Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7444 |
| ensemblid | ENSG00000028116.18 |
| hgncid | 12719 |
| symbol | VRK2 |
| name | VRK serine/threonine kinase 2 |
| refseq_nuc | NM_006296.7 |
| refseq_prot | NP_006287.2 |
| ensembl_nuc | ENST00000340157.9 |
| ensembl_prot | ENSP00000342381.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 58046806 |
| end | 58159871 |
| strand | + |
| ver | v1.2 |
| region | chr2:58046806-58159871 |
| region5000 | chr2:58041806-58164871 |
| regionname0 | VRK2_chr2_58046806_58159871 |
| regionname5000 | VRK2_chr2_58041806_58164871 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 508 | 242 | 76 | 42 | 91 | 11 | 21 | 66 | VRK2_chr2_58041806_58164871 | VRK2 | MPPKR others(503): Show |
chr2 | 58041806 | 58164871 |
| a0002 | 0/1 | 508 | 91 | 8 | 24 | 43 | 3 | 12 | 29 | VRK2_chr2_58041806_58164871 | VRK2 | MPPKR others(503): Show |
chr2 | 58041806 | 58164871 |
| a0003 | 0/0 | 508 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | MPPKR others(503): Show |
chr2 | 58041806 | 58164871 |
| a0004 | 0/0 | 508 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | MPPKR others(503): Show |
chr2 | 58041806 | 58164871 |
| a0005 | 0/0 | 508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | MPPKR others(503): Show |
chr2 | 58041806 | 58164871 |
| a0006 | 0/0 | 508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | MPPKR others(503): Show |
chr2 | 58041806 | 58164871 |
| a0007 | 0/0 | 508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | MPPKR others(503): Show |
chr2 | 58041806 | 58164871 |
| a0008 | 0/0 | 508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | MPPKR others(503): Show |
chr2 | 58041806 | 58164871 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1524 | 221 | 58 | 39 | 91 | 11 | 21 | VRK2_chr2_58041806_58164871 | VRK2 | ATGCC others(1519): Show |
chr2 | 58041806 | 58164871 | ||
| a0001c0003 | 0/0 | 1524 | 18 | 18 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | ATGCC others(1519): Show |
chr2 | 58041806 | 58164871 | ||
| a0001c0004 | 0/0 | 1524 | 3 | 0 | 3 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | ATGCC others(1519): Show |
chr2 | 58041806 | 58164871 | ||
| a0002c0002 | 0/1 | 1524 | 91 | 8 | 24 | 43 | 3 | 12 | VRK2_chr2_58041806_58164871 | VRK2 | ATGCC others(1519): Show |
chr2 | 58041806 | 58164871 | ||
| a0003c0005 | 0/0 | 1524 | 2 | 2 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | ATGCC others(1519): Show |
chr2 | 58041806 | 58164871 | ||
| a0004c0007 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | ATGCC others(1519): Show |
chr2 | 58041806 | 58164871 | ||
| a0005c0006 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | ATGCC others(1519): Show |
chr2 | 58041806 | 58164871 | ||
| a0006c0010 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | ATGCC others(1519): Show |
chr2 | 58041806 | 58164871 | ||
| a0007c0009 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | ATGCC others(1519): Show |
chr2 | 58041806 | 58164871 | ||
| a0008c0008 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | ATGCC others(1519): Show |
chr2 | 58041806 | 58164871 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1773 | 144 | 55 | 21 | 51 | 6 | 11 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0001c0001t0002 | 1/0 | 1773 | 69 | 2 | 15 | 39 | 3 | 9 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0001c0001t0003 | 0/0 | 1773 | 7 | 1 | 3 | 0 | 2 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0001c0001t0006 | 0/0 | 1784 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1779): Show |
chr2 | 58041806 | 58164871 |
| a0001c0003t0001 | 0/0 | 1773 | 15 | 15 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0001c0003t0004 | 0/0 | 1773 | 3 | 3 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0001c0004t0001 | 0/0 | 1773 | 3 | 0 | 3 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0002c0002t0001 | 0/0 | 1773 | 5 | 2 | 1 | 0 | 0 | 2 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0002c0002t0002 | 0/1 | 1773 | 85 | 6 | 23 | 42 | 3 | 10 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0002c0002t0005 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0003c0005t0001 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0004c0007t0002 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0005c0006t0002 | 0/0 | 1773 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0006c0010t0001 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0007c0009t0001 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| a0008c0008t0002 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | CTCGT others(1768): Show |
chr2 | 58041806 | 58164871 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0003t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0004t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0004t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0001c0004t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0002c0002t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0003c0005t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0003c0005t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0004c0007t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0005c0006t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0006c0010t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0007c0009t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| a0008c0008t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | GBR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | FIN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0219 | EUR | FIN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0103 | EUR | FIN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0286 | EUR | FIN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | CHS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0080 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0254 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0051 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0039 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0328 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0042 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0037 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0041 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0112 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0329 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0062 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0102 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0185 | EUR | IBS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0243 | EUR | IBS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0068 | EUR | IBS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0242 | EUR | IBS | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0263 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0272 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0073 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0072 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0076 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0132 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02004 | hp2 | a0001 | c0004 | t0001 | g0131 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0207 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02132 | hp2 | a0004 | c0007 | t0002 | g0218 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | CDX | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | CDX | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | CDX | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | CDX | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02293 | hp1 | a0001 | c0004 | t0001 | g0130 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0077 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0267 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0257 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0033 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02647 | hp1 | a0001 | c0003 | t0004 | g0011 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0288 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02683 | hp2 | a0005 | c0006 | t0002 | g0166 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0273 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0246 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0028 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0092 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02886 | hp2 | a0006 | c0010 | t0001 | g0148 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02896 | hp2 | a0001 | c0003 | t0004 | g0014 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02897 | hp1 | a0001 | c0003 | t0004 | g0013 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0269 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02970 | hp1 | a0003 | c0005 | t0001 | g0116 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0060 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0256 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0282 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03579 | hp1 | a0007 | c0009 | t0001 | g0124 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0111 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | PJL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0065 | SAS | BEB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | BEB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0281 | SAS | BEB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0025 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0045 | SAS | BEB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | STU | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | CHB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0268 | AFR | YRI | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | YRI | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0330 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18998 | hp2 | a0008 | c0008 | t0002 | g0232 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0261 | AFR | LWK | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0258 | AFR | LWK | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0271 | AFR | LWK | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0149 | AFR | LWK | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19076 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19084 | hp1 | a0002 | c0002 | t0005 | g0109 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | YRI | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0270 | AFR | YRI | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ASW | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ASW | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0038 | EUR | TSI | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0075 | SAS | GIH | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | GIH | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02109 | hp2 | a0003 | c0005 | t0001 | g0117 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | MSL | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | USA | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | USA | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | USA | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | USA | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | LWK | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | LWK | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0090 | REF | REF | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0188 | REF | REF | VRK2_chr2_58041806_58164871 | VRK2 | chr2 | 58041806 | 58164871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:58046866 | C | T | 1 | a0001 | 7 | HG01256.hp1 HG01258.hp1 HG01516.hp1 others(4): Show |
splice_region_variant | LOW | c.-8C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/13 | chr2 | 58046866 | |||||||
| chr2:58048935 | T | C | 1 | a0005 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.104T>C | p.Ile35Thr | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/13 | 172/1773 | 104/1527 | 35/508 | chr2 | 58048935 | |||
| chr2:58084100 | A | G | 1 | a0006 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.148A>G | p.Asn50Asp | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/13 | 216/1773 | 148/1527 | 50/508 | chr2 | 58084100 | |||
| chr2:58088400 | A | C | 1 | a0007 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.404A>C | p.Asn135Thr | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/13 | 472/1773 | 404/1527 | 135/508 | chr2 | 58088400 | |||
| chr2:58089679 | A | G | 2 | a0002 a0008 |
91 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(88): Show |
missense_variant | MODERATE | c.499A>G | p.Ile167Val | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/13 | 567/1773 | 499/1527 | 167/508 | chr2 | 58089679 | |||
| chr2:58139770 | G | C | 1 | a0008 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.961G>C | p.Gly321Arg | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/13 | 1029/1773 | 961/1527 | 321/508 | chr2 | 58139770 | |||
| chr2:58146446 | T | C | 1 | a0004 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.1154T>C | p.Ile385Thr | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/13 | 1222/1773 | 1154/1527 | 385/508 | chr2 | 58146446 | |||
| chr2:58159653 | T | G | 1 | a0003 | 2 | HG02109.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.1487T>G | p.Val496Gly | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 1555/1773 | 1487/1527 | 496/508 | chr2 | 58159653 | |||
| chr2:58159670 | T | C | 1 | a0003 | 2 | HG02109.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.1504T>C | p.Phe502Leu | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 1572/1773 | 1504/1527 | 502/508 | chr2 | 58159670 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:58123205 | T | C | 1 | a0001c0003 | 18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
synonymous_variant | LOW | c.648T>C | p.Phe216Phe | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/13 | 716/1773 | 648/1527 | 216/508 | chr2 | 58123205 | |||
| chr2:58159432 | T | C | 1 | a0001c0004 | 3 | HG01993.hp2 HG02004.hp2 HG02293.hp1 |
synonymous_variant | LOW | c.1266T>C | p.Tyr422Tyr | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 1334/1773 | 1266/1527 | 422/508 | chr2 | 58159432 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:58159750 | T | C | 1 | a0001c0003t0004 | 3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*57T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 57 | chr2 | 58159750 | ||||||
| chr2:58159797 | T | C | 1 | a0002c0002t0005 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*104T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 104 | chr2 | 58159797 | ||||||
| chr2:58159808 | A | AAGAGAAC others(4): Show |
1 | a0001c0001t0006 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*116_*126dupAGAGAA others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 127 | INFO_REALIGN_3_PRIME | chr2 | 58159808 | |||||
| chr2:58159865 | C | T | 8 | a0001c0001t0001 a0001c0003t0001 a0001c0003t0004 others(5): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*172C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 13/13 | 172 | chr2 | 58159865 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:58046916 | T | G | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6+48T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58046916 | |||||||
| chr2:58046924 | C | G | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6+56C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58046924 | |||||||
| chr2:58047105 | C | T | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-6+237C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047105 | |||||||
| chr2:58047191 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-6+323G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047191 | |||||||
| chr2:58047219 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-6+351G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047219 | |||||||
| chr2:58047361 | T | C | 1 | a0001c0001t0002g0018 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-6+493T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047361 | |||||||
| chr2:58047496 | C | T | 1 | a0001c0003t0001g0015 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-6+628C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047496 | |||||||
| chr2:58047531 | G | T | 1 | a0002c0002t0002g0329 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-6+663G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047531 | |||||||
| chr2:58047621 | G | A | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6+753G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047621 | |||||||
| chr2:58047634 | G | T | 1 | a0002c0002t0002g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-6+766G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58047634 | |||||||
| chr2:58047749 | C | CAGG | 82 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0259 others(79): Show |
84 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-6+886_-6+888dupGG others(1): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 58047749 | ||||||
| chr2:58048047 | A | T | 1 | a0001c0001t0001g0255 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5-780A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048047 | |||||||
| chr2:58048168 | A | C | 1 | a0001c0001t0001g0327 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-5-659A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048168 | |||||||
| chr2:58048210 | T | G | 3 | a0001c0003t0001g0256 a0001c0003t0001g0257 a0001c0003t0001g0258 |
3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-5-617T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048210 | |||||||
| chr2:58048367 | C | T | 2 | a0002c0002t0001g0253 a0002c0002t0002g0254 |
2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-5-460C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048367 | |||||||
| chr2:58048387 | A | G | 11 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(8): Show |
11 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-440A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048387 | |||||||
| chr2:58048531 | G | A | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(232): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-5-296G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048531 | |||||||
| chr2:58048555 | T | C | 2 | a0001c0001t0001g0259 a0001c0001t0001g0327 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-5-272T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048555 | |||||||
| chr2:58048563 | C | T | 2 | a0001c0003t0004g0013 a0001c0003t0004g0014 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5-264C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048563 | |||||||
| chr2:58048648 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-5-179A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048648 | |||||||
| chr2:58048775 | T | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-5-52T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 1/12 | chr2 | 58048775 | |||||||
| chr2:58048980 | C | G | 7 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(4): Show |
7 | HG01167.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.136+13C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58048980 | |||||||
| chr2:58049029 | A | G | 21 | a0001c0001t0001g0017 a0001c0001t0001g0259 a0001c0001t0001g0309 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.136+62A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58049029 | |||||||
| chr2:58049074 | A | G | 7 | a0002c0002t0002g0151 a0002c0002t0002g0152 a0002c0002t0002g0153 others(4): Show |
7 | HG00621.hp2 NA18961.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+107A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58049074 | |||||||
| chr2:58049145 | C | A | 104 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0027 others(101): Show |
105 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.136+178C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58049145 | |||||||
| chr2:58049884 | T | TTGAA | 4 | a0001c0001t0001g0147 a0002c0002t0001g0149 a0002c0002t0001g0150 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+934_136+937dup others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58049884 | ||||||
| chr2:58049896 | A | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0274 a0001c0001t0001g0275 others(37): Show |
42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.136+929A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58049896 | |||||||
| chr2:58050049 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0327 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.136+1082A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050049 | |||||||
| chr2:58050130 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.136+1163A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050130 | |||||||
| chr2:58050139 | G | T | 1 | a0001c0001t0001g0307 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.136+1172G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050139 | |||||||
| chr2:58050291 | T | C | 1 | a0001c0001t0001g0307 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.136+1324T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050291 | |||||||
| chr2:58050448 | C | T | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.136+1481C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050448 | |||||||
| chr2:58050456 | C | G | 24 | a0001c0001t0001g0017 a0001c0001t0001g0259 a0001c0001t0001g0309 others(21): Show |
24 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.136+1489C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050456 | |||||||
| chr2:58050555 | A | G | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+1588A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050555 | |||||||
| chr2:58050558 | A | G | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.136+1591A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050558 | |||||||
| chr2:58050708 | G | A | 12 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(9): Show |
12 | HG01167.hp1 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.136+1741G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050708 | |||||||
| chr2:58050762 | T | C | 2 | a0002c0002t0002g0021 a0002c0002t0002g0022 |
2 | HG01074.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.136+1795T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050762 | |||||||
| chr2:58050777 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.136+1810A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050777 | |||||||
