |||||||
| chr14:49649137 | CTTTT | C | 28 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(25): Show |
30 | HG00735.hp1 HG00741.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.1497+1124_1497+112 others(8): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649137 | |||||||
| chr14:49649137 | CTTTTT | C | 8 | a0001c0002t0002g0176 a0001c0002t0002g0190 a0001c0003t0002g0057 others(5): Show |
8 | HG01167.hp2 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1497+1123_1497+112 others(9): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649137 | |||||||
| chr14:49649302 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1497+963A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649302 | |||||||
| chr14:49649349 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG00642.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1497+916A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649349 | |||||||
| chr14:49649436 | A | G | 2 | a0001c0001t0001g0199 a0001c0002t0001g0005 |
3 | HG01361.hp2 HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1497+829T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649436 | |||||||
| chr14:49649438 | A | G | 1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1497+827T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649438 | |||||||
| chr14:49649453 | C | T | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1497+812G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649453 | |||||||
| chr14:49649597 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1497+668C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649597 | |||||||
| chr14:49649640 | G | A | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1497+625C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649640 | |||||||
| chr14:49649740 | T | C | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1497+525A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649740 | |||||||
| chr14:49649745 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1497+520C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649745 | |||||||
| chr14:49649985 | C | T | 1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1497+280G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49649985 | |||||||
| chr14:49650034 | G | T | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1497+231C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49650034 | |||||||
| chr14:49650144 | G | A | 39 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(36): Show |
41 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.1497+121C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49650144 | |||||||
| chr14:49650248 | A | G | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1497+17T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 17/18 | chr14 | 49650248 | |||||||
| chr14:49651070 | C | T | 70 | a0001c0001t0001g0036 a0001c0001t0001g0106 a0001c0001t0002g0006 others(67): Show |
76 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1320+199G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651070 | |||||||
| chr14:49651071 | TAA | T | 70 | a0001c0001t0001g0036 a0001c0001t0001g0106 a0001c0001t0002g0006 others(67): Show |
76 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1320+196_1320+197d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651071 | |||||||
| chr14:49651077 | A | C | 70 | a0001c0001t0001g0036 a0001c0001t0001g0106 a0001c0001t0002g0006 others(67): Show |
76 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1320+192T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651077 | |||||||
| chr14:49651087 | A | C | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1320+182T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651087 | |||||||
| chr14:49651119 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1320+150T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651119 | |||||||
| chr14:49651138 | C | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0212 |
2 | HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1320+131G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651138 | |||||||
| chr14:49651160 | T | C | 1 | a0001c0004t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1320+109A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651160 | |||||||
| chr14:49651233 | T | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0099 |
2 | HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1320+36A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 16/18 | chr14 | 49651233 | |||||||
| chr14:49651515 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1212-138G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49651515 | |||||||
| chr14:49651641 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1212-264T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49651641 | |||||||
| chr14:49651692 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1212-315T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49651692 | |||||||
| chr14:49651942 | G | A | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1212-565C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49651942 | |||||||
| chr14:49652058 | GGGGTCCC others(12): Show |
G | 1 | a0001c0001t0001g0083 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1212-700_1212-682d others(21): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652058 | |||||||
| chr14:49652112 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0064 |
6 | HG02559.hp2 HG02886.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1212-735C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652112 | |||||||
| chr14:49652123 | T | C | 20 | a0001c0001t0001g0036 a0001c0001t0001g0106 a0001c0002t0001g0004 others(17): Show |
22 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.1212-746A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652123 | |||||||
| chr14:49652152 | TAAGAATA others(150): Show |
T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0021 others(146): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1212-932_1212-776d others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652152 | |||||||
| chr14:49652165 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1212-788G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652165 | |||||||
| chr14:49652219 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0196 |
2 | HG02080.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1212-842C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652219 | |||||||
| chr14:49652263 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0085 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1212-896_1212-887d others(12): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0056 a0001c0001t0001g0212 |
2 | HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1212-898_1212-887d others(14): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0060 a0001c0001t0001g0162 |
2 | HG03927.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1212-899_1212-887d others(15): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0128 others(1): Show |
6 | HG00438.hp1 HG00438.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1212-897_1212-887d others(13): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0079 others(1): Show |
5 | HG00741.hp2 HG01346.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1212-898_1212-887d others(14): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0088 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1212-899_1212-887d others(15): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1212-900_1212-887d others(16): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0007 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1212-901_1212-887d others(17): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0070 |
2 | NA18979.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1212-902_1212-887d others(18): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(10): Show |
C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0084 others(3): Show |
6 | HG00597.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1212-903_1212-887d others(19): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(11): Show |
C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(10): Show |
15 | HG00544.hp2 HG00673.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1212-904_1212-887d others(20): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(12): Show |
C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0195 a0001c0001t0001g0202 |
3 | HG02040.hp1 HG02040.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1212-905_1212-887d others(21): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(17): Show |
C | 1 | a0001c0001t0001g0090 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1212-910_1212-887d others(26): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(18): Show |
C | 1 | a0001c0001t0001g0093 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1212-911_1212-887d others(27): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(20): Show |
C | 1 | a0001c0001t0001g0032 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1212-913_1212-887d others(29): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(22): Show |
C | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1212-915_1212-887d others(31): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652263 | CAAAAAAA others(26): Show |
C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0092 |
2 | HG00558.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.1212-919_1212-887d others(35): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652263 | |||||||
| chr14:49652311 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0193 |
2 | HG00621.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1212-934T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652311 | |||||||
| chr14:49652426 | G | A | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1212-1049C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652426 | |||||||
| chr14:49652646 | T | A | 5 | a0001c0002t0002g0190 a0001c0003t0002g0057 a0001c0003t0002g0058 others(2): Show |
5 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1212-1269A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652646 | |||||||
| chr14:49652747 | T | C | 30 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(27): Show |
32 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.1211+1243A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652747 | |||||||
| chr14:49652856 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1211+1134G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652856 | |||||||
| chr14:49652918 | G | C | 1 | a0001c0002t0002g0181 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1211+1072C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652918 | |||||||
| chr14:49652974 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1211+1016A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652974 | |||||||
| chr14:49652975 | T | C | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1211+1015A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49652975 | |||||||
| chr14:49653194 | G | T | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1211+796C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49653194 | |||||||
| chr14:49653431 | G | A | 50 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0076 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1211+559C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49653431 | |||||||
| chr14:49653565 | T | C | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1211+425A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49653565 | |||||||
| chr14:49653576 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1211+414T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 15/18 | chr14 | 49653576 | |||||||