| chr2:58050788 | C | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136+1821C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050788 | |||||||
| chr2:58050809 | A | G | 1 | a0001c0001t0002g0251 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.136+1842A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050809 | |||||||
| chr2:58050861 | T | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0274 a0001c0001t0001g0275 others(34): Show |
39 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.136+1894T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050861 | |||||||
| chr2:58050913 | C | T | 4 | a0001c0001t0001g0147 a0002c0002t0001g0149 a0002c0002t0001g0150 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+1946C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050913 | |||||||
| chr2:58050935 | C | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0274 a0001c0001t0001g0275 others(34): Show |
39 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.136+1968C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050935 | |||||||
| chr2:58050975 | T | A | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136+2008T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58050975 | |||||||
| chr2:58051033 | C | T | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+2066C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051033 | |||||||
| chr2:58051160 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136+2193A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051160 | |||||||
| chr2:58051197 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.136+2230T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051197 | |||||||
| chr2:58051336 | G | A | 2 | a0001c0003t0001g0009 a0001c0003t0001g0010 |
2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.136+2369G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051336 | |||||||
| chr2:58051475 | A | G | 24 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.136+2508A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051475 | |||||||
| chr2:58051489 | C | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136+2522C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051489 | |||||||
| chr2:58051546 | A | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0274 a0001c0001t0001g0275 others(37): Show |
42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.136+2579A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051546 | |||||||
| chr2:58051742 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.136+2775G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051742 | |||||||
| chr2:58051782 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.136+2815G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051782 | |||||||
| chr2:58051959 | A | T | 1 | a0001c0001t0001g0306 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.136+2992A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58051959 | |||||||
| chr2:58052015 | G | T | 6 | a0001c0003t0001g0267 a0001c0003t0001g0268 a0001c0003t0001g0269 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+3048G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052015 | |||||||
| chr2:58052151 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136+3184C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052151 | |||||||
| chr2:58052209 | A | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0274 a0001c0001t0001g0275 others(44): Show |
49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.136+3242A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052209 | |||||||
| chr2:58052313 | A | G | 7 | a0001c0001t0003g0241 a0001c0001t0003g0242 a0001c0001t0003g0243 others(4): Show |
7 | HG01256.hp1 HG01258.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+3346A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052313 | |||||||
| chr2:58052446 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0274 a0001c0001t0001g0275 others(41): Show |
46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.136+3479C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052446 | |||||||
| chr2:58052481 | G | A | 1 | a0001c0003t0001g0256 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.136+3514G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052481 | |||||||
| chr2:58052600 | C | CA | 26 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(23): Show |
27 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.136+3652dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58052600 | ||||||
| chr2:58052600 | CA | C | 14 | a0001c0001t0001g0146 a0001c0001t0001g0236 a0001c0001t0001g0264 others(11): Show |
14 | HG01243.hp2 HG01975.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.136+3652delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58052600 | ||||||
| chr2:58052920 | C | A | 1 | a0002c0002t0002g0024 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.136+3953C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58052920 | |||||||
| chr2:58053032 | C | G | 1 | a0001c0001t0001g0304 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.136+4065C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053032 | |||||||
| chr2:58053149 | C | A | 1 | a0001c0003t0001g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136+4182C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053149 | |||||||
| chr2:58053317 | A | G | 4 | a0001c0001t0001g0147 a0002c0002t0001g0149 a0002c0002t0001g0150 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+4350A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053317 | |||||||
| chr2:58053663 | A | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0125 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.136+4696A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053663 | |||||||
| chr2:58053708 | A | G | 1 | a0002c0002t0002g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.136+4741A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053708 | |||||||
| chr2:58053831 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136+4864A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053831 | |||||||
| chr2:58053912 | T | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0274 a0001c0001t0001g0275 others(34): Show |
39 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.136+4945T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053912 | |||||||
| chr2:58053930 | C | A | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+4963C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053930 | |||||||
| chr2:58053949 | T | C | 1 | a0001c0003t0001g0267 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.136+4982T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58053949 | |||||||
| chr2:58054007 | G | A | 1 | a0002c0002t0002g0273 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.136+5040G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58054007 | |||||||
| chr2:58054390 | G | GT | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0125 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.136+5435dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58054390 | ||||||
| chr2:58054431 | T | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136+5464T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58054431 | |||||||
| chr2:58054630 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.136+5663A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58054630 | |||||||
| chr2:58054777 | A | G | 22 | a0001c0001t0001g0017 a0001c0001t0001g0259 a0001c0001t0001g0311 others(19): Show |
22 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.136+5810A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58054777 | |||||||
| chr2:58055270 | G | A | 6 | a0001c0003t0001g0267 a0001c0003t0001g0268 a0001c0003t0001g0269 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+6303G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58055270 | |||||||
| chr2:58055384 | C | G | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+6417C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58055384 | |||||||
| chr2:58055799 | A | G | 2 | a0001c0003t0001g0012 a0001c0003t0001g0015 |
2 | HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.136+6832A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58055799 | |||||||
| chr2:58055985 | T | C | 1 | a0001c0001t0002g0167 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.136+7018T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58055985 | |||||||
| chr2:58056032 | GAA | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0274 a0001c0001t0001g0275 others(35): Show |
40 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.136+7066_136+7067d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056032 | |||||||
| chr2:58056035 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0274 a0001c0001t0001g0275 others(35): Show |
40 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.136+7068C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056035 | |||||||
| chr2:58056096 | C | G | 4 | a0001c0001t0001g0262 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | HG01243.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+7129C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056096 | |||||||
| chr2:58056112 | C | T | 2 | a0001c0001t0002g0233 a0001c0001t0002g0234 |
2 | NA18991.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.136+7145C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056112 | |||||||
| chr2:58056401 | G | A | 3 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.136+7434G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056401 | |||||||
| chr2:58056465 | T | C | 1 | a0001c0001t0002g0168 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.136+7498T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056465 | |||||||
| chr2:58056470 | C | G | 1 | a0001c0001t0001g0141 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.136+7503C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056470 | |||||||
| chr2:58056563 | G | A | 1 | a0002c0002t0001g0025 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.136+7596G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056563 | |||||||
| chr2:58056600 | C | G | 1 | a0001c0001t0001g0255 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.136+7633C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056600 | |||||||
| chr2:58056611 | A | ACT | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(245): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.136+7646_136+7647d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58056611 | ||||||
| chr2:58056619 | C | A | 2 | a0001c0003t0001g0261 a0001c0003t0001g0263 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.136+7652C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056619 | |||||||
| chr2:58056744 | G | A | 2 | a0002c0002t0002g0028 a0002c0002t0002g0029 |
2 | HG02738.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.136+7777G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056744 | |||||||
| chr2:58056745 | C | T | 1 | a0002c0002t0002g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.136+7778C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056745 | |||||||
| chr2:58056948 | A | G | 1 | a0001c0001t0002g0219 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.136+7981A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056948 | |||||||
| chr2:58056976 | C | T | 1 | a0001c0001t0002g0005 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.136+8009C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58056976 | |||||||
| chr2:58057035 | G | A | 1 | a0001c0003t0001g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136+8068G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057035 | |||||||
| chr2:58057063 | T | C | 1 | a0002c0002t0002g0030 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.136+8096T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057063 | |||||||
| chr2:58057081 | C | T | 21 | a0001c0001t0001g0017 a0001c0001t0001g0259 a0001c0001t0001g0309 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.136+8114C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057081 | |||||||
| chr2:58057113 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0327 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.136+8146G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057113 | |||||||
| chr2:58057411 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.136+8444T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057411 | |||||||
| chr2:58057414 | T | C | 3 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0002g0286 |
3 | HG00323.hp2 HG00597.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.136+8447T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057414 | |||||||
| chr2:58057503 | CTCTT | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(131): Show |
138 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.136+8540_136+8543d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58057503 | ||||||
| chr2:58057505 | CTT | C | 6 | a0001c0001t0001g0105 a0001c0001t0002g0197 a0002c0002t0002g0107 others(3): Show |
6 | HG00408.hp1 HG00423.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+8540_136+8541d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58057505 | ||||||
| chr2:58057533 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136+8566G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057533 | |||||||
| chr2:58057539 | A | T | 1 | a0002c0002t0002g0103 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.136+8572A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057539 | |||||||
| chr2:58057616 | T | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0274 a0001c0001t0001g0275 others(34): Show |
39 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.136+8649T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057616 | |||||||
| chr2:58057765 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136+8798A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057765 | |||||||
| chr2:58057873 | C | A | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.136+8906C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58057873 | |||||||
| chr2:58058400 | A | G | 1 | a0005c0006t0002g0166 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.136+9433A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58058400 | |||||||
| chr2:58058520 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136+9553G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58058520 | |||||||
| chr2:58058599 | T | C | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.136+9632T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58058599 | |||||||
| chr2:58058653 | G | A | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+9686G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58058653 | |||||||
| chr2:58058732 | C | G | 1 | a0002c0002t0002g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.136+9765C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58058732 | |||||||
| chr2:58059192 | A | G | 2 | a0001c0003t0001g0261 a0001c0003t0001g0263 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.136+10225A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059192 | |||||||
| chr2:58059258 | A | G | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.136+10291A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059258 | |||||||
| chr2:58059313 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.136+10346G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059313 | |||||||
| chr2:58059315 | C | G | 21 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.136+10348C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059315 | |||||||
| chr2:58059566 | C | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136+10599C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059566 | |||||||
| chr2:58059709 | G | A | 1 | a0001c0003t0001g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.136+10742G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059709 | |||||||
| chr2:58059778 | ATAGT | A | 4 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
4 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+10814_136+1081 others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58059778 | ||||||
| chr2:58059836 | A | G | 1 | a0002c0002t0002g0100 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.136+10869A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58059836 | |||||||
| chr2:58060132 | C | A | 1 | a0001c0001t0002g0173 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.136+11165C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060132 | |||||||
| chr2:58060221 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.136+11254G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060221 | |||||||
| chr2:58060339 | A | G | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.136+11372A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060339 | |||||||
| chr2:58060364 | G | T | 2 | a0002c0002t0001g0149 a0002c0002t0001g0150 |
2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.136+11397G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060364 | |||||||
| chr2:58060373 | T | G | 7 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(4): Show |
7 | HG01109.hp2 HG02145.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.136+11406T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060373 | |||||||
| chr2:58060495 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.136+11528A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060495 | |||||||
| chr2:58060543 | T | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0125 a0001c0001t0001g0126 |
5 | NA18943.hp2 NA18947.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+11576T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060543 | |||||||
| chr2:58060605 | G | A | 1 | a0002c0002t0002g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.136+11638G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060605 | |||||||
| chr2:58060822 | C | T | 19 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(16): Show |
19 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.136+11855C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060822 | |||||||
| chr2:58060887 | A | G | 1 | a0002c0002t0002g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.136+11920A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58060887 | |||||||
| chr2:58061021 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.136+12054A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061021 | |||||||
| chr2:58061317 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.136+12350A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061317 | |||||||
| chr2:58061418 | G | A | 1 | a0001c0001t0003g0241 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.136+12451G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061418 | |||||||
| chr2:58061428 | A | G | 4 | a0001c0001t0001g0147 a0002c0002t0001g0149 a0002c0002t0001g0150 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+12461A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061428 | |||||||
| chr2:58061441 | A | T | 3 | a0001c0003t0001g0256 a0001c0003t0001g0257 a0001c0003t0001g0258 |
3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.136+12474A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061441 | |||||||
| chr2:58061550 | C | T | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.136+12583C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061550 | |||||||
| chr2:58061553 | A | G | 1 | a0002c0002t0002g0099 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.136+12586A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061553 | |||||||
| chr2:58061952 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.136+12985A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58061952 | |||||||
| chr2:58062191 | A | G | 1 | a0001c0001t0001g0283 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.136+13224A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062191 | |||||||
| chr2:58062262 | G | C | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+13295G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062262 | |||||||
| chr2:58062506 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.136+13539C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062506 | |||||||
| chr2:58062673 | A | C | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.136+13706A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062673 | |||||||
| chr2:58062855 | G | A | 11 | a0001c0001t0002g0016 a0001c0003t0001g0261 a0001c0003t0001g0263 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.136+13888G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062855 | |||||||
| chr2:58062862 | A | G | 2 | a0001c0003t0001g0256 a0001c0003t0001g0258 |
2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.136+13895A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062862 | |||||||
| chr2:58062910 | C | A | 1 | a0001c0001t0002g0174 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.136+13943C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062910 | |||||||
| chr2:58062916 | T | C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0125 others(17): Show |
23 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.136+13949T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062916 | |||||||
| chr2:58062981 | G | A | 4 | a0001c0001t0001g0147 a0002c0002t0001g0149 a0002c0002t0001g0150 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+14014G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58062981 | |||||||
| chr2:58063039 | C | T | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.136+14072C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063039 | |||||||
| chr2:58063086 | A | G | 1 | a0008c0008t0002g0232 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.136+14119A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063086 | |||||||
| chr2:58063132 | G | C | 1 | a0001c0001t0002g0174 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.136+14165G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063132 | |||||||
| chr2:58063241 | G | GT | 14 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(11): Show |
14 | HG00738.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.136+14290dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58063241 | ||||||
| chr2:58063241 | GT | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0019 others(43): Show |
49 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.136+14290delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58063241 | ||||||
| chr2:58063248 | T | G | 21 | a0001c0001t0001g0017 a0001c0001t0001g0259 a0001c0001t0001g0309 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.136+14281T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063248 | |||||||
| chr2:58063267 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.136+14300G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063267 | |||||||
| chr2:58063306 | G | C | 21 | a0001c0001t0001g0017 a0001c0001t0001g0259 a0001c0001t0001g0309 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.136+14339G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063306 | |||||||
| chr2:58063413 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.136+14446T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063413 | |||||||
| chr2:58063421 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136+14454G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063421 | |||||||
| chr2:58063474 | A | C | 4 | a0001c0001t0001g0147 a0002c0002t0001g0149 a0002c0002t0001g0150 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+14507A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063474 | |||||||
| chr2:58063479 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.136+14512A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063479 | |||||||
| chr2:58063506 | A | G | 7 | a0002c0002t0002g0151 a0002c0002t0002g0152 a0002c0002t0002g0153 others(4): Show |
7 | HG00621.hp2 NA18961.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+14539A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063506 | |||||||
| chr2:58063514 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.136+14547T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063514 | |||||||
| chr2:58063569 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.136+14602A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063569 | |||||||
| chr2:58063679 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.136+14712T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063679 | |||||||
| chr2:58063774 | A | G | 19 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(16): Show |
19 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.136+14807A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58063774 | |||||||
| chr2:58064397 | A | G | 1 | a0001c0003t0001g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.136+15430A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58064397 | |||||||
| chr2:58064493 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.136+15526G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58064493 | |||||||
| chr2:58064524 | G | C | 1 | a0002c0002t0002g0033 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.136+15557G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58064524 | |||||||
| chr2:58064544 | C | T | 21 | a0001c0001t0001g0017 a0001c0001t0001g0259 a0001c0001t0001g0309 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.136+15577C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58064544 | |||||||
| chr2:58064875 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.136+15908A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58064875 | |||||||
| chr2:58065294 | CT | C | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+16328delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065294 | |||||||
| chr2:58065589 | C | T | 4 | a0001c0001t0001g0262 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | HG01243.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+16622C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065589 | |||||||
| chr2:58065705 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.136+16738T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065705 | |||||||
| chr2:58065728 | A | T | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.136+16761A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065728 | |||||||
| chr2:58065732 | A | G | 1 | a0002c0002t0002g0273 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.136+16765A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065732 | |||||||
| chr2:58065827 | G | A | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+16860G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065827 | |||||||
| chr2:58065896 | T | G | 6 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+16929T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58065896 | |||||||
| chr2:58066051 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.136+17084A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58066051 | |||||||
| chr2:58066165 | C | G | 4 | a0001c0001t0001g0147 a0002c0002t0001g0149 a0002c0002t0001g0150 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+17198C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58066165 | |||||||
| chr2:58066592 | G | C | 1 | a0002c0002t0002g0033 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.137-17497G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58066592 | |||||||
| chr2:58066792 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-17297G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58066792 | |||||||
| chr2:58066988 | G | A | 9 | a0001c0001t0002g0016 a0001c0003t0001g0261 a0001c0003t0001g0263 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.137-17101G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58066988 | |||||||
| chr2:58067321 | T | C | 1 | a0002c0002t0001g0149 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.137-16768T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067321 | |||||||
| chr2:58067401 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.137-16688C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067401 | |||||||
| chr2:58067549 | T | G | 4 | a0001c0001t0001g0262 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | HG01243.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-16540T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067549 | |||||||
| chr2:58067782 | A | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0125 others(17): Show |
23 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.137-16307A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067782 | |||||||
| chr2:58067844 | A | G | 1 | a0002c0002t0002g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.137-16245A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067844 | |||||||
| chr2:58067888 | C | A | 1 | a0001c0001t0002g0177 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.137-16201C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067888 | |||||||
| chr2:58067938 | G | GT | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0125 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.137-16142dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58067938 | ||||||
| chr2:58067982 | T | G | 1 | a0002c0002t0002g0288 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.137-16107T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067982 | |||||||
| chr2:58067989 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-16100G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58067989 | |||||||
| chr2:58068193 | G | A | 2 | a0001c0001t0003g0242 a0001c0001t0003g0243 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.137-15896G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068193 | |||||||
| chr2:58068437 | C | G | 2 | a0001c0001t0001g0123 a0007c0009t0001g0124 |
2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.137-15652C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068437 | |||||||
| chr2:58068487 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-15602A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068487 | |||||||
| chr2:58068630 | T | A | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-15459T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068630 | |||||||
| chr2:58068811 | GA | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0101 others(57): Show |
62 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.137-15260delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58068811 | ||||||
| chr2:58068811 | GAA | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0019 others(180): Show |
187 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.137-15261_137-1526 others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58068811 | ||||||
| chr2:58068824 | A | C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(33): Show |
39 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.137-15265A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068824 | |||||||
| chr2:58068830 | C | A | 1 | a0001c0001t0002g0185 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.137-15259C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068830 | |||||||
| chr2:58068839 | G | A | 2 | a0001c0003t0001g0261 a0001c0003t0001g0263 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.137-15250G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068839 | |||||||
| chr2:58068844 | T | C | 1 | a0002c0002t0002g0046 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.137-15245T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068844 | |||||||
| chr2:58068949 | A | G | 1 | a0001c0003t0001g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.137-15140A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58068949 | |||||||
| chr2:58069191 | A | C | 19 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(16): Show |
19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.137-14898A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069191 | |||||||
| chr2:58069193 | T | A | 1 | a0002c0002t0002g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.137-14896T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069193 | |||||||
| chr2:58069362 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0019 others(56): Show |
62 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.137-14727C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069362 | |||||||
| chr2:58069458 | T | C | 2 | a0001c0003t0001g0268 a0001c0003t0001g0269 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.137-14631T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069458 | |||||||
| chr2:58069643 | T | A | 1 | a0001c0003t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.137-14446T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069643 | |||||||
| chr2:58069667 | T | G | 1 | a0002c0002t0001g0149 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.137-14422T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069667 | |||||||
| chr2:58069755 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(245): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.137-14334A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58069755 | |||||||
| chr2:58070093 | C | T | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-13996C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070093 | |||||||
| chr2:58070180 | C | G | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.137-13909C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070180 | |||||||
| chr2:58070211 | T | A | 1 | a0002c0002t0002g0095 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.137-13878T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070211 | |||||||
| chr2:58070283 | C | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.137-13806C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070283 | |||||||
| chr2:58070344 | C | T | 1 | a0001c0001t0002g0008 | 2 | HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.137-13745C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070344 | |||||||
| chr2:58070378 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.137-13711G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070378 | |||||||
| chr2:58070529 | G | A | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.137-13560G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070529 | |||||||
| chr2:58070618 | T | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | NA18955.hp2 NA18992.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.137-13471T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070618 | |||||||
| chr2:58070774 | T | G | 3 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0002g0286 |
3 | HG00323.hp2 HG00597.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.137-13315T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58070774 | |||||||
| chr2:58071192 | A | G | 1 | a0002c0002t0001g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137-12897A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071192 | |||||||
| chr2:58071425 | G | A | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.137-12664G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071425 | |||||||
| chr2:58071433 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.137-12656A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071433 | |||||||
| chr2:58071594 | C | G | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.137-12495C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071594 | |||||||
| chr2:58071673 | C | G | 1 | a0002c0002t0001g0149 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.137-12416C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071673 | |||||||
| chr2:58071753 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0179 |
2 | HG00738.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.137-12336G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071753 | |||||||
| chr2:58071856 | A | G | 20 | a0001c0001t0001g0017 a0001c0001t0001g0259 a0001c0001t0001g0309 others(17): Show |
20 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.137-12233A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071856 | |||||||
| chr2:58071944 | A | G | 1 | a0001c0001t0002g0168 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.137-12145A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58071944 | |||||||
| chr2:58072069 | G | T | 4 | a0002c0002t0002g0036 a0002c0002t0002g0037 a0002c0002t0002g0038 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-12020G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072069 | |||||||
| chr2:58072095 | A | G | 1 | a0004c0007t0002g0218 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.137-11994A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072095 | |||||||
| chr2:58072191 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.137-11898A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072191 | |||||||
| chr2:58072225 | G | A | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.137-11864G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072225 | |||||||
| chr2:58072328 | A | G | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-11761A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072328 | |||||||
| chr2:58072489 | G | T | 1 | a0001c0001t0001g0306 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.137-11600G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072489 | |||||||
| chr2:58072608 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.137-11481C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072608 | |||||||
| chr2:58072622 | G | T | 1 | a0001c0001t0001g0301 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.137-11467G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072622 | |||||||
| chr2:58072760 | A | G | 1 | a0002c0002t0002g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.137-11329A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072760 | |||||||
| chr2:58072958 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0019 others(58): Show |
64 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.137-11131C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58072958 | |||||||
| chr2:58073295 | G | C | 1 | a0001c0001t0001g0031 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.137-10794G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58073295 | |||||||
| chr2:58073349 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-10740C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58073349 | |||||||
| chr2:58073636 | T | TTA | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-10437_137-1043 others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58073636 | ||||||
| chr2:58073648 | A | ATATATT | 7 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0183 others(4): Show |
7 | HG01433.hp2 HG04199.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.137-10411_137-1040 others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58073648 | ||||||
| chr2:58073648 | ATATATT | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(223): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.137-10411_137-1040 others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58073648 | ||||||
| chr2:58073648 | ATATATTT others(5): Show |
A | 1 | a0002c0002t0002g0035 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.137-10417_137-1040 others(16): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58073648 | ||||||
| chr2:58073648 | ATATATTT others(11): Show |
A | 2 | a0001c0003t0001g0268 a0001c0003t0001g0269 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.137-10423_137-1040 others(22): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58073648 | ||||||
| chr2:58073779 | C | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(59): Show |
64 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.137-10310C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58073779 | |||||||
| chr2:58073880 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(17): Show |
22 | HG01928.hp2 HG01934.hp2 HG02886.hp1 others(19): Show |
intron_variant | MODIFIER | c.137-10209A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58073880 | |||||||
| chr2:58074025 | T | C | 1 | a0004c0007t0002g0218 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.137-10064T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074025 | |||||||
| chr2:58074202 | T | G | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-9887T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074202 | |||||||
| chr2:58074239 | C | G | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG01243.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.137-9850C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074239 | |||||||
| chr2:58074372 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0019 others(56): Show |
62 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.137-9717A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074372 | |||||||
| chr2:58074413 | G | C | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137-9676G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074413 | |||||||
| chr2:58074460 | G | C | 4 | a0001c0001t0001g0147 a0002c0002t0001g0149 a0002c0002t0001g0150 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-9629G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074460 | |||||||
| chr2:58074503 | C | T | 3 | a0001c0001t0001g0300 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | HG01975.hp1 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.137-9586C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074503 | |||||||
| chr2:58074715 | C | T | 5 | a0002c0002t0002g0084 a0002c0002t0002g0085 a0002c0002t0002g0099 others(2): Show |
5 | NA18943.hp1 NA18951.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-9374C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074715 | |||||||
| chr2:58074790 | A | T | 1 | a0001c0001t0002g0286 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.137-9299A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074790 | |||||||
| chr2:58074825 | G | T | 1 | a0002c0002t0002g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.137-9264G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074825 | |||||||
| chr2:58074848 | C | A | 1 | a0001c0003t0001g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.137-9241C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074848 | |||||||
| chr2:58074974 | T | C | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG02523.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.137-9115T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58074974 | |||||||
| chr2:58075050 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-9039A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075050 | |||||||
| chr2:58075182 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.137-8907A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075182 | |||||||
| chr2:58075219 | C | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0125 others(17): Show |
23 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.137-8870C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075219 | |||||||
| chr2:58075258 | T | A | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137-8831T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075258 | |||||||
| chr2:58075374 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-8715G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075374 | |||||||
| chr2:58075446 | C | A | 1 | a0002c0002t0002g0051 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.137-8643C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075446 | |||||||
| chr2:58075478 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-8611G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075478 | |||||||
| chr2:58075727 | G | A | 25 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(22): Show |
25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.137-8362G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075727 | |||||||
| chr2:58075863 | A | ACTT | 25 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(22): Show |
25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.137-8226_137-8225i others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075863 | |||||||
| chr2:58075865 | A | T | 25 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(22): Show |
25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.137-8224A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075865 | |||||||
| chr2:58075866 | A | AGAGTACT others(25): Show |
25 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(22): Show |
25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.137-8223_137-8222i others(34): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075866 | |||||||
| chr2:58075956 | G | C | 22 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(19): Show |
22 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.137-8133G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58075956 | |||||||
| chr2:58076106 | C | CT | 7 | a0001c0001t0002g0172 a0001c0001t0002g0214 a0001c0001t0002g0215 others(4): Show |
7 | HG00735.hp2 HG01358.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-7965dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58076106 | ||||||