| chr14:49654140 | C | T | 49 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(46): Show |
53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1133+15G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 14/18 | chr14 | 49654140 | |||||||
| chr14:49654318 | C | T | 2 | a0001c0002t0002g0031 a0001c0002t0002g0153 |
2 | HG01258.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1074-104G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 13/18 | chr14 | 49654318 | |||||||
| chr14:49654419 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1074-205A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 13/18 | chr14 | 49654419 | |||||||
| chr14:49654731 | G | GT | 11 | a0001c0001t0001g0036 a0001c0002t0002g0190 a0001c0003t0002g0057 others(8): Show |
11 | HG00597.hp1 HG02055.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1073+52dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 13/18 | chr14 | 49654731 | |||||||
| chr14:49655458 | A | AAC | 15 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0045 others(12): Show |
20 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.928+211_928+212dup others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | |||||||
| chr14:49655458 | A | AACAC | 3 | a0001c0001t0001g0116 a0001c0002t0002g0190 a0001c0003t0002g0188 |
3 | HG02055.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.928+209_928+212dup others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | |||||||
| chr14:49655458 | A | AACACAC | 8 | a0001c0002t0001g0005 a0001c0002t0002g0003 a0001c0002t0002g0027 others(5): Show |
11 | HG01361.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.928+207_928+212dup others(6): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | |||||||
| chr14:49655458 | A | AACACACA others(1): Show |
3 | a0001c0002t0001g0038 a0001c0002t0002g0033 a0001c0002t0002g0034 |
3 | HG02258.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.928+205_928+212dup others(8): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | |||||||
| chr14:49655458 | A | AACACACA others(3): Show |
2 | a0001c0002t0001g0044 a0001c0002t0001g0163 |
2 | HG01099.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.928+203_928+212dup others(10): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | |||||||
| chr14:49655458 | A | AACACACA others(5): Show |
10 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0035 others(7): Show |
10 | HG00733.hp2 HG02280.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.928+201_928+212dup others(12): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | |||||||
| chr14:49655458 | A | AACACACA others(7): Show |
4 | a0001c0002t0001g0004 a0001c0002t0001g0030 a0001c0002t0001g0041 others(1): Show |
5 | HG01358.hp1 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.928+199_928+212dup others(14): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | |||||||
| chr14:49655458 | A | AACACACA others(9): Show |
1 | a0001c0001t0001g0036 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.928+197_928+212dup others(16): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | |||||||
| chr14:49655458 | A | AC | 2 | a0001c0001t0001g0047 a0001c0001t0001g0113 |
2 | HG01261.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.928+212_928+213ins others(1): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | |||||||
| chr14:49655458 | AAC | A | 32 | a0001c0001t0001g0115 a0001c0001t0002g0006 a0001c0001t0002g0076 others(29): Show |
34 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.928+211_928+212del others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | |||||||
| chr14:49655458 | AACAC | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0072 a0001c0001t0001g0146 others(1): Show |
4 | HG00140.hp1 HG01099.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+209_928+212del others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655458 | |||||||
| chr14:49655468 | C | T | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.928+203G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655468 | |||||||
| chr14:49655540 | T | C | 36 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(33): Show |
38 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.928+131A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655540 | |||||||
| chr14:49655562 | C | CAG | 49 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(46): Show |
53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.928+108_928+109ins others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655562 | |||||||
| chr14:49655628 | C | A | 1 | a0001c0002t0002g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.928+43G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655628 | |||||||
| chr14:49655634 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.928+37T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 11/18 | chr14 | 49655634 | |||||||
| chr14:49656041 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0191 |
2 | NA19000.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.756-198A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656041 | |||||||
| chr14:49656051 | C | A | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.756-208G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656051 | |||||||
| chr14:49656078 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0142 |
3 | HG01361.hp1 HG01433.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.756-235C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656078 | |||||||
| chr14:49656223 | C | T | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.756-380G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656223 | |||||||
| chr14:49656281 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.756-438C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656281 | |||||||
| chr14:49656327 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.756-484T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656327 | |||||||
| chr14:49656354 | C | CA | 19 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0062 others(16): Show |
19 | HG00558.hp2 HG01081.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.756-512dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656354 | |||||||
| chr14:49656354 | CA | C | 51 | a0001c0001t0001g0050 a0001c0001t0001g0157 a0001c0001t0002g0006 others(48): Show |
55 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.756-512delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656354 | |||||||
| chr14:49656366 | A | C | 49 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(46): Show |
53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.756-523T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656366 | |||||||
| chr14:49656370 | A | G | 2 | a0003c0006t0002g0015 a0003c0008t0002g0213 |
2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.756-527T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656370 | |||||||
| chr14:49656430 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.756-587C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656430 | |||||||
| chr14:49656575 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.756-732A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656575 | |||||||
| chr14:49656759 | T | G | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.756-916A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49656759 | |||||||
| chr14:49657048 | G | C | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.756-1205C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657048 | |||||||
| chr14:49657107 | T | C | 49 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(46): Show |
53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.756-1264A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657107 | |||||||
| chr14:49657112 | C | CA | 32 | a0001c0001t0001g0008 a0001c0001t0001g0067 a0001c0001t0001g0070 others(29): Show |
34 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.756-1270dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657112 | |||||||
| chr14:49657112 | C | CAA | 37 | a0001c0001t0001g0112 a0001c0001t0002g0006 a0001c0001t0002g0076 others(34): Show |
41 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.756-1271_756-1270d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657112 | |||||||
| chr14:49657112 | CA | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0002t0002g0190 others(5): Show |
12 | HG02055.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.756-1270delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657112 | |||||||
| chr14:49657199 | G | A | 3 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0179 |
3 | HG02559.hp1 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.756-1356C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657199 | |||||||
| chr14:49657301 | T | A | 1 | a0001c0001t0001g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.756-1458A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657301 | |||||||
| chr14:49657405 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.756-1562A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657405 | |||||||
| chr14:49657429 | CT | C | 14 | a0001c0001t0001g0090 a0001c0001t0001g0106 a0001c0001t0001g0198 others(11): Show |
16 | HG00597.hp1 HG01891.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.756-1587delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657429 | |||||||
| chr14:49657455 | C | T | 1 | a0001c0004t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.756-1612G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657455 | |||||||
| chr14:49657503 | C | T | 1 | a0001c0002t0001g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.756-1660G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657503 | |||||||
| chr14:49657814 | T | C | 49 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(46): Show |
53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.756-1971A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49657814 | |||||||
| chr14:49658003 | C | A | 1 | a0001c0001t0001g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.756-2160G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658003 | |||||||
| chr14:49658076 | C | CT | 19 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0005 others(16): Show |
21 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.756-2234dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658076 | |||||||
| chr14:49658375 | C | G | 1 | a0001c0004t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.756-2532G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658375 | |||||||
| chr14:49658424 | G | A | 19 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0005 others(16): Show |
21 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.756-2581C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658424 | |||||||
| chr14:49658506 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.756-2663G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658506 | |||||||
| chr14:49658595 | G | A | 67 | a0001c0001t0001g0036 a0001c0001t0002g0006 a0001c0001t0002g0076 others(64): Show |
73 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.756-2752C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658595 | |||||||
| chr14:49658611 | G | A | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.756-2768C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49658611 | |||||||
| chr14:49659161 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.756-3318T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659161 | |||||||
| chr14:49659263 | A | AT | 68 | a0001c0001t0001g0036 a0001c0001t0002g0006 a0001c0001t0002g0076 others(65): Show |
74 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.756-3421dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659263 | |||||||