| chr2:58076106 | CT | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
133 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(130): Show |
intron_variant | MODIFIER | c.137-7965delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58076106 | ||||||
| chr2:58076309 | C | A | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG01167.hp1 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-7780C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076309 | |||||||
| chr2:58076378 | A | G | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.137-7711A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076378 | |||||||
| chr2:58076487 | A | C | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.137-7602A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076487 | |||||||
| chr2:58076494 | T | A | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137-7595T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076494 | |||||||
| chr2:58076606 | T | A | 1 | a0002c0002t0002g0288 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.137-7483T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076606 | |||||||
| chr2:58076607 | T | G | 1 | a0002c0002t0002g0288 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.137-7482T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076607 | |||||||
| chr2:58076608 | T | G | 1 | a0002c0002t0002g0288 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.137-7481T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076608 | |||||||
| chr2:58076699 | A | G | 1 | a0002c0002t0002g0082 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.137-7390A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076699 | |||||||
| chr2:58076758 | C | T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(43): Show |
48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.137-7331C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076758 | |||||||
| chr2:58076762 | C | A | 7 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(4): Show |
7 | HG01993.hp2 HG02004.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-7327C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076762 | |||||||
| chr2:58076877 | A | T | 13 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(10): Show |
13 | HG01167.hp1 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.137-7212A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076877 | |||||||
| chr2:58076916 | C | T | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-7173C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076916 | |||||||
| chr2:58076963 | T | C | 1 | a0002c0002t0002g0288 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.137-7126T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58076963 | |||||||
| chr2:58077135 | A | G | 4 | a0001c0001t0001g0147 a0002c0002t0001g0149 a0002c0002t0001g0150 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-6954A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077135 | |||||||
| chr2:58077260 | A | G | 1 | a0002c0002t0002g0081 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.137-6829A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077260 | |||||||
| chr2:58077283 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.137-6806T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077283 | |||||||
| chr2:58077313 | C | T | 10 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0031 others(7): Show |
10 | HG01928.hp2 HG01934.hp2 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.137-6776C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077313 | |||||||
| chr2:58077519 | AT | A | 24 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(21): Show |
24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.137-6560delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58077519 | ||||||
| chr2:58077532 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.137-6557C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077532 | |||||||
| chr2:58077660 | T | G | 1 | a0002c0002t0002g0091 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.137-6429T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077660 | |||||||
| chr2:58077743 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.137-6346G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077743 | |||||||
| chr2:58077908 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137-6181A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58077908 | |||||||
| chr2:58078140 | T | C | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | NA18970.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.137-5949T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078140 | |||||||
| chr2:58078330 | A | G | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-5759A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078330 | |||||||
| chr2:58078389 | T | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137-5700T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078389 | |||||||
| chr2:58078610 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.137-5479A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078610 | |||||||
| chr2:58078616 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(43): Show |
48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.137-5473G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078616 | |||||||
| chr2:58078761 | A | G | 1 | a0002c0002t0002g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.137-5328A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078761 | |||||||
| chr2:58078801 | G | A | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-5288G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078801 | |||||||
| chr2:58078846 | T | C | 4 | a0001c0001t0002g0172 a0001c0001t0002g0214 a0001c0001t0002g0215 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-5243T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078846 | |||||||
| chr2:58078876 | G | A | 9 | a0002c0002t0002g0051 a0002c0002t0002g0224 a0002c0002t0002g0226 others(6): Show |
9 | HG01069.hp1 HG02027.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.137-5213G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078876 | |||||||
| chr2:58078925 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.137-5164C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58078925 | |||||||
| chr2:58079593 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.137-4496A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58079593 | |||||||
| chr2:58079676 | G | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(42): Show |
47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.137-4413G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58079676 | |||||||
| chr2:58079902 | A | G | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(310): Show |
321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.137-4187A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58079902 | |||||||
| chr2:58080213 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.137-3876A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080213 | |||||||
| chr2:58080331 | G | T | 24 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(21): Show |
24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.137-3758G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080331 | |||||||
| chr2:58080458 | C | T | 5 | a0001c0001t0002g0173 a0001c0001t0002g0182 a0001c0001t0002g0212 others(2): Show |
5 | HG02027.hp2 HG02074.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-3631C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080458 | |||||||
| chr2:58080520 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.137-3569A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080520 | |||||||
| chr2:58080544 | A | G | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-3545A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080544 | |||||||
| chr2:58080648 | G | C | 1 | a0001c0001t0002g0191 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.137-3441G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080648 | |||||||
| chr2:58080834 | A | C | 6 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(3): Show |
6 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.137-3255A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080834 | |||||||
| chr2:58080868 | C | G | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-3221C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080868 | |||||||
| chr2:58080964 | G | T | 1 | a0001c0001t0002g0211 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.137-3125G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58080964 | |||||||
| chr2:58081024 | C | A | 21 | a0001c0001t0001g0017 a0001c0001t0001g0259 a0001c0001t0001g0309 others(18): Show |
21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.137-3065C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081024 | |||||||
| chr2:58081126 | G | T | 26 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(23): Show |
26 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.137-2963G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081126 | |||||||
| chr2:58081217 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.137-2872A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081217 | |||||||
| chr2:58081321 | C | A | 1 | a0001c0001t0001g0308 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.137-2768C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081321 | |||||||
| chr2:58081323 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0106 |
3 | HG00735.hp1 HG01261.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.137-2766G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081323 | |||||||
| chr2:58081365 | T | C | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.137-2724T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081365 | |||||||
| chr2:58081386 | A | G | 1 | a0002c0002t0001g0149 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.137-2703A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081386 | |||||||
| chr2:58081518 | T | C | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-2571T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081518 | |||||||
| chr2:58081561 | T | C | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-2528T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081561 | |||||||
| chr2:58081597 | T | A | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.137-2492T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081597 | |||||||
| chr2:58081857 | C | CGT | 95 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0027 others(92): Show |
97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.137-2191_137-2190d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | ||||||
| chr2:58081857 | C | CGTGT | 26 | a0001c0001t0001g0031 a0001c0001t0001g0093 a0001c0001t0001g0119 others(23): Show |
27 | HG00438.hp1 HG00741.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.137-2193_137-2190d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | ||||||
| chr2:58081857 | C | CGTGTGT | 5 | a0001c0001t0001g0002 a0001c0001t0001g0216 a0001c0001t0001g0236 others(2): Show |
7 | HG01515.hp1 NA18945.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-2195_137-2190d others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | ||||||
| chr2:58081857 | C | CGTGTGTG others(1): Show |
3 | a0001c0001t0001g0235 a0001c0003t0001g0268 a0001c0003t0001g0269 |
3 | HG02922.hp1 NA18906.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.137-2197_137-2190d others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | ||||||
| chr2:58081857 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.137-2199_137-2190d others(12): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | ||||||
| chr2:58081857 | CGT | C | 90 | a0001c0001t0001g0017 a0001c0001t0001g0096 a0001c0001t0001g0097 others(87): Show |
92 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.137-2191_137-2190d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | ||||||
| chr2:58081857 | CGTGT | C | 4 | a0001c0001t0001g0058 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG01167.hp1 HG02040.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-2193_137-2190d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | ||||||
| chr2:58081857 | CGTGTGT | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0019 others(22): Show |
28 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.137-2195_137-2190d others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | ||||||
| chr2:58081857 | CGTGTGTG others(1): Show |
C | 17 | a0001c0001t0001g0020 a0001c0001t0001g0114 a0001c0001t0001g0115 others(14): Show |
17 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.137-2197_137-2190d others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | ||||||
| chr2:58081857 | CGTGTGTG others(3): Show |
C | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-2199_137-2190d others(12): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 58081857 | ||||||
| chr2:58081931 | G | C | 1 | a0001c0001t0002g0233 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.137-2158G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58081931 | |||||||
| chr2:58082239 | T | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(61): Show |
67 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.137-1850T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082239 | |||||||
| chr2:58082288 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.137-1801G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082288 | |||||||
| chr2:58082395 | T | A | 1 | a0002c0002t0002g0064 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.137-1694T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082395 | |||||||
| chr2:58082472 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.137-1617G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082472 | |||||||
| chr2:58082595 | G | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(144): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.137-1494G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082595 | |||||||
| chr2:58082596 | A | G | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-1493A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082596 | |||||||
| chr2:58082617 | T | TAA | 15 | a0001c0001t0001g0017 a0001c0001t0001g0142 a0001c0001t0001g0143 others(12): Show |
15 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.137-1472_137-1471i others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082617 | |||||||
| chr2:58082732 | A | G | 1 | a0002c0002t0002g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.137-1357A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082732 | |||||||
| chr2:58082824 | T | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0133 others(8): Show |
12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.137-1265T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082824 | |||||||
| chr2:58082896 | T | G | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-1193T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082896 | |||||||
| chr2:58082927 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.137-1162T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082927 | |||||||
| chr2:58082981 | G | A | 1 | a0002c0002t0002g0024 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.137-1108G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58082981 | |||||||
| chr2:58083124 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137-965A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58083124 | |||||||
| chr2:58083144 | C | T | 24 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(21): Show |
24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.137-945C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58083144 | |||||||
| chr2:58083438 | A | G | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-651A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58083438 | |||||||
| chr2:58083559 | G | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(41): Show |
46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.137-530G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58083559 | |||||||
| chr2:58083659 | A | T | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-430A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58083659 | |||||||
| chr2:58083747 | T | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0179 |
2 | HG00738.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.137-342T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 2/12 | chr2 | 58083747 | |||||||
| chr2:58084152 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0327 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.186+14A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/12 | chr2 | 58084152 | |||||||
| chr2:58084489 | A | G | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.186+351A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/12 | chr2 | 58084489 | |||||||
| chr2:58084549 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.187-332T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/12 | chr2 | 58084549 | |||||||
| chr2:58084615 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.187-266G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/12 | chr2 | 58084615 | |||||||
| chr2:58084730 | T | G | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.187-151T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/12 | chr2 | 58084730 | |||||||
| chr2:58084858 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.187-23A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 3/12 | chr2 | 58084858 | |||||||
| chr2:58085150 | A | G | 2 | a0001c0001t0002g0209 a0001c0001t0002g0217 |
2 | HG02015.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.256+200A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085150 | |||||||
| chr2:58085237 | A | T | 1 | a0001c0003t0001g0015 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.256+287A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085237 | |||||||
| chr2:58085298 | A | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.256+348A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085298 | |||||||
| chr2:58085388 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.256+438A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085388 | |||||||
| chr2:58085676 | T | G | 1 | a0002c0002t0002g0033 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.257-663T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085676 | |||||||
| chr2:58085687 | A | G | 2 | a0002c0002t0002g0079 a0002c0002t0002g0080 |
2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.257-652A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085687 | |||||||
| chr2:58085930 | C | CT | 65 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(62): Show |
67 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.257-393dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 58085930 | ||||||
| chr2:58085930 | CT | C | 13 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(10): Show |
13 | HG00408.hp1 HG00558.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.257-393delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 58085930 | ||||||
| chr2:58085930 | CTTTTTTT others(1): Show |
C | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.257-400_257-393del others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 58085930 | ||||||
| chr2:58085982 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0101 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.257-357A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58085982 | |||||||
| chr2:58086052 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.257-287A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58086052 | |||||||
| chr2:58086196 | T | G | 1 | a0001c0001t0001g0053 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.257-143T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58086196 | |||||||
| chr2:58086211 | GA | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(44): Show |
49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.257-120delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 58086211 | ||||||
| chr2:58086217 | A | C | 1 | a0001c0001t0001g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.257-122A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58086217 | |||||||
| chr2:58086237 | C | T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0208 a0001c0001t0006g0207 |
3 | HG02083.hp1 NA19056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.257-102C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58086237 | |||||||
| chr2:58086239 | A | G | 1 | a0002c0002t0002g0153 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.257-100A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 4/12 | chr2 | 58086239 | |||||||
| chr2:58086467 | A | G | 3 | a0001c0003t0001g0256 a0001c0003t0001g0257 a0001c0003t0001g0258 |
3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.344+41A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58086467 | |||||||
| chr2:58086998 | T | G | 1 | a0002c0002t0002g0103 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.344+572T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58086998 | |||||||
| chr2:58087007 | A | G | 7 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(4): Show |
7 | HG01109.hp2 HG01243.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+581A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087007 | |||||||
| chr2:58087118 | G | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(88): Show |
93 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.344+692G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087118 | |||||||
| chr2:58087174 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.344+748T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087174 | |||||||
| chr2:58087487 | C | T | 3 | a0002c0002t0002g0060 a0002c0002t0002g0092 a0002c0002t0002g0102 |
3 | HG01496.hp1 HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.345-854C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087487 | |||||||
| chr2:58087501 | A | G | 4 | a0001c0001t0002g0172 a0001c0001t0002g0214 a0001c0001t0002g0215 others(1): Show |
4 | HG00735.hp2 HG01358.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-840A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087501 | |||||||
| chr2:58087502 | A | G | 5 | a0002c0002t0002g0227 a0002c0002t0002g0228 a0002c0002t0002g0229 others(2): Show |
5 | HG02027.hp1 HG02040.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-839A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087502 | |||||||
| chr2:58087677 | T | C | 1 | a0002c0002t0002g0030 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.345-664T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087677 | |||||||
| chr2:58087699 | A | G | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.345-642A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087699 | |||||||
| chr2:58087718 | G | C | 2 | a0002c0002t0002g0281 a0002c0002t0002g0282 |
2 | HG03490.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.345-623G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087718 | |||||||
| chr2:58087726 | T | C | 11 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-615T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087726 | |||||||
| chr2:58087972 | C | A | 1 | a0002c0002t0002g0226 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.345-369C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58087972 | |||||||
| chr2:58088123 | T | G | 25 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(22): Show |
25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.345-218T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 5/12 | chr2 | 58088123 | |||||||
| chr2:58088467 | A | T | 1 | a0001c0001t0002g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.450+21A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088467 | |||||||
| chr2:58088500 | T | C | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.450+54T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088500 | |||||||
| chr2:58088657 | G | C | 1 | a0002c0002t0002g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.450+211G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088657 | |||||||
| chr2:58088707 | A | G | 2 | a0002c0002t0002g0231 a0006c0010t0001g0148 |
2 | HG02027.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.450+261A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088707 | |||||||
| chr2:58088867 | T | A | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.450+421T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088867 | |||||||
| chr2:58088946 | A | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(19): Show |
25 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.450+500A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088946 | |||||||
| chr2:58088985 | A | C | 1 | a0001c0001t0002g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.450+539A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58088985 | |||||||
| chr2:58089052 | A | G | 25 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(22): Show |
25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.451-579A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58089052 | |||||||
| chr2:58089317 | CTA | C | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-312_451-311del others(2): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 58089317 | ||||||
| chr2:58089367 | A | G | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.451-264A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 6/12 | chr2 | 58089367 | |||||||
| chr2:58090073 | A | G | 19 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(16): Show |
19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.543+350A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090073 | |||||||
| chr2:58090270 | C | T | 1 | a0006c0010t0001g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.543+547C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090270 | |||||||
| chr2:58090400 | C | CA | 25 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0056 others(22): Show |
25 | HG00423.hp1 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.543+698dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58090400 | ||||||
| chr2:58090486 | A | G | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+763A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090486 | |||||||
| chr2:58090669 | G | A | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+946G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090669 | |||||||
| chr2:58090786 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.543+1063C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090786 | |||||||
| chr2:58090787 | G | A | 3 | a0001c0001t0002g0016 a0003c0005t0001g0116 a0003c0005t0001g0117 |
3 | HG02109.hp2 HG02970.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.543+1064G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090787 | |||||||
| chr2:58090896 | A | G | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+1173A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58090896 | |||||||
| chr2:58091061 | G | A | 1 | a0008c0008t0002g0232 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.543+1338G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091061 | |||||||
| chr2:58091122 | T | G | 1 | a0006c0010t0001g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.543+1399T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091122 | |||||||
| chr2:58091221 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.543+1498A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091221 | |||||||
| chr2:58091246 | A | G | 1 | a0001c0001t0002g0180 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.543+1523A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091246 | |||||||
| chr2:58091263 | A | C | 25 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(22): Show |
25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+1540A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091263 | |||||||
| chr2:58091566 | AAAATGTA others(4254): Show |
A | 1 | a0002c0002t0002g0273 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.543+1846_543+6106d others(2): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58091566 | ||||||
| chr2:58091688 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0326 a0001c0001t0002g0214 |
3 | HG00735.hp2 HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.543+1965C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091688 | |||||||
| chr2:58091689 | G | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.543+1966G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58091689 | |||||||
| chr2:58092321 | T | C | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+2598T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092321 | |||||||
| chr2:58092429 | G | A | 2 | a0002c0002t0002g0151 a0002c0002t0002g0154 |
2 | NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.543+2706G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092429 | |||||||
| chr2:58092480 | T | C | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.543+2757T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092480 | |||||||
| chr2:58092545 | A | C | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+2822A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092545 | |||||||
| chr2:58092629 | T | C | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.543+2906T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092629 | |||||||
| chr2:58092642 | A | T | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.543+2919A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092642 | |||||||
| chr2:58092729 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0327 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.543+3006A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58092729 | |||||||
| chr2:58093026 | G | GTA | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+3309_543+3310d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58093026 | ||||||
| chr2:58093121 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.543+3398C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093121 | |||||||
| chr2:58093321 | G | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | NA18977.hp2 NA19060.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.543+3598G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093321 | |||||||
| chr2:58093380 | A | G | 5 | a0001c0003t0001g0012 a0001c0003t0001g0015 a0001c0003t0004g0011 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+3657A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093380 | |||||||
| chr2:58093476 | C | G | 2 | a0001c0001t0001g0248 a0001c0001t0001g0250 |
2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.543+3753C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093476 | |||||||
| chr2:58093544 | T | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.543+3821T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093544 | |||||||
| chr2:58093663 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.543+3940G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093663 | |||||||
| chr2:58093670 | T | G | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+3947T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093670 | |||||||
| chr2:58093694 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.543+3971T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093694 | |||||||
| chr2:58093723 | T | A | 2 | a0002c0002t0002g0151 a0002c0002t0002g0154 |
2 | NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.543+4000T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093723 | |||||||
| chr2:58093993 | C | T | 4 | a0001c0003t0001g0267 a0001c0003t0001g0270 a0001c0003t0001g0271 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+4270C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58093993 | |||||||
| chr2:58094012 | C | G | 2 | a0001c0001t0002g0238 a0001c0001t0002g0239 |
2 | NA18992.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.543+4289C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58094012 | |||||||
| chr2:58094166 | A | G | 15 | a0001c0001t0001g0017 a0001c0001t0001g0142 a0001c0001t0001g0143 others(12): Show |
15 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.543+4443A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58094166 | |||||||
| chr2:58094370 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.543+4647A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58094370 | |||||||
| chr2:58094574 | G | C | 2 | a0002c0002t0002g0074 a0002c0002t0002g0112 |
2 | HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.543+4851G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58094574 | |||||||
| chr2:58094898 | T | G | 3 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0006c0010t0001g0148 |
3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.543+5175T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58094898 | |||||||
| chr2:58094917 | G | A | 24 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(21): Show |
24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.543+5194G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58094917 | |||||||
| chr2:58095022 | G | A | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+5299G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095022 | |||||||
| chr2:58095091 | A | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.543+5368A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095091 | |||||||
| chr2:58095092 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.543+5369G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095092 | |||||||
| chr2:58095154 | C | T | 1 | a0001c0003t0001g0015 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.543+5431C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095154 | |||||||
| chr2:58095166 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.543+5443T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095166 | |||||||
| chr2:58095226 | G | A | 1 | a0004c0007t0002g0218 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.543+5503G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095226 | |||||||
| chr2:58095293 | C | CAAAAA | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+5585_543+5589d others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58095293 | ||||||
| chr2:58095293 | C | CAAAAAAA others(2): Show |
9 | a0001c0001t0002g0016 a0001c0003t0001g0261 a0001c0003t0001g0263 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+5581_543+5589d others(11): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58095293 | ||||||
| chr2:58095340 | T | C | 15 | a0001c0001t0001g0017 a0001c0001t0001g0142 a0001c0001t0001g0143 others(12): Show |
15 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.543+5617T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095340 | |||||||
| chr2:58095457 | A | G | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+5734A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095457 | |||||||
| chr2:58095524 | T | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0088 |
3 | HG01928.hp2 HG01934.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.543+5801T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095524 | |||||||
| chr2:58095606 | A | G | 1 | a0001c0001t0002g0199 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.543+5883A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095606 | |||||||
| chr2:58095710 | A | G | 1 | a0002c0002t0002g0078 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.543+5987A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095710 | |||||||
| chr2:58095898 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.543+6175A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095898 | |||||||
| chr2:58095983 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.543+6260T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095983 | |||||||
| chr2:58095984 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.543+6261G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58095984 | |||||||
| chr2:58096053 | A | C | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.543+6330A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096053 | |||||||
| chr2:58096196 | A | T | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+6473A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096196 | |||||||
| chr2:58096236 | T | C | 1 | a0002c0002t0002g0064 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.543+6513T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096236 | |||||||
| chr2:58096420 | T | A | 1 | a0002c0002t0002g0081 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.543+6697T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096420 | |||||||
| chr2:58096591 | A | G | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+6868A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096591 | |||||||
| chr2:58096789 | A | G | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+7066A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096789 | |||||||
| chr2:58096824 | A | G | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+7101A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58096824 | |||||||
| chr2:58097261 | G | A | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.543+7538G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097261 | |||||||
| chr2:58097279 | TTCTC | T | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.543+7560_543+7563d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58097279 | ||||||
| chr2:58097404 | C | A | 3 | a0001c0003t0001g0267 a0001c0003t0001g0270 a0001c0003t0001g0272 |
3 | HG01884.hp2 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.543+7681C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097404 | |||||||
| chr2:58097410 | G | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(72): Show |
77 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.543+7687G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097410 | |||||||
| chr2:58097467 | A | G | 25 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(22): Show |
25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+7744A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097467 | |||||||
| chr2:58097589 | T | G | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+7866T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097589 | |||||||
| chr2:58097645 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.543+7922A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097645 | |||||||
| chr2:58097718 | T | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.543+7995T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097718 | |||||||
| chr2:58097827 | CTA | C | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+8106_543+8107d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58097827 | ||||||
| chr2:58097896 | TA | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(44): Show |
49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.543+8182delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58097896 | ||||||
| chr2:58097958 | T | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.543+8235T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097958 | |||||||
| chr2:58097992 | T | C | 2 | a0001c0001t0001g0259 a0001c0001t0001g0327 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.543+8269T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097992 | |||||||
| chr2:58097997 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.543+8274T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58097997 | |||||||
| chr2:58098065 | T | G | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+8342T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58098065 | |||||||
| chr2:58098159 | G | A | 25 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(22): Show |
25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+8436G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58098159 | |||||||
| chr2:58098241 | T | A | 1 | a0002c0002t0002g0066 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.543+8518T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58098241 | |||||||
| chr2:58098510 | T | G | 21 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(18): Show |
21 | HG00423.hp2 HG00735.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.543+8787T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58098510 | |||||||
| chr2:58098610 | A | AGCC | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.543+8888_543+8890d others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58098610 | ||||||
| chr2:58098665 | T | C | 2 | a0001c0001t0001g0259 a0001c0001t0001g0327 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.543+8942T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58098665 | |||||||
| chr2:58099245 | T | G | 25 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(22): Show |
25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+9522T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099245 | |||||||
| chr2:58099279 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.543+9556G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099279 | |||||||
| chr2:58099293 | T | C | 2 | a0002c0002t0002g0082 a0008c0008t0002g0232 |
2 | NA18986.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.543+9570T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099293 | |||||||
| chr2:58099313 | A | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.543+9590A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099313 | |||||||
| chr2:58099343 | A | G | 1 | a0001c0001t0002g0005 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.543+9620A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099343 | |||||||
| chr2:58099588 | T | G | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+9865T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099588 | |||||||
| chr2:58099609 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.543+9886G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099609 | |||||||
| chr2:58099735 | C | G | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+10012C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099735 | |||||||
| chr2:58099750 | T | A | 16 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(13): Show |
16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.543+10027T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099750 | |||||||
| chr2:58099751 | T | G | 1 | a0001c0001t0002g0174 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.543+10028T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099751 | |||||||
| chr2:58099797 | C | T | 1 | a0001c0001t0002g0018 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.543+10074C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58099797 | |||||||
| chr2:58100102 | A | G | 1 | a0002c0002t0002g0035 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.543+10379A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100102 | |||||||
| chr2:58100235 | G | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.543+10512G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100235 | |||||||
| chr2:58100333 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.543+10610A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100333 | |||||||
| chr2:58100335 | A | G | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.543+10612A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100335 | |||||||
| chr2:58100524 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.543+10801C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100524 | |||||||
| chr2:58100554 | T | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.543+10831T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100554 | |||||||
| chr2:58100614 | ATATTT | A | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+10895_543+1089 others(9): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58100614 | ||||||
| chr2:58100734 | A | G | 3 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0006c0010t0001g0148 |
3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.543+11011A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100734 | |||||||
| chr2:58100847 | A | C | 2 | a0001c0001t0002g0209 a0001c0001t0002g0217 |
2 | HG02015.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.543+11124A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100847 | |||||||
| chr2:58100983 | T | G | 1 | a0001c0001t0001g0307 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.543+11260T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58100983 | |||||||
| chr2:58101051 | TAG | T | 3 | a0001c0003t0001g0256 a0001c0003t0001g0257 a0001c0003t0001g0258 |
3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.543+11331_543+1133 others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58101051 | ||||||
| chr2:58101108 | A | G | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+11385A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101108 | |||||||
| chr2:58101115 | T | C | 4 | a0001c0001t0002g0182 a0001c0001t0002g0212 a0001c0001t0002g0213 others(1): Show |