| chr14:49659302 | G | T | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.756-3459C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659302 | |||||||
| chr14:49659346 | G | A | 47 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(44): Show |
51 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.756-3503C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659346 | |||||||
| chr14:49659435 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(160): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.756-3592G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659435 | |||||||
| chr14:49659494 | A | G | 49 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(46): Show |
53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.756-3651T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659494 | |||||||
| chr14:49659654 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.755+3661G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659654 | |||||||
| chr14:49659723 | G | A | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.755+3592C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49659723 | |||||||
| chr14:49660176 | G | T | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.755+3139C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660176 | |||||||
| chr14:49660299 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0131 a0001c0001t0001g0132 |
4 | HG01496.hp2 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.755+3016G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660299 | |||||||
| chr14:49660326 | T | A | 6 | a0001c0002t0002g0190 a0001c0003t0002g0057 a0001c0003t0002g0058 others(3): Show |
6 | HG02055.hp1 HG02622.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.755+2989A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660326 | |||||||
| chr14:49660558 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.755+2757C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660558 | |||||||
| chr14:49660657 | C | T | 49 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(46): Show |
53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.755+2658G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660657 | |||||||
| chr14:49660712 | C | T | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.755+2603G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660712 | |||||||
| chr14:49660813 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.755+2502T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660813 | |||||||
| chr14:49660852 | T | C | 2 | a0003c0006t0002g0015 a0003c0008t0002g0213 |
2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.755+2463A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660852 | |||||||
| chr14:49660873 | A | G | 49 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(46): Show |
53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.755+2442T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660873 | |||||||
| chr14:49660886 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.755+2429G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660886 | |||||||
| chr14:49660925 | A | G | 1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.755+2390T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49660925 | |||||||
| chr14:49661141 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.755+2174C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661141 | |||||||
| chr14:49661177 | T | C | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.755+2138A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661177 | |||||||
| chr14:49661214 | CA | C | 49 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(46): Show |
53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.755+2100delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661214 | |||||||
| chr14:49661387 | G | A | 49 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(46): Show |
53 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.755+1928C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661387 | |||||||
| chr14:49661548 | G | A | 28 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(25): Show |
30 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.755+1767C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661548 | |||||||
| chr14:49661825 | C | A | 1 | a0001c0001t0001g0195 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.755+1490G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661825 | |||||||
| chr14:49661953 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.755+1362A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661953 | |||||||
| chr14:49661964 | C | A | 1 | a0001c0003t0002g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.755+1351G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661964 | |||||||
| chr14:49661970 | G | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0092 |
3 | HG00438.hp2 HG00558.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.755+1345C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49661970 | |||||||
| chr14:49662134 | T | G | 4 | a0001c0002t0002g0014 a0001c0002t0002g0206 a0001c0002t0002g0207 others(1): Show |
5 | HG02451.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.755+1181A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662134 | |||||||
| chr14:49662140 | T | C | 4 | a0001c0002t0002g0014 a0001c0002t0002g0206 a0001c0002t0002g0207 others(1): Show |
5 | HG02451.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.755+1175A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662140 | |||||||
| chr14:49662233 | A | C | 1 | a0004c0009t0002g0214 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.755+1082T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662233 | |||||||
| chr14:49662301 | C | T | 1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.755+1014G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662301 | |||||||
| chr14:49662311 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.755+1004C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662311 | |||||||
| chr14:49662333 | C | G | 1 | a0001c0001t0001g0023 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.755+982G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662333 | |||||||
| chr14:49662649 | G | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0204 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.755+666C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662649 | |||||||
| chr14:49662797 | A | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(132): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.755+518T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662797 | |||||||
| chr14:49662803 | A | G | 1 | a0001c0002t0002g0181 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.755+512T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662803 | |||||||
| chr14:49662830 | T | C | 68 | a0001c0001t0001g0036 a0001c0001t0002g0006 a0001c0001t0002g0076 others(65): Show |
74 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.755+485A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49662830 | |||||||
| chr14:49663128 | T | A | 2 | a0003c0006t0002g0015 a0003c0008t0002g0213 |
2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.755+187A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49663128 | |||||||
| chr14:49663223 | C | T | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG01168.hp1 HG01192.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.755+92G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 10/18 | chr14 | 49663223 | |||||||
| chr14:49663468 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.683-81A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49663468 | |||||||
| chr14:49663614 | T | C | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.683-227A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49663614 | |||||||
| chr14:49663766 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.683-379A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49663766 | |||||||
| chr14:49663803 | C | T | 7 | a0001c0002t0002g0003 a0001c0002t0002g0027 a0001c0002t0002g0171 others(4): Show |
9 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.683-416G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49663803 | |||||||
| chr14:49663961 | C | T | 4 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(1): Show |
4 | NA18979.hp2 NA18988.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-574G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49663961 | |||||||
| chr14:49663962 | G | A | 1 | a0001c0004t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.683-575C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49663962 | |||||||
| chr14:49664041 | GA | G | 48 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(45): Show |
52 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.682+584delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664041 | |||||||
| chr14:49664192 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.682+434T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664192 | |||||||
| chr14:49664193 | C | T | 1 | a0001c0004t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.682+433G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664193 | |||||||
| chr14:49664214 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.682+412A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664214 | |||||||
| chr14:49664218 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.682+408T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664218 | |||||||
| chr14:49664219 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.682+407A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664219 | |||||||
| chr14:49664360 | G | GA | 23 | a0001c0001t0001g0036 a0001c0001t0001g0112 a0001c0001t0001g0191 others(20): Show |
25 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.682+265dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 9/18 | chr14 | 49664360 | |||||||
| chr14:49664777 | C | G | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.634-103G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 8/18 | chr14 | 49664777 | |||||||
| chr14:49665010 | T | C | 42 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(39): Show |
45 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.633+97A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 8/18 | chr14 | 49665010 | |||||||
| chr14:49665214 | T | C | 22 | a0001c0002t0002g0014 a0001c0002t0002g0031 a0001c0002t0002g0048 others(19): Show |
23 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.577-51A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665214 | |||||||
| chr14:49665550 | A | G | 37 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(34): Show |
40 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.577-387T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665550 | |||||||
| chr14:49665644 | T | G | 5 | a0001c0002t0001g0004 a0001c0002t0001g0028 a0001c0002t0001g0029 others(2): Show |
6 | HG02809.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.577-481A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665644 | |||||||
| chr14:49665677 | G | GT | 10 | a0001c0001t0001g0054 a0001c0001t0001g0099 a0001c0001t0001g0127 others(7): Show |
10 | HG01891.hp1 HG01978.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-515dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665677 | |||||||
| chr14:49665821 | A | T | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.576+509T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665821 | |||||||
| chr14:49665822 | T | TA | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.576+507_576+508ins others(1): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665822 | |||||||
| chr14:49665831 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0133 others(1): Show |