4 | HG02027.hp2 HG02074.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+11392T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101115 | |||||||
| chr2:58101211 | A | G | 25 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(22): Show |
25 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+11488A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101211 | |||||||
| chr2:58101317 | T | G | 1 | a0001c0001t0001g0302 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.543+11594T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101317 | |||||||
| chr2:58101598 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.543+11875T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101598 | |||||||
| chr2:58101746 | G | T | 1 | a0001c0001t0001g0280 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.543+12023G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101746 | |||||||
| chr2:58101762 | G | A | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+12039G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101762 | |||||||
| chr2:58101855 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.543+12132T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101855 | |||||||
| chr2:58101908 | T | C | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.543+12185T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101908 | |||||||
| chr2:58101950 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.543+12227A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101950 | |||||||
| chr2:58101993 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.543+12270G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58101993 | |||||||
| chr2:58102118 | T | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0275 |
4 | NA18945.hp1 NA18952.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+12395T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102118 | |||||||
| chr2:58102320 | T | A | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+12597T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102320 | |||||||
| chr2:58102321 | A | T | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+12598A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102321 | |||||||
| chr2:58102337 | A | G | 12 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(9): Show |
12 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.543+12614A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102337 | |||||||
| chr2:58102376 | A | T | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+12653A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102376 | |||||||
| chr2:58102406 | A | C | 1 | a0001c0001t0002g0185 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.543+12683A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102406 | |||||||
| chr2:58102492 | T | TA | 43 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(40): Show |
46 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.543+12784dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58102492 | ||||||
| chr2:58102570 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.543+12847A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102570 | |||||||
| chr2:58102646 | A | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.543+12923A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102646 | |||||||
| chr2:58102782 | C | T | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+13059C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102782 | |||||||
| chr2:58102818 | T | C | 11 | a0001c0001t0002g0172 a0001c0001t0002g0214 a0001c0001t0002g0215 others(8): Show |
11 | HG00735.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.543+13095T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102818 | |||||||
| chr2:58102866 | T | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
9 | NA18943.hp2 NA18947.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+13143T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102866 | |||||||
| chr2:58102979 | G | A | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+13256G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58102979 | |||||||
| chr2:58103583 | C | T | 19 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(16): Show |
19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.543+13860C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58103583 | |||||||
| chr2:58103614 | C | T | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.543+13891C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58103614 | |||||||
| chr2:58103637 | A | G | 21 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(18): Show |
21 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.543+13914A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58103637 | |||||||
| chr2:58103947 | C | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0264 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.543+14224C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58103947 | |||||||
| chr2:58103969 | A | G | 2 | a0002c0002t0002g0084 a0002c0002t0005g0109 |
2 | NA19012.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.543+14246A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58103969 | |||||||
| chr2:58104006 | T | C | 1 | a0001c0001t0002g0221 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.543+14283T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104006 | |||||||
| chr2:58104076 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.543+14353A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104076 | |||||||
| chr2:58104250 | T | A | 1 | a0002c0002t0002g0037 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.543+14527T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104250 | |||||||
| chr2:58104382 | A | G | 1 | a0006c0010t0001g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.543+14659A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104382 | |||||||
| chr2:58104405 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.543+14682C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104405 | |||||||
| chr2:58104458 | TACAGTA | T | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+14738_543+1474 others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58104458 | ||||||
| chr2:58104497 | T | G | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+14774T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104497 | |||||||
| chr2:58104576 | A | G | 1 | a0001c0003t0001g0010 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.543+14853A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104576 | |||||||
| chr2:58104660 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.543+14937T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104660 | |||||||
| chr2:58104767 | A | G | 4 | a0001c0001t0002g0191 a0001c0001t0002g0196 a0001c0001t0002g0206 others(1): Show |
4 | HG00408.hp2 HG02155.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+15044A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104767 | |||||||
| chr2:58104909 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.543+15186A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58104909 | |||||||
| chr2:58105066 | G | A | 1 | a0002c0002t0002g0030 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.543+15343G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58105066 | |||||||
| chr2:58105399 | T | C | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+15676T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58105399 | |||||||
| chr2:58105622 | A | C | 26 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(23): Show |
26 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.543+15899A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58105622 | |||||||
| chr2:58105726 | G | T | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+16003G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58105726 | |||||||
| chr2:58105856 | T | G | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+16133T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58105856 | |||||||
| chr2:58106037 | T | G | 1 | a0001c0001t0002g0199 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.543+16314T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106037 | |||||||
| chr2:58106092 | C | T | 1 | a0001c0003t0001g0015 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.543+16369C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106092 | |||||||
| chr2:58106155 | T | C | 1 | a0002c0002t0002g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.543+16432T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106155 | |||||||
| chr2:58106158 | A | G | 1 | a0002c0002t0002g0226 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.543+16435A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106158 | |||||||
| chr2:58106170 | G | GT | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+16453dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58106170 | ||||||
| chr2:58106183 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.543+16460A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106183 | |||||||
| chr2:58106320 | C | G | 12 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(9): Show |
12 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.543+16597C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106320 | |||||||
| chr2:58106422 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.544-16679G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106422 | |||||||
| chr2:58106578 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.544-16523A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106578 | |||||||
| chr2:58106636 | T | G | 1 | a0001c0001t0002g0005 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.544-16465T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106636 | |||||||
| chr2:58106692 | T | C | 19 | a0001c0001t0001g0144 a0001c0001t0001g0259 a0001c0001t0001g0309 others(16): Show |
19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-16409T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58106692 | |||||||
| chr2:58106751 | CAG | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.544-16348_544-1634 others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58106751 | ||||||
| chr2:58107095 | T | TG | 21 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(18): Show |
21 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.544-16005dupG | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58107095 | ||||||
| chr2:58107104 | G | A | 24 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(21): Show |
24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.544-15997G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107104 | |||||||
| chr2:58107113 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-15988T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107113 | |||||||
| chr2:58107151 | AT | A | 24 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(21): Show |
24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.544-15949delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107151 | |||||||
| chr2:58107472 | T | A | 21 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(18): Show |
21 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.544-15629T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107472 | |||||||
| chr2:58107492 | CTTCCTAG others(7): Show |
C | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.544-15605_544-1559 others(18): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58107492 | ||||||
| chr2:58107516 | C | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-15585C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107516 | |||||||
| chr2:58107531 | T | C | 21 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(18): Show |
21 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.544-15570T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107531 | |||||||
| chr2:58107646 | A | T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0208 a0001c0001t0006g0207 |
3 | HG02083.hp1 NA19056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.544-15455A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107646 | |||||||
| chr2:58107664 | A | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(318): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.544-15437A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107664 | |||||||
| chr2:58107664 | A | G | 2 | a0001c0001t0002g0008 a0001c0001t0002g0186 |
3 | HG01099.hp1 HG01106.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.544-15437A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107664 | |||||||
| chr2:58107734 | A | G | 21 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(18): Show |
21 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.544-15367A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107734 | |||||||
| chr2:58107773 | C | T | 19 | a0001c0001t0001g0144 a0001c0001t0001g0259 a0001c0001t0001g0309 others(16): Show |
19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-15328C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107773 | |||||||
| chr2:58107790 | A | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(324): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.544-15311A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107790 | |||||||
| chr2:58107851 | A | G | 3 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0002g0217 |
3 | HG00558.hp1 HG02015.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.544-15250A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107851 | |||||||
| chr2:58107900 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.544-15201C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107900 | |||||||
| chr2:58107940 | G | T | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.544-15161G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107940 | |||||||
| chr2:58107946 | G | C | 1 | a0001c0001t0001g0292 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.544-15155G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58107946 | |||||||
| chr2:58108043 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.544-15058C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108043 | |||||||
| chr2:58108051 | C | G | 22 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(19): Show |
22 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.544-15050C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108051 | |||||||
| chr2:58108084 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.544-15017A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108084 | |||||||
| chr2:58108320 | T | A | 19 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(16): Show |
19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-14781T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108320 | |||||||
| chr2:58108422 | C | T | 1 | a0001c0001t0002g0005 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.544-14679C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108422 | |||||||
| chr2:58108522 | T | C | 17 | a0001c0001t0001g0144 a0001c0001t0001g0259 a0001c0001t0001g0311 others(14): Show |
17 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.544-14579T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108522 | |||||||
| chr2:58108546 | T | C | 89 | a0002c0002t0001g0025 a0002c0002t0001g0149 a0002c0002t0001g0150 others(86): Show |
90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.544-14555T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108546 | |||||||
| chr2:58108621 | C | G | 25 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0052 others(22): Show |
25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.544-14480C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108621 | |||||||
| chr2:58108745 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-14356C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108745 | |||||||
| chr2:58108940 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.544-14161A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108940 | |||||||
| chr2:58108999 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(109): Show |
114 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.544-14102C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58108999 | |||||||
| chr2:58109082 | TGCTTGGC others(17): Show |
T | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-13994_544-1397 others(28): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58109082 | ||||||
| chr2:58109091 | C | T | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.544-14010C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109091 | |||||||
| chr2:58109149 | G | T | 22 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(19): Show |
22 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.544-13952G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109149 | |||||||
| chr2:58109226 | T | C | 21 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(18): Show |
21 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.544-13875T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109226 | |||||||
| chr2:58109393 | T | C | 1 | a0001c0001t0002g0221 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.544-13708T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109393 | |||||||
| chr2:58109434 | GA | G | 8 | a0001c0001t0001g0119 a0001c0001t0001g0158 a0001c0001t0001g0159 others(5): Show |
8 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-13654delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58109434 | ||||||
| chr2:58109579 | A | G | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.544-13522A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109579 | |||||||
| chr2:58109676 | G | A | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-13425G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109676 | |||||||
| chr2:58109875 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.544-13226A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109875 | |||||||
| chr2:58109967 | G | C | 1 | a0002c0002t0002g0030 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.544-13134G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58109967 | |||||||
| chr2:58110012 | A | G | 2 | a0001c0001t0002g0208 a0001c0001t0006g0207 |
2 | HG02083.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.544-13089A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110012 | |||||||
| chr2:58110055 | T | C | 1 | a0002c0002t0002g0273 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.544-13046T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110055 | |||||||
| chr2:58110192 | T | C | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.544-12909T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110192 | |||||||
| chr2:58110400 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-12701C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110400 | |||||||
| chr2:58110572 | C | T | 1 | a0001c0003t0001g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.544-12529C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110572 | |||||||
| chr2:58110860 | A | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-12241A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110860 | |||||||
| chr2:58110925 | C | G | 3 | a0001c0001t0002g0167 a0001c0001t0002g0208 a0001c0001t0006g0207 |
3 | HG02083.hp1 NA19056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.544-12176C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110925 | |||||||
| chr2:58110951 | A | G | 93 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(90): Show |
94 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.544-12150A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58110951 | |||||||
| chr2:58111012 | A | C | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-12089A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111012 | |||||||
| chr2:58111035 | G | A | 1 | a0006c0010t0001g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.544-12066G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111035 | |||||||
| chr2:58111051 | A | C | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-12050A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111051 | |||||||
| chr2:58111073 | C | G | 12 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(9): Show |
12 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.544-12028C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111073 | |||||||
| chr2:58111110 | G | A | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.544-11991G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111110 | |||||||
| chr2:58111318 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.544-11783T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111318 | |||||||
| chr2:58111319 | C | A | 1 | a0001c0001t0001g0276 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.544-11782C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111319 | |||||||
| chr2:58111381 | A | C | 2 | a0001c0003t0001g0271 a0001c0003t0001g0272 |
2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.544-11720A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111381 | |||||||
| chr2:58111402 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.544-11699G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111402 | |||||||
| chr2:58111637 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.544-11464C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111637 | |||||||
| chr2:58111662 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.544-11439A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111662 | |||||||
| chr2:58111770 | G | A | 7 | a0001c0001t0003g0241 a0001c0001t0003g0242 a0001c0001t0003g0243 others(4): Show |
7 | HG01256.hp1 HG01258.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.544-11331G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111770 | |||||||
| chr2:58111823 | C | G | 3 | a0001c0001t0002g0167 a0001c0001t0002g0208 a0001c0001t0006g0207 |
3 | HG02083.hp1 NA19056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.544-11278C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58111823 | |||||||
| chr2:58112087 | G | T | 1 | a0001c0001t0001g0299 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.544-11014G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58112087 | |||||||
| chr2:58112148 | A | G | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-10953A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58112148 | |||||||
| chr2:58112442 | A | T | 26 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(23): Show |