6 | HG02257.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.576+499A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49665831 | |||||||
| chr14:49666185 | AT | A | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.576+144delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49666185 | |||||||
| chr14:49666231 | T | G | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.576+99A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49666231 | |||||||
| chr14:49666315 | T | C | 40 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(37): Show |
43 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.576+15A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 7/18 | chr14 | 49666315 | |||||||
| chr14:49666500 | T | C | 42 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(39): Show |
45 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.493-87A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49666500 | |||||||
| chr14:49666573 | T | C | 40 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(37): Show |
43 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.493-160A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49666573 | |||||||
| chr14:49666651 | G | C | 1 | a0003c0008t0002g0213 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.493-238C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49666651 | |||||||
| chr14:49666729 | GAA | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-318_493-317del others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49666729 | |||||||
| chr14:49666914 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG01433.hp1 HG01884.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-501A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49666914 | |||||||
| chr14:49667086 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.493-673C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667086 | |||||||
| chr14:49667142 | C | T | 11 | a0001c0002t0001g0004 a0001c0002t0001g0028 a0001c0002t0001g0029 others(8): Show |
12 | HG00733.hp2 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.493-729G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667142 | |||||||
| chr14:49667184 | C | CA | 8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0117 others(5): Show |
8 | HG00558.hp2 HG00621.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.493-772dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667184 | |||||||
| chr14:49667198 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.493-785T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667198 | |||||||
| chr14:49667487 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.493-1074A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667487 | |||||||
| chr14:49667552 | C | CT | 38 | a0001c0001t0001g0212 a0001c0002t0002g0003 a0001c0002t0002g0014 others(35): Show |
41 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.493-1140dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667552 | |||||||
| chr14:49667552 | C | CTT | 5 | a0001c0003t0002g0057 a0001c0003t0002g0058 a0001c0003t0002g0187 others(2): Show |
5 | HG02622.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-1141_493-1140d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667552 | |||||||
| chr14:49667843 | T | C | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.493-1430A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667843 | |||||||
| chr14:49667917 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0002g0073 |
2 | HG01515.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.493-1504A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667917 | |||||||
| chr14:49667994 | G | A | 1 | a0001c0002t0002g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.492+1530C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49667994 | |||||||
| chr14:49668154 | T | G | 1 | a0001c0004t0004g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.492+1370A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668154 | |||||||
| chr14:49668251 | CAG | C | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.492+1271_492+1272d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668251 | |||||||
| chr14:49668289 | G | A | 1 | a0001c0002t0002g0027 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.492+1235C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668289 | |||||||
| chr14:49668558 | A | T | 28 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0031 others(25): Show |
31 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.492+966T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668558 | |||||||
| chr14:49668855 | C | T | 2 | a0003c0006t0002g0015 a0003c0008t0002g0213 |
2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.492+669G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668855 | |||||||
| chr14:49668856 | A | G | 40 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(37): Show |
43 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.492+668T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668856 | |||||||
| chr14:49668958 | G | A | 1 | a0001c0004t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.492+566C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668958 | |||||||
| chr14:49668999 | A | G | 42 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(39): Show |
45 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.492+525T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49668999 | |||||||
| chr14:49669175 | T | C | 5 | a0001c0003t0002g0057 a0001c0003t0002g0058 a0001c0003t0002g0187 others(2): Show |
5 | HG02622.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+349A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49669175 | |||||||
| chr14:49669277 | G | T | 5 | a0001c0003t0002g0057 a0001c0003t0002g0058 a0001c0003t0002g0187 others(2): Show |
5 | HG02622.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+247C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49669277 | |||||||
| chr14:49669302 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.492+222G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49669302 | |||||||
| chr14:49669407 | T | G | 4 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0118 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+117A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 6/18 | chr14 | 49669407 | |||||||
| chr14:49669640 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0117 |
3 | HG00609.hp1 NA18993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.418-42A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669640 | |||||||
| chr14:49669667 | G | A | 2 | a0003c0006t0002g0015 a0003c0008t0002g0213 |
2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.418-69C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669667 | |||||||
| chr14:49669711 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.418-113A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669711 | |||||||
| chr14:49669781 | G | A | 42 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(39): Show |
45 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.418-183C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669781 | |||||||
| chr14:49669842 | C | G | 1 | a0001c0001t0001g0150 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.418-244G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669842 | |||||||
| chr14:49669858 | C | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0211 |
2 | HG00544.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.418-260G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669858 | |||||||
| chr14:49669882 | T | C | 1 | a0001c0002t0001g0043 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.418-284A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669882 | |||||||
| chr14:49669891 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.418-293C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49669891 | |||||||
| chr14:49670081 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.418-483G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670081 | |||||||
| chr14:49670304 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0118 |
2 | HG02976.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.418-706C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670304 | |||||||
| chr14:49670317 | C | CA | 26 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0049 others(23): Show |
27 | HG00609.hp1 HG00733.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.418-720dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | |||||||
| chr14:49670317 | C | CAA | 18 | a0001c0002t0001g0005 a0001c0002t0001g0154 a0001c0002t0001g0163 others(15): Show |
22 | HG01361.hp2 HG01515.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.418-721_418-720dup others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | |||||||
| chr14:49670317 | C | CAAA | 8 | a0001c0002t0002g0027 a0001c0002t0002g0031 a0001c0002t0002g0153 others(5): Show |
8 | HG00741.hp1 HG01258.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.418-722_418-720dup others(3): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | |||||||
| chr14:49670317 | C | CAAAAA | 6 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(3): Show |
6 | HG00735.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.418-724_418-720dup others(5): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | |||||||
| chr14:49670317 | C | CAAAAAAA | 5 | a0001c0001t0001g0036 a0001c0002t0001g0037 a0001c0002t0001g0039 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.418-726_418-720dup others(7): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | |||||||
| chr14:49670317 | CA | C | 10 | a0001c0001t0001g0021 a0001c0001t0001g0097 a0001c0001t0001g0098 others(7): Show |
10 | HG00099.hp1 HG00099.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.418-720delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | |||||||
| chr14:49670317 | CAAAAAAA | C | 9 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0094 others(6): Show |
9 | HG00639.hp1 HG00642.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.418-726_418-720del others(7): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | |||||||
| chr14:49670317 | CAAAAAAA others(1): Show |
C | 49 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(46): Show |
55 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.418-727_418-720del others(8): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | |||||||
| chr14:49670317 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0002g0176 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.418-729_418-720del others(10): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | |||||||
| chr14:49670317 | CAAAAAAA others(4): Show |
C | 4 | a0001c0004t0004g0026 a0002c0005t0002g0017 a0003c0006t0002g0015 others(1): Show |
4 | HG00597.hp1 HG02615.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.418-730_418-720del others(11): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | |||||||
| chr14:49670317 | CAAAAAAA others(5): Show |
C | 1 | a0001c0004t0004g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.418-731_418-720del others(12): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670317 | |||||||
| chr14:49670447 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.418-849C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670447 | |||||||
| chr14:49670579 | A | G | 1 | a0002c0005t0002g0016 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.418-981T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670579 | |||||||
| chr14:49670662 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.418-1064C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670662 | |||||||
| chr14:49670706 | A | G | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.418-1108T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670706 | |||||||
| chr14:49670774 | G | C | 40 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(37): Show |
43 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.418-1176C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670774 | |||||||
| chr14:49670982 | T | G | 1 | a0001c0001t0001g0025 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.418-1384A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49670982 | |||||||
| chr14:49671230 | T | C | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.418-1632A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671230 | |||||||
| chr14:49671296 | C | A | 1 | a0001c0002t0002g0027 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.418-1698G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671296 | |||||||
| chr14:49671339 | T | C | 40 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(37): Show |
43 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.418-1741A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671339 | |||||||
| chr14:49671390 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.418-1792C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671390 | |||||||
| chr14:49671514 | G | T | 1 | a0001c0002t0002g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.418-1916C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671514 | |||||||
| chr14:49671536 | G | C | 1 | a0001c0002t0002g0027 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.418-1938C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671536 | |||||||
| chr14:49671618 | G | GA | 19 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0066 others(16): Show |
19 | HG00597.hp1 HG00621.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.418-2021dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671618 | |||||||
| chr14:49671618 | G | GAA | 27 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0031 others(24): Show |
30 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.418-2022_418-2021d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671618 | |||||||
| chr14:49671618 | G | GAAA | 10 | a0001c0002t0001g0041 a0001c0002t0002g0033 a0001c0002t0002g0034 others(7): Show |
10 | HG01358.hp1 HG01891.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.418-2023_418-2021d others(5): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671618 | |||||||
| chr14:49671692 | T | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0200 |
2 | HG00438.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.418-2094A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671692 | |||||||
| chr14:49671784 | G | A | 8 | a0001c0002t0002g0003 a0001c0002t0002g0171 a0001c0002t0002g0172 others(5): Show |
10 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.418-2186C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49671784 | |||||||
| chr14:49672040 | T | C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0143 others(1): Show |
4 | HG00621.hp2 HG00673.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.417+2083A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672040 | |||||||
| chr14:49672077 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(5): Show |
12 | HG01496.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.417+2046C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672077 | |||||||
| chr14:49672253 | T | G | 1 | a0001c0001t0002g0078 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.417+1870A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672253 | |||||||
| chr14:49672284 | A | G | 42 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(39): Show |
45 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.417+1839T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672284 | |||||||
| chr14:49672396 | CTTTA | C | 36 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(33): Show |
39 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.417+1723_417+1726d others(6): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672396 | |||||||
| chr14:49672402 | T | C | 20 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0005 others(17): Show |
22 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.417+1721A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672402 | |||||||
| chr14:49672501 | CT | C | 39 | a0001c0001t0001g0135 a0001c0002t0002g0003 a0001c0002t0002g0014 others(36): Show |
42 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.417+1621delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672501 | |||||||
| chr14:49672585 | C | T | 4 | a0001c0001t0002g0006 a0001c0001t0002g0076 a0001c0001t0002g0077 others(1): Show |
5 | HG01258.hp2 HG01978.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.417+1538G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672585 | |||||||
| chr14:49672801 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.417+1322G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672801 | |||||||
| chr14:49672923 | T | C | 1 | a0001c0002t0002g0027 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.417+1200A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672923 | |||||||
| chr14:49672996 | C | T | 1 | a0003c0006t0002g0015 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.417+1127G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49672996 | |||||||
| chr14:49673122 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.417+1001A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673122 | |||||||
| chr14:49673564 | T | C | 2 | a0003c0006t0002g0015 a0003c0008t0002g0213 |
2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.417+559A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673564 | |||||||
| chr14:49673569 | A | G | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.417+554T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673569 | |||||||
| chr14:49673671 | G | A | 36 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(33): Show |
39 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.417+452C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673671 | |||||||
| chr14:49673671 | G | C | 3 | a0001c0003t0002g0187 a0001c0003t0002g0188 a0005c0007t0002g0189 |
3 | HG02970.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.417+452C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673671 | |||||||
| chr14:49673695 | G | A | 37 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(34): Show |
40 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.417+428C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673695 | |||||||
| chr14:49673740 | G | A | 3 | a0001c0002t0002g0190 a0003c0006t0002g0015 a0003c0008t0002g0213 |
3 | HG02055.hp1 HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.417+383C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 5/18 | chr14 | 49673740 | |||||||
| chr14:49674510 | A | C | 4 | a0001c0004t0004g0026 a0001c0004t0004g0186 a0002c0005t0002g0016 others(1): Show |
4 | HG00597.hp1 HG03098.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.246-83T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49674510 | |||||||
| chr14:49674540 | C | G | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.246-113G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49674540 | |||||||
| chr14:49674606 | C | G | 60 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0005 others(57): Show |
65 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.246-179G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49674606 | |||||||
| chr14:49674607 | T | C | 60 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0005 others(57): Show |
65 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.246-180A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49674607 | |||||||
| chr14:49674730 | T | C | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.246-303A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49674730 | |||||||
| chr14:49674900 | G | A | 19 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0005 others(16): Show |
21 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.246-473C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49674900 | |||||||
| chr14:49675088 | A | AT | 56 | a0001c0001t0001g0036 a0001c0001t0001g0074 a0001c0002t0001g0004 others(53): Show |
61 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.246-662dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675088 | |||||||
| chr14:49675098 | T | TC | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.246-672_246-671ins others(1): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675098 | |||||||
| chr14:49675171 | G | A | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG00280.hp2 HG01074.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-744C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675171 | |||||||
| chr14:49675242 | G | A | 3 | a0001c0003t0002g0187 a0001c0003t0002g0188 a0005c0007t0002g0189 |
3 | HG02970.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.246-815C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675242 | |||||||
| chr14:49675363 | C | A | 2 | a0003c0006t0002g0015 a0003c0008t0002g0213 |
2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.246-936G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675363 | |||||||
| chr14:49675462 | GAC | G | 2 | a0001c0004t0004g0026 a0001c0004t0004g0186 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.246-1037_246-1036d others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675462 | |||||||
| chr14:49675519 | C | T | 56 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0005 others(53): Show |
61 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.246-1092G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675519 | |||||||
| chr14:49675636 | G | A | 56 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0005 others(53): Show |
61 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.246-1209C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675636 | |||||||
| chr14:49675668 | C | T | 3 | a0001c0003t0002g0187 a0001c0003t0002g0188 a0005c0007t0002g0189 |
3 | HG02970.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.246-1241G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675668 | |||||||
| chr14:49675669 | G | A | 2 | a0001c0002t0003g0169 a0001c0002t0003g0183 |
2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.246-1242C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49675669 | |||||||
| chr14:49676074 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.246-1647C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676074 | |||||||
| chr14:49676085 | A | G | 2 | a0001c0003t0002g0187 a0001c0003t0002g0188 |
2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.246-1658T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676085 | |||||||
| chr14:49676163 | T | C | 2 | a0001c0002t0001g0029 a0001c0002t0001g0030 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.246-1736A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676163 | |||||||
| chr14:49676255 | C | T | 60 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0005 others(57): Show |
65 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.246-1828G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676255 | |||||||
| chr14:49676495 | C | T | 60 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0005 others(57): Show |
65 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.246-2068G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676495 | |||||||
| chr14:49676500 | G | T | 1 | a0004c0009t0002g0214 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.246-2073C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676500 | |||||||
| chr14:49676540 | T | C | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.246-2113A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676540 | |||||||