26 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.544-10659A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58112442 | |||||||
| chr2:58112576 | G | GA | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(104): Show |
110 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.544-10513dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58112576 | ||||||
| chr2:58112576 | G | GAAA | 11 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.544-10515_544-1051 others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58112576 | ||||||
| chr2:58112584 | A | AG | 53 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(50): Show |
55 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.544-10517_544-1051 others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58112584 | |||||||
| chr2:58113182 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0275 |
4 | NA18945.hp1 NA18952.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-9919G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113182 | |||||||
| chr2:58113300 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-9801G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113300 | |||||||
| chr2:58113307 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0179 |
2 | HG00738.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.544-9794C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113307 | |||||||
| chr2:58113312 | C | CA | 28 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0057 others(25): Show |
28 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.544-9771dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58113312 | ||||||
| chr2:58113312 | CA | C | 22 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0001g0138 others(19): Show |
22 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.544-9771delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58113312 | ||||||
| chr2:58113394 | C | T | 1 | a0002c0002t0002g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.544-9707C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113394 | |||||||
| chr2:58113424 | A | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0283 |
2 | NA18949.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.544-9677A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113424 | |||||||
| chr2:58113596 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
9 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-9505A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113596 | |||||||
| chr2:58113648 | G | T | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-9453G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113648 | |||||||
| chr2:58113686 | G | A | 23 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(20): Show |
23 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.544-9415G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113686 | |||||||
| chr2:58113810 | C | G | 19 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(16): Show |
19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-9291C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113810 | |||||||
| chr2:58113833 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0326 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.544-9268G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113833 | |||||||
| chr2:58113863 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.544-9238C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113863 | |||||||
| chr2:58113890 | T | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-9211T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113890 | |||||||
| chr2:58113922 | C | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-9179C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113922 | |||||||
| chr2:58113937 | G | A | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-9164G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113937 | |||||||
| chr2:58113974 | T | C | 1 | a0001c0001t0001g0284 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.544-9127T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58113974 | |||||||
| chr2:58114244 | A | T | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG01243.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.544-8857A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114244 | |||||||
| chr2:58114272 | T | C | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8829T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114272 | |||||||
| chr2:58114284 | G | T | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8817G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114284 | |||||||
| chr2:58114292 | A | C | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8809A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114292 | |||||||
| chr2:58114308 | C | T | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8793C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114308 | |||||||
| chr2:58114318 | T | C | 1 | a0002c0002t0002g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.544-8783T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114318 | |||||||
| chr2:58114342 | A | G | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8759A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114342 | |||||||
| chr2:58114356 | G | A | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-8745G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114356 | |||||||
| chr2:58114382 | A | C | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-8719A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114382 | |||||||
| chr2:58114562 | C | G | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-8539C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114562 | |||||||
| chr2:58114569 | G | C | 15 | a0001c0001t0001g0017 a0001c0001t0001g0142 a0001c0001t0001g0143 others(12): Show |
15 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.544-8532G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114569 | |||||||
| chr2:58114615 | T | C | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-8486T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114615 | |||||||
| chr2:58114664 | C | T | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-8437C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114664 | |||||||
| chr2:58114672 | C | G | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8429C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114672 | |||||||
| chr2:58114673 | A | G | 18 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(15): Show |
18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-8428A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114673 | |||||||
| chr2:58114698 | A | AACC | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-8403_544-8402i others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114698 | |||||||
| chr2:58114703 | G | A | 19 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(16): Show |
19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-8398G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114703 | |||||||
| chr2:58114892 | C | G | 19 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(16): Show |
19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-8209C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58114892 | |||||||
| chr2:58115092 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-8009G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115092 | |||||||
| chr2:58115327 | A | G | 1 | a0002c0002t0001g0253 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.544-7774A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115327 | |||||||
| chr2:58115426 | A | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0031 others(8): Show |
11 | HG01928.hp2 HG01934.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-7675A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115426 | |||||||
| chr2:58115427 | C | T | 11 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0031 others(8): Show |
11 | HG01928.hp2 HG01934.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-7674C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115427 | |||||||
| chr2:58115444 | G | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0031 others(8): Show |
11 | HG01928.hp2 HG01934.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-7657G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115444 | |||||||
| chr2:58115496 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-7605G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115496 | |||||||
| chr2:58115513 | G | A | 3 | a0002c0002t0002g0273 a0002c0002t0002g0281 a0002c0002t0002g0282 |
3 | HG02698.hp2 HG03490.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.544-7588G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115513 | |||||||
| chr2:58115545 | ATTTG | A | 88 | a0001c0001t0001g0292 a0002c0002t0001g0025 a0002c0002t0001g0253 others(85): Show |
89 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.544-7551_544-7548d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58115545 | ||||||
| chr2:58115697 | C | G | 6 | a0001c0003t0001g0267 a0001c0003t0001g0268 a0001c0003t0001g0269 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-7404C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115697 | |||||||
| chr2:58115739 | GGATGAAA others(1): Show |
G | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-7361_544-7354d others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115739 | |||||||
| chr2:58115767 | C | T | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-7334C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115767 | |||||||
| chr2:58115785 | C | G | 3 | a0001c0003t0001g0256 a0001c0003t0001g0257 a0001c0003t0001g0258 |
3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.544-7316C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115785 | |||||||
| chr2:58115972 | C | T | 2 | a0001c0003t0001g0261 a0001c0003t0001g0263 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.544-7129C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58115972 | |||||||
| chr2:58116225 | G | A | 1 | a0002c0002t0002g0062 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.544-6876G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116225 | |||||||
| chr2:58116249 | A | C | 22 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(19): Show |
22 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.544-6852A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116249 | |||||||
| chr2:58116284 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.544-6817A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116284 | |||||||
| chr2:58116320 | C | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.544-6781C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116320 | |||||||
| chr2:58116336 | C | T | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-6765C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116336 | |||||||
| chr2:58116337 | G | A | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-6764G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116337 | |||||||
| chr2:58116341 | A | G | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-6760A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116341 | |||||||
| chr2:58116348 | G | A | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-6753G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116348 | |||||||
| chr2:58116401 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.544-6700G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116401 | |||||||
| chr2:58116429 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.544-6672A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116429 | |||||||
| chr2:58116436 | T | A | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-6665T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116436 | |||||||
| chr2:58116438 | A | C | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-6663A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116438 | |||||||
| chr2:58116443 | A | G | 5 | a0002c0002t0002g0044 a0002c0002t0002g0078 a0002c0002t0002g0081 others(2): Show |
5 | NA18966.hp1 NA18975.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-6658A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116443 | |||||||
| chr2:58116455 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.544-6646G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116455 | |||||||
| chr2:58116596 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.544-6505C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116596 | |||||||
| chr2:58116690 | C | T | 1 | a0002c0002t0002g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.544-6411C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116690 | |||||||
| chr2:58116769 | A | G | 2 | a0001c0003t0001g0267 a0001c0003t0001g0270 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.544-6332A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116769 | |||||||
| chr2:58116777 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.544-6324G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116777 | |||||||
| chr2:58116794 | C | T | 7 | a0002c0002t0002g0151 a0002c0002t0002g0152 a0002c0002t0002g0153 others(4): Show |
7 | HG00621.hp2 NA18961.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.544-6307C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116794 | |||||||
| chr2:58116795 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.544-6306G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116795 | |||||||
| chr2:58116885 | G | T | 1 | a0002c0002t0002g0034 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.544-6216G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116885 | |||||||
| chr2:58116941 | C | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-6160C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116941 | |||||||
| chr2:58116988 | G | A | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-6113G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58116988 | |||||||
| chr2:58117054 | G | A | 89 | a0002c0002t0001g0025 a0002c0002t0001g0149 a0002c0002t0001g0150 others(86): Show |
90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.544-6047G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117054 | |||||||
| chr2:58117093 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.544-6008G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117093 | |||||||
| chr2:58117181 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.544-5920G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117181 | |||||||
| chr2:58117418 | A | G | 18 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(15): Show |
18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-5683A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117418 | |||||||
| chr2:58117511 | G | T | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-5590G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117511 | |||||||
| chr2:58117514 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.544-5587G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117514 | |||||||
| chr2:58117657 | C | T | 18 | a0001c0001t0002g0005 a0001c0001t0002g0168 a0001c0001t0002g0174 others(15): Show |
19 | HG00280.hp2 HG00741.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-5444C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117657 | |||||||
| chr2:58117711 | G | A | 1 | a0002c0002t0002g0100 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.544-5390G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117711 | |||||||
| chr2:58117740 | T | G | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.544-5361T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117740 | |||||||
| chr2:58117748 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.544-5353A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117748 | |||||||
| chr2:58117751 | G | A | 24 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(21): Show |
24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.544-5350G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117751 | |||||||
| chr2:58117773 | C | T | 2 | a0001c0001t0003g0242 a0001c0001t0003g0243 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.544-5328C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117773 | |||||||
| chr2:58117852 | G | A | 1 | a0001c0001t0003g0246 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.544-5249G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117852 | |||||||
| chr2:58117946 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.544-5155G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58117946 | |||||||
| chr2:58118006 | A | C | 24 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(21): Show |
24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.544-5095A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118006 | |||||||
| chr2:58118090 | C | T | 11 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0031 others(8): Show |
11 | HG01928.hp2 HG01934.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-5011C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118090 | |||||||
| chr2:58118122 | A | G | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0006c0010t0001g0148 |
3 | HG02559.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.544-4979A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118122 | |||||||
| chr2:58118258 | A | T | 1 | a0002c0002t0002g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.544-4843A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118258 | |||||||
| chr2:58118301 | C | T | 1 | a0002c0002t0002g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.544-4800C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118301 | |||||||
| chr2:58118315 | C | T | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-4786C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118315 | |||||||
| chr2:58118337 | T | C | 4 | a0001c0003t0001g0267 a0001c0003t0001g0270 a0001c0003t0001g0271 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-4764T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118337 | |||||||
| chr2:58118360 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.544-4741G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118360 | |||||||
| chr2:58118381 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(46): Show |
51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.544-4720C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118381 | |||||||
| chr2:58118392 | G | T | 12 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(9): Show |
12 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.544-4709G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118392 | |||||||
| chr2:58118397 | T | C | 18 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(15): Show |
18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-4704T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118397 | |||||||
| chr2:58118473 | T | A | 1 | a0001c0001t0002g0169 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.544-4628T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118473 | |||||||
| chr2:58118553 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.544-4548G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118553 | |||||||
| chr2:58118607 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.544-4494C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118607 | |||||||
| chr2:58118679 | TC | T | 12 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(9): Show |
12 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.544-4420delC | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58118679 | ||||||
| chr2:58118682 | G | A | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-4419G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118682 | |||||||
| chr2:58118779 | G | A | 3 | a0002c0002t0002g0067 a0002c0002t0002g0068 a0002c0002t0002g0288 |
3 | HG01516.hp2 HG02258.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.544-4322G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118779 | |||||||
| chr2:58118884 | T | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(19): Show |
25 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.544-4217T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118884 | |||||||
| chr2:58118975 | G | C | 3 | a0001c0001t0001g0216 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | NA18977.hp2 NA19060.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.544-4126G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58118975 | |||||||
| chr2:58119026 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.544-4075C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119026 | |||||||
| chr2:58119099 | C | T | 1 | a0002c0002t0002g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.544-4002C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119099 | |||||||
| chr2:58119234 | A | C | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-3867A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119234 | |||||||
| chr2:58119300 | C | A | 1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.544-3801C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119300 | |||||||
| chr2:58119309 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.544-3792C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119309 | |||||||
| chr2:58119343 | C | CA | 12 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0015 others(9): Show |
12 | HG01168.hp2 HG01891.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.544-3742dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58119343 | ||||||
| chr2:58119343 | CA | C | 28 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0105 others(25): Show |
28 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.544-3742delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58119343 | ||||||
| chr2:58119376 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.544-3725C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119376 | |||||||
| chr2:58119409 | G | A | 8 | a0002c0002t0002g0224 a0002c0002t0002g0226 a0002c0002t0002g0227 others(5): Show |
8 | HG02027.hp1 HG02040.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-3692G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119409 | |||||||
| chr2:58119426 | G | A | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-3675G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119426 | |||||||
| chr2:58119476 | C | CA | 100 | a0001c0001t0001g0089 a0001c0001t0001g0133 a0001c0001t0001g0140 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.544-3607dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58119476 | ||||||