| chr14:49676685 | G | C | 1 | a0001c0002t0001g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.246-2258C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676685 | |||||||
| chr14:49676761 | A | G | 60 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0005 others(57): Show |
65 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.246-2334T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676761 | |||||||
| chr14:49676785 | T | G | 60 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0005 others(57): Show |
65 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.246-2358A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676785 | |||||||
| chr14:49676945 | A | G | 1 | a0001c0002t0002g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.246-2518T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676945 | |||||||
| chr14:49676971 | G | A | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.246-2544C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49676971 | |||||||
| chr14:49677014 | G | T | 2 | a0001c0003t0002g0187 a0001c0003t0002g0188 |
2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.246-2587C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677014 | |||||||
| chr14:49677082 | G | C | 3 | a0001c0001t0001g0202 a0002c0005t0002g0016 a0002c0005t0002g0017 |
3 | HG00597.hp1 HG02040.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.245+2643C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677082 | |||||||
| chr14:49677100 | C | T | 1 | a0001c0002t0001g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.245+2625G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677100 | |||||||
| chr14:49677241 | G | T | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.245+2484C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677241 | |||||||
| chr14:49677248 | G | A | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.245+2477C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677248 | |||||||
| chr14:49677325 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.245+2400C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677325 | |||||||
| chr14:49677335 | T | C | 52 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0028 others(49): Show |
56 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.245+2390A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677335 | |||||||
| chr14:49677535 | G | A | 1 | a0001c0001t0001g0013 | 2 | NA18961.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.245+2190C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677535 | |||||||
| chr14:49677547 | G | A | 2 | a0003c0006t0002g0015 a0003c0008t0002g0213 |
2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.245+2178C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677547 | |||||||
| chr14:49677615 | G | A | 1 | a0001c0004t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245+2110C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677615 | |||||||
| chr14:49677755 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.245+1970C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677755 | |||||||
| chr14:49677927 | T | C | 2 | a0003c0006t0002g0015 a0003c0008t0002g0213 |
2 | HG02615.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.245+1798A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677927 | |||||||
| chr14:49677980 | CTTTATTT others(7): Show |
C | 2 | a0001c0001t0001g0072 a0001c0001t0002g0073 |
2 | HG01515.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.245+1731_245+1744d others(16): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677980 | |||||||
| chr14:49677998 | AT | A | 29 | a0001c0002t0002g0014 a0001c0002t0002g0031 a0001c0002t0002g0033 others(26): Show |
30 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.245+1726delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49677998 | |||||||
| chr14:49678000 | TTTA | T | 21 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0028 others(18): Show |
22 | HG00597.hp1 HG00733.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.245+1722_245+1724d others(5): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678000 | |||||||
| chr14:49678002 | T | A | 9 | a0001c0002t0001g0005 a0001c0002t0002g0003 a0001c0002t0002g0171 others(6): Show |
12 | HG01361.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.245+1723A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678002 | |||||||
| chr14:49678003 | A | T | 10 | a0001c0002t0001g0005 a0001c0002t0002g0003 a0001c0002t0002g0027 others(7): Show |
13 | HG01361.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.245+1722T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678003 | |||||||
| chr14:49678005 | T | A | 20 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0028 others(17): Show |
21 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.245+1720A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678005 | |||||||
| chr14:49678007 | T | A | 4 | a0001c0003t0002g0187 a0001c0003t0002g0188 a0001c0004t0004g0186 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.245+1718A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678007 | |||||||
| chr14:49678063 | G | A | 3 | a0001c0002t0002g0190 a0002c0005t0002g0016 a0002c0005t0002g0017 |
3 | HG00597.hp1 HG02055.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.245+1662C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678063 | |||||||
| chr14:49678133 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.245+1592C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678133 | |||||||
| chr14:49678294 | C | T | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.245+1431G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678294 | |||||||
| chr14:49678339 | G | A | 7 | a0001c0001t0001g0053 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.245+1386C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678339 | |||||||
| chr14:49678397 | C | G | 21 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0028 others(18): Show |
22 | HG00597.hp1 HG00733.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.245+1328G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678397 | |||||||
| chr14:49678409 | T | A | 1 | a0001c0001t0001g0160 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.245+1316A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678409 | |||||||
| chr14:49678410 | G | T | 1 | a0001c0002t0002g0027 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.245+1315C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678410 | |||||||
| chr14:49678488 | T | A | 1 | a0001c0001t0001g0160 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.245+1237A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678488 | |||||||
| chr14:49678619 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.245+1106A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678619 | |||||||
| chr14:49678703 | C | T | 3 | a0001c0003t0002g0187 a0001c0003t0002g0188 a0005c0007t0002g0189 |
3 | HG02970.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.245+1022G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678703 | |||||||
| chr14:49678803 | C | T | 20 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0028 others(17): Show |
21 | HG00597.hp1 HG00733.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.245+922G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678803 | |||||||
| chr14:49678846 | T | TG | 57 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0005 others(54): Show |
62 | HG00597.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.245+878dupC | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678846 | |||||||
| chr14:49678953 | G | A | 1 | a0001c0002t0002g0027 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.245+772C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678953 | |||||||
| chr14:49678963 | T | C | 7 | a0001c0001t0001g0053 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.245+762A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49678963 | |||||||
| chr14:49679186 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0191 |
3 | NA18979.hp2 NA19000.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.245+539G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49679186 | |||||||
| chr14:49679190 | CA | C | 18 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0028 others(15): Show |
19 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.245+534delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49679190 | |||||||
| chr14:49679413 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.245+312T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49679413 | |||||||
| chr14:49679425 | A | T | 1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.245+300T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49679425 | |||||||
| chr14:49679470 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.245+255C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49679470 | |||||||
| chr14:49679680 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.245+45G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 3/18 | chr14 | 49679680 | |||||||
| chr14:49679806 | A | G | 4 | a0001c0003t0002g0187 a0001c0003t0002g0188 a0001c0004t0004g0186 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.170-6T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49679806 | |||||||
| chr14:49679835 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.170-35G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49679835 | |||||||
| chr14:49679835 | C | CA | 21 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0028 others(18): Show |
22 | HG00597.hp1 HG00733.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.170-36dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49679835 | |||||||
| chr14:49679839 | A | C | 1 | a0001c0002t0002g0027 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.170-39T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49679839 | |||||||
| chr14:49680003 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.170-203T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680003 | |||||||
| chr14:49680142 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.170-342C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680142 | |||||||
| chr14:49680353 | C | CA | 63 | a0001c0001t0001g0036 a0001c0001t0001g0152 a0001c0001t0001g0160 others(60): Show |
68 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.170-554dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680353 | |||||||
| chr14:49680639 | GA | G | 4 | a0001c0003t0002g0187 a0001c0003t0002g0188 a0001c0004t0004g0186 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-840delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680639 | |||||||
| chr14:49680690 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.170-890C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680690 | |||||||
| chr14:49680822 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.170-1022C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680822 | |||||||
| chr14:49680852 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.170-1052G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680852 | |||||||
| chr14:49680900 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.170-1100G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49680900 | |||||||
| chr14:49681140 | T | C | 1 | a0001c0002t0001g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.170-1340A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681140 | |||||||
| chr14:49681156 | C | T | 4 | a0001c0003t0002g0187 a0001c0003t0002g0188 a0001c0004t0004g0186 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-1356G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681156 | |||||||
| chr14:49681260 | C | A | 3 | a0001c0004t0004g0026 a0002c0005t0002g0016 a0002c0005t0002g0017 |
3 | HG00597.hp1 HG03098.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.170-1460G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681260 | |||||||
| chr14:49681458 | C | A | 3 | a0001c0004t0004g0026 a0002c0005t0002g0016 a0002c0005t0002g0017 |
3 | HG00597.hp1 HG03098.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.170-1658G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681458 | |||||||
| chr14:49681526 | C | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.170-1726G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681526 | |||||||
| chr14:49681723 | AAGATGGC others(17): Show |
A | 1 | a0001c0001t0001g0164 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.169+1846_169+1869d others(26): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681723 | |||||||
| chr14:49681730 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.169+1863G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681730 | |||||||
| chr14:49681755 | G | A | 1 | a0001c0004t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169+1838C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681755 | |||||||
| chr14:49681776 | G | A | 1 | a0001c0002t0002g0184 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.169+1817C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681776 | |||||||
| chr14:49681830 | C | CA | 8 | a0001c0001t0001g0052 a0001c0001t0001g0159 a0001c0001t0001g0160 others(5): Show |
8 | HG00642.hp2 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+1762dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681830 | |||||||
| chr14:49681830 | CA | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
9 | HG02559.hp2 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.169+1762delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681830 | |||||||
| chr14:49681878 | C | G | 3 | a0001c0004t0004g0026 a0002c0005t0002g0016 a0002c0005t0002g0017 |
3 | HG00597.hp1 HG03098.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.169+1715G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681878 | |||||||
| chr14:49681951 | A | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG01433.hp1 HG01884.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+1642T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49681951 | |||||||
| chr14:49682004 | C | CT | 7 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0060 others(4): Show |
7 | HG00741.hp2 HG01099.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+1588dupA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682004 | |||||||
| chr14:49682004 | CT | C | 5 | a0001c0002t0002g0185 a0001c0002t0002g0190 a0001c0003t0002g0187 others(2): Show |
5 | HG01943.hp2 HG02055.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+1588delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682004 | |||||||
| chr14:49682161 | T | C | 16 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0028 others(13): Show |
17 | HG01099.hp1 HG01358.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+1432A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682161 | |||||||
| chr14:49682367 | A | G | 59 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(56): Show |
64 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.169+1226T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682367 | |||||||
| chr14:49682443 | C | T | 4 | a0001c0003t0002g0187 a0001c0003t0002g0188 a0001c0004t0004g0186 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+1150G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682443 | |||||||
| chr14:49682530 | G | A | 4 | a0001c0003t0002g0187 a0001c0003t0002g0188 a0001c0004t0004g0186 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+1063C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682530 | |||||||
| chr14:49682569 | A | G | 50 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0028 others(47): Show |
54 | HG00597.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.169+1024T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682569 | |||||||
| chr14:49682572 | G | T | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1021C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682572 | |||||||
| chr14:49682573 | G | T | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1020C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682573 | |||||||
| chr14:49682576 | G | T | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1017C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682576 | |||||||
| chr14:49682577 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1016G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682577 | |||||||
| chr14:49682578 | A | T | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1015T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682578 | |||||||
| chr14:49682579 | G | C | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1014C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682579 | |||||||
| chr14:49682581 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1012C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682581 | |||||||
| chr14:49682582 | A | T | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1011T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682582 | |||||||
| chr14:49682583 | G | T | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1010C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682583 | |||||||
| chr14:49682584 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1009G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682584 | |||||||
| chr14:49682586 | G | C | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1007C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682586 | |||||||
| chr14:49682588 | A | T | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1005T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682588 | |||||||
| chr14:49682589 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1003_169+1004i others(16): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682589 | |||||||
| chr14:49682591 | A | T | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+1002T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682591 | |||||||
| chr14:49682599 | T | G | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+994A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682599 | |||||||
| chr14:49682600 | G | C | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+993C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682600 | |||||||
| chr14:49682601 | C | A | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+992G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682601 | |||||||
| chr14:49682615 | C | T | 1 | a0001c0002t0001g0044 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.169+978G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682615 | |||||||
| chr14:49682640 | G | GA | 43 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(40): Show |
45 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.169+952dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | |||||||
| chr14:49682640 | G | GAAAAAAA others(7): Show |
1 | a0001c0002t0002g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.169+939_169+952dup others(14): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | |||||||
| chr14:49682640 | G | GAAAAAAA others(8): Show |
3 | a0001c0002t0002g0003 a0001c0002t0002g0171 a0001c0002t0002g0182 |
4 | HG01891.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+938_169+952dup others(15): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | |||||||
| chr14:49682640 | G | GAAAAAAA others(9): Show |
4 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0002g0174 others(1): Show |
4 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+937_169+952dup others(16): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | |||||||
| chr14:49682640 | G | GAAAAAAA others(10): Show |
2 | a0001c0002t0002g0207 a0001c0002t0002g0208 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.169+936_169+952dup others(17): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | |||||||
| chr14:49682640 | G | GAAAAAAA others(11): Show |
2 | a0001c0002t0002g0014 a0004c0009t0002g0214 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.169+935_169+952dup others(18): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | |||||||
| chr14:49682640 | G | GAAAAAAA others(12): Show |
1 | a0001c0002t0002g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.169+934_169+952dup others(19): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | |||||||
| chr14:49682640 | G | GAAAAAAA others(14): Show |
1 | a0001c0002t0002g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.169+932_169+952dup others(21): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | |||||||
| chr14:49682640 | G | GGAAAAAA others(5): Show |
1 | a0001c0002t0002g0033 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.169+952_169+953ins others(12): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | |||||||
| chr14:49682640 | G | GGAAAAAA others(9): Show |
1 | a0001c0002t0002g0034 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.169+952_169+953ins others(16): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | |||||||
| chr14:49682640 | GA | G | 10 | a0001c0001t0001g0067 a0001c0001t0001g0102 a0001c0002t0002g0048 others(7): Show |
10 | HG01167.hp2 HG01515.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+952delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | |||||||
| chr14:49682640 | GAAA | G | 14 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0028 others(11): Show |
15 | HG01099.hp1 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.169+950_169+952del others(3): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | |||||||
| chr14:49682640 | GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0001g0198 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.169+942_169+952del others(11): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682640 | |||||||
| chr14:49682644 | A | G | 14 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0028 others(11): Show |
15 | HG01099.hp1 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.169+949T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682644 | |||||||
| chr14:49682645 | A | G | 14 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0028 others(11): Show |
15 | HG01099.hp1 HG01358.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.169+948T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682645 | |||||||
| chr14:49682691 | A | T | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+902T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682691 | |||||||
| chr14:49682694 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0056 |
2 | HG03490.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.169+899T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682694 | |||||||
| chr14:49682723 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+870A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682723 | |||||||
| chr14:49682725 | A | T | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+868T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682725 | |||||||
| chr14:49682727 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+866A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682727 | |||||||
| chr14:49682749 | C | A | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+844G>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682749 | |||||||
| chr14:49682826 | TA | T | 20 | a0001c0001t0001g0036 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
21 | HG01099.hp1 HG01099.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.169+766delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682826 | |||||||
| chr14:49682843 | T | G | 1 | a0001c0001t0001g0162 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.169+750A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682843 | |||||||