| chr2:58119476 | C | CAA | 8 | a0002c0002t0001g0025 a0002c0002t0002g0028 a0002c0002t0002g0037 others(5): Show |
8 | HG01168.hp2 HG01255.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-3608_544-3607d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58119476 | ||||||
| chr2:58119583 | G | A | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-3518G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119583 | |||||||
| chr2:58119665 | C | T | 1 | a0002c0002t0002g0063 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.544-3436C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119665 | |||||||
| chr2:58119830 | A | G | 2 | a0001c0001t0001g0216 a0001c0001t0001g0236 |
2 | NA19060.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.544-3271A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119830 | |||||||
| chr2:58119831 | A | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.544-3270A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119831 | |||||||
| chr2:58119952 | A | T | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-3149A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58119952 | |||||||
| chr2:58120076 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.544-3025T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120076 | |||||||
| chr2:58120179 | CTTTTCTT others(6): Show |
C | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-2917_544-2905d others(15): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120179 | ||||||
| chr2:58120179 | CTTTTCTT others(7): Show |
C | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-2917_544-2904d others(16): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120179 | ||||||
| chr2:58120184 | C | CT | 6 | a0001c0001t0001g0032 a0001c0001t0001g0106 a0001c0001t0002g0192 others(3): Show |
6 | HG00423.hp1 HG00558.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-2893dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTCTTT others(15): Show |
1 | a0001c0001t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544-2914_544-2913i others(24): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0324 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.544-2902_544-2893d others(12): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(4): Show |
6 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-2903_544-2893d others(13): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(5): Show |
5 | a0001c0001t0001g0278 a0001c0001t0001g0296 a0001c0001t0001g0297 others(2): Show |
5 | HG03041.hp1 HG03540.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-2904_544-2893d others(14): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0279 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | HG02109.hp1 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-2905_544-2893d others(15): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(7): Show |
9 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0176 others(6): Show |
10 | HG02145.hp1 HG03453.hp2 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-2906_544-2893d others(16): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(8): Show |
11 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0049 others(8): Show |
11 | HG02738.hp1 HG03209.hp2 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-2907_544-2893d others(17): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(9): Show |
16 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0050 others(13): Show |
16 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.544-2908_544-2893d others(18): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(10): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0048 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.544-2909_544-2893d others(19): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(11): Show |
14 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0125 others(11): Show |
15 | HG00280.hp1 HG01975.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.544-2910_544-2893d others(20): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(12): Show |
2 | a0001c0001t0001g0291 a0001c0004t0001g0132 |
2 | HG00438.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.544-2911_544-2893d others(21): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(13): Show |
2 | a0001c0004t0001g0130 a0001c0004t0001g0131 |
2 | HG02004.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.544-2912_544-2893d others(22): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(15): Show |
4 | a0001c0001t0001g0023 a0001c0001t0001g0163 a0001c0001t0001g0285 others(1): Show |
4 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-2914_544-2893d others(24): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(17): Show |
2 | a0001c0001t0001g0160 a0001c0001t0001g0162 |
2 | HG02280.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.544-2916_544-2893d others(26): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(18): Show |
5 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-2893_544-2892i others(27): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.544-2893_544-2892i others(29): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0001g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.544-2893_544-2892i others(32): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | CT | C | 82 | a0001c0001t0002g0172 a0001c0001t0002g0214 a0001c0001t0002g0215 others(79): Show |
83 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.544-2893delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120184 | CTT | C | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-2894_544-2893d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 58120184 | ||||||
| chr2:58120191 | T | C | 1 | a0001c0001t0002g0005 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.544-2910T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120191 | |||||||
| chr2:58120301 | C | T | 19 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0259 others(16): Show |
19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-2800C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120301 | |||||||
| chr2:58120420 | A | T | 2 | a0001c0003t0001g0261 a0001c0003t0001g0263 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.544-2681A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120420 | |||||||
| chr2:58120637 | C | T | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-2464C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120637 | |||||||
| chr2:58120707 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(106): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.544-2394T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120707 | |||||||
| chr2:58120794 | T | C | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-2307T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120794 | |||||||
| chr2:58120810 | C | A | 24 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(21): Show |
24 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.544-2291C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58120810 | |||||||
| chr2:58121230 | T | G | 1 | a0001c0001t0001g0292 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.544-1871T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58121230 | |||||||
| chr2:58121340 | G | A | 19 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(16): Show |
19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.544-1761G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58121340 | |||||||
| chr2:58121487 | C | T | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-1614C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58121487 | |||||||
| chr2:58121548 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-1553A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58121548 | |||||||
| chr2:58121592 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-1509A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58121592 | |||||||
| chr2:58121888 | T | C | 1 | a0001c0001t0001g0004 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.544-1213T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58121888 | |||||||
| chr2:58122132 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.544-969T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122132 | |||||||
| chr2:58122698 | C | G | 1 | a0002c0002t0002g0033 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.544-403C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122698 | |||||||
| chr2:58122766 | C | T | 1 | a0002c0002t0002g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.544-335C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122766 | |||||||
| chr2:58122767 | T | G | 1 | a0002c0002t0002g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.544-334T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122767 | |||||||
| chr2:58122769 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.544-332C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122769 | |||||||
| chr2:58122772 | A | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.544-329A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122772 | |||||||
| chr2:58122782 | A | G | 1 | a0002c0002t0002g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.544-319A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122782 | |||||||
| chr2:58122822 | T | C | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-279T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122822 | |||||||
| chr2:58122830 | T | G | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-271T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122830 | |||||||
| chr2:58122925 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.544-176G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | chr2 | 58122925 | |||||||
| chr2:58123369 | A | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(316): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.676+136A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123369 | |||||||
| chr2:58123388 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.676+155A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123388 | |||||||
| chr2:58123397 | T | C | 26 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(23): Show |
26 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.676+164T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123397 | |||||||
| chr2:58123436 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.676+203G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123436 | |||||||
| chr2:58123533 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.676+300A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123533 | |||||||
| chr2:58123771 | C | G | 1 | a0001c0003t0001g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.676+538C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123771 | |||||||
| chr2:58123853 | GA | G | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.676+634delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 58123853 | ||||||
| chr2:58123862 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.676+629A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123862 | |||||||
| chr2:58123936 | C | G | 1 | a0002c0002t0002g0077 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.676+703C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123936 | |||||||
| chr2:58123955 | T | G | 1 | a0001c0001t0001g0280 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.676+722T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58123955 | |||||||
| chr2:58124308 | C | T | 1 | a0002c0002t0001g0045 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.676+1075C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58124308 | |||||||
| chr2:58124552 | C | G | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.676+1319C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58124552 | |||||||
| chr2:58124793 | G | A | 1 | a0001c0003t0001g0009 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.676+1560G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58124793 | |||||||
| chr2:58124796 | A | G | 5 | a0001c0001t0002g0040 a0001c0001t0002g0192 a0001c0001t0002g0200 others(2): Show |
5 | HG02071.hp1 HG02165.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+1563A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58124796 | |||||||
| chr2:58124914 | T | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0178 |
2 | NA18961.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.676+1681T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58124914 | |||||||
| chr2:58124924 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.676+1691G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58124924 | |||||||
| chr2:58125049 | A | T | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.676+1816A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125049 | |||||||
| chr2:58125119 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.676+1886G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125119 | |||||||
| chr2:58125316 | A | G | 1 | a0001c0003t0001g0271 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676+2083A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125316 | |||||||
| chr2:58125456 | T | A | 1 | a0006c0010t0001g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.676+2223T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125456 | |||||||
| chr2:58125551 | T | G | 1 | a0002c0002t0002g0227 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.676+2318T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125551 | |||||||
| chr2:58125613 | G | GT | 11 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.676+2384dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 58125613 | ||||||
| chr2:58125741 | T | G | 2 | a0001c0001t0002g0233 a0001c0001t0002g0234 |
2 | NA18991.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.676+2508T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125741 | |||||||
| chr2:58125762 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.676+2529A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125762 | |||||||
| chr2:58125890 | A | G | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.676+2657A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58125890 | |||||||
| chr2:58126121 | T | C | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.676+2888T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126121 | |||||||
| chr2:58126129 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.676+2896A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126129 | |||||||
| chr2:58126141 | A | G | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.676+2908A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126141 | |||||||
| chr2:58126259 | A | G | 1 | a0001c0003t0001g0270 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.676+3026A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126259 | |||||||
| chr2:58126377 | TTTCTATG others(13): Show |
T | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.676+3146_676+3165d others(22): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 58126377 | ||||||
| chr2:58126450 | C | G | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+3217C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126450 | |||||||
| chr2:58126475 | A | G | 18 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(15): Show |
18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.676+3242A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126475 | |||||||
| chr2:58126541 | TGATG | T | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.676+3315_676+3318d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 58126541 | ||||||
| chr2:58126543 | A | G | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.676+3310A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126543 | |||||||
| chr2:58126578 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.676+3345T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126578 | |||||||
| chr2:58126602 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.676+3369A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126602 | |||||||
| chr2:58126651 | C | T | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.676+3418C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126651 | |||||||
| chr2:58126665 | A | G | 2 | a0001c0003t0001g0009 a0001c0003t0001g0010 |
2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.676+3432A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126665 | |||||||
| chr2:58126930 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.676+3697C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58126930 | |||||||
| chr2:58127150 | T | A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.676+3917T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127150 | |||||||
| chr2:58127229 | G | A | 3 | a0001c0001t0002g0167 a0001c0001t0002g0208 a0001c0001t0006g0207 |
3 | HG02083.hp1 NA19056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.676+3996G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127229 | |||||||
| chr2:58127249 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.676+4016T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127249 | |||||||
| chr2:58127287 | A | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.676+4054A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127287 | |||||||
| chr2:58127298 | A | G | 1 | a0001c0001t0002g0167 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.676+4065A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127298 | |||||||
| chr2:58127417 | C | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.676+4184C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127417 | |||||||
| chr2:58127421 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.676+4188A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127421 | |||||||
| chr2:58127799 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.677-4009C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127799 | |||||||
| chr2:58127836 | G | A | 87 | a0002c0002t0001g0025 a0002c0002t0001g0253 a0002c0002t0002g0003 others(84): Show |
88 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.677-3972G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127836 | |||||||
| chr2:58127863 | T | C | 8 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(5): Show |
8 | HG02735.hp2 HG02738.hp1 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.677-3945T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58127863 | |||||||
| chr2:58128077 | T | G | 27 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(24): Show |
27 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.677-3731T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128077 | |||||||
| chr2:58128144 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.677-3664T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128144 | |||||||
| chr2:58128144 | T | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.677-3664T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128144 | |||||||
| chr2:58128172 | G | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0264 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.677-3636G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128172 | |||||||
| chr2:58128441 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.677-3367C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128441 | |||||||
| chr2:58128566 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.677-3242A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128566 | |||||||
| chr2:58128751 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.677-3057C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128751 | |||||||
| chr2:58128892 | G | A | 5 | a0002c0002t0002g0084 a0002c0002t0002g0085 a0002c0002t0002g0099 others(2): Show |
5 | NA18943.hp1 NA18951.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-2916G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58128892 | |||||||
| chr2:58129244 | A | C | 1 | a0001c0001t0002g0169 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.677-2564A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58129244 | |||||||
| chr2:58129525 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.677-2283A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58129525 | |||||||
| chr2:58129526 | T | A | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.677-2282T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58129526 | |||||||
| chr2:58129692 | T | C | 12 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.677-2116T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58129692 | |||||||
| chr2:58129920 | G | T | 13 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(10): Show |
13 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-1888G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58129920 | |||||||
| chr2:58130151 | A | G | 1 | a0001c0003t0001g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.677-1657A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58130151 | |||||||
| chr2:58130437 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.677-1371G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58130437 | |||||||
| chr2:58130471 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.677-1337G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58130471 | |||||||
| chr2:58130710 | T | C | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.677-1098T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58130710 | |||||||
| chr2:58131102 | G | T | 1 | a0002c0002t0002g0254 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.677-706G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131102 | |||||||
| chr2:58131361 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.677-447A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131361 | |||||||
| chr2:58131368 | G | A | 1 | a0003c0005t0001g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.677-440G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131368 | |||||||
| chr2:58131373 | C | T | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.677-435C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131373 | |||||||
| chr2:58131398 | A | G | 1 | a0002c0002t0001g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.677-410A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131398 | |||||||
| chr2:58131441 | G | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
8 | HG00423.hp2 HG02040.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.677-367G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131441 | |||||||
| chr2:58131534 | G | A | 