| chr14:49682873 | T | C | 3 | a0001c0004t0004g0026 a0002c0005t0002g0016 a0002c0005t0002g0017 |
3 | HG00597.hp1 HG03098.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.169+720A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682873 | |||||||
| chr14:49682965 | C | T | 1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169+628G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682965 | |||||||
| chr14:49682988 | G | C | 1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169+605C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682988 | |||||||
| chr14:49682989 | A | C | 1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169+604T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682989 | |||||||
| chr14:49682990 | A | AAATTGGG others(166): Show |
1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169+602_169+603ins others(173): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682990 | |||||||
| chr14:49682991 | G | C | 1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169+602C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682991 | |||||||
| chr14:49682992 | C | T | 1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169+601G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49682992 | |||||||
| chr14:49683009 | G | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 |
3 | HG00280.hp1 HG00642.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.169+584C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49683009 | |||||||
| chr14:49683030 | G | A | 4 | a0001c0003t0002g0187 a0001c0003t0002g0188 a0001c0004t0004g0186 others(1): Show |
4 | HG02970.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+563C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49683030 | |||||||
| chr14:49683305 | G | A | 1 | a0001c0002t0001g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169+288C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 2/18 | chr14 | 49683305 | |||||||
| chr14:49683803 | C | T | 1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.69-110G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49683803 | |||||||
| chr14:49683859 | T | A | 1 | a0001c0001t0001g0164 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.69-166A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49683859 | |||||||
| chr14:49683999 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.69-306T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49683999 | |||||||
| chr14:49684234 | G | A | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.69-541C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684234 | |||||||
| chr14:49684373 | G | A | 26 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0048 others(23): Show |
29 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.69-680C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684373 | |||||||
| chr14:49684410 | A | C | 26 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0048 others(23): Show |
29 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.69-717T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684410 | |||||||
| chr14:49684422 | G | A | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG00642.hp1 HG01168.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.69-729C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684422 | |||||||
| chr14:49684473 | A | G | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.69-780T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684473 | |||||||
| chr14:49684490 | T | G | 31 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0027 others(28): Show |
34 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.69-797A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684490 | |||||||
| chr14:49684623 | A | C | 1 | a0001c0001t0001g0045 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.69-930T>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684623 | |||||||
| chr14:49684661 | T | TA | 18 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(15): Show |
18 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.69-969dupT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684661 | |||||||
| chr14:49684661 | TA | T | 10 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0046 others(7): Show |
10 | HG00558.hp1 HG01099.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-969delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684661 | |||||||
| chr14:49684745 | G | C | 1 | a0001c0001t0001g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.69-1052C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684745 | |||||||
| chr14:49684765 | A | T | 1 | a0001c0002t0001g0005 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.69-1072T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49684765 | |||||||
| chr14:49685657 | T | C | 1 | a0001c0002t0002g0209 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69-1964A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685657 | |||||||
| chr14:49685715 | T | A | 1 | a0001c0002t0001g0044 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.69-2022A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685715 | |||||||
| chr14:49685789 | G | GTTTT | 19 | a0001c0001t0001g0036 a0001c0002t0001g0004 a0001c0002t0001g0028 others(16): Show |
20 | HG00597.hp1 HG01099.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.69-2100_69-2097dup others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685789 | |||||||
| chr14:49685790 | T | G | 1 | a0001c0002t0002g0027 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.69-2097A>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685790 | |||||||
| chr14:49685876 | C | T | 1 | a0001c0004t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.69-2183G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685876 | |||||||
| chr14:49685897 | G | T | 1 | a0001c0001t0001g0032 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.69-2204C>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685897 | |||||||
| chr14:49685964 | CT | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 |
3 | HG02622.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.68+2171delA | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49685964 | |||||||
| chr14:49686017 | C | T | 1 | a0001c0002t0002g0031 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.68+2119G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686017 | |||||||
| chr14:49686043 | C | T | 3 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 |
3 | HG02809.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.68+2093G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686043 | |||||||
| chr14:49686448 | A | G | 1 | a0001c0002t0002g0027 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.68+1688T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686448 | |||||||
| chr14:49686501 | A | G | 1 | a0001c0004t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.68+1635T>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686501 | |||||||
| chr14:49686526 | G | A | 1 | a0001c0002t0001g0205 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.68+1610C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686526 | |||||||
| chr14:49686543 | A | T | 1 | a0001c0001t0001g0025 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.68+1593T>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686543 | |||||||
| chr14:49686855 | C | G | 1 | a0001c0001t0001g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68+1281G>C | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686855 | |||||||
| chr14:49686871 | GCA | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 |
3 | HG02622.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.68+1263_68+1264del others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686871 | |||||||
| chr14:49686983 | T | A | 1 | a0004c0009t0002g0214 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.68+1153A>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686983 | |||||||
| chr14:49686985 | T | C | 5 | a0001c0002t0002g0014 a0001c0002t0002g0206 a0001c0002t0002g0207 others(2): Show |
6 | HG02451.hp1 HG02723.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+1151A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49686985 | |||||||
| chr14:49687158 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.68+978C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687158 | |||||||
| chr14:49687191 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.68+945C>T | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687191 | |||||||
| chr14:49687257 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.68+879A>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687257 | |||||||
| chr14:49687278 | C | CAT | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG00438.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.68+856_68+857dupAT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687278 | |||||||
| chr14:49687292 | C | T | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.68+844G>A | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687292 | |||||||
| chr14:49687295 | ACACAC | A | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.68+836_68+840delGT others(3): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687295 | |||||||
| chr14:49687300 | C | CCA | 30 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(27): Show |
30 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.68+834_68+835dupTG | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | |||||||
| chr14:49687300 | C | CCACA | 3 | a0001c0001t0001g0013 a0001c0001t0002g0006 a0001c0003t0002g0187 |
3 | HG01258.hp2 HG02970.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.68+832_68+835dupTG others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | |||||||
| chr14:49687300 | C | CCACACA | 11 | a0001c0001t0001g0011 a0001c0002t0002g0176 a0001c0002t0002g0177 others(8): Show |
11 | HG00735.hp1 HG01167.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+830_68+835dupTG others(4): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | |||||||
| chr14:49687300 | C | CCACACAC others(1): Show |
4 | a0001c0002t0002g0048 a0001c0002t0002g0180 a0001c0002t0002g0184 others(1): Show |
4 | HG01515.hp2 HG01978.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+828_68+835dupTG others(6): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | |||||||
| chr14:49687300 | CCA | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(42): Show |
49 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.68+834_68+835delTG | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | |||||||
| chr14:49687300 | CCACA | C | 24 | a0001c0001t0001g0009 a0001c0001t0001g0059 a0001c0001t0001g0065 others(21): Show |
26 | HG01361.hp2 HG01981.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.68+832_68+835delTG others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | |||||||
| chr14:49687300 | CCACACAC others(9): Show |
C | 2 | a0001c0003t0002g0057 a0001c0003t0002g0058 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.68+820_68+835delTG others(14): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687300 | |||||||
| chr14:49687307 | CA | C | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.68+828delT | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687307 | |||||||
| chr14:49687572 | G | C | 1 | a0003c0008t0002g0213 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.68+564C>G | POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687572 | |||||||
| chr14:49687727 | GTCTC | G | 2 | a0002c0005t0002g0016 a0002c0005t0002g0017 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.68+405_68+408delGA others(2): Show |
POLE2 | ENSG00000100479.14 | transcript | ENST00000216367.10 | protein_coding | 1/18 | chr14 | 49687727 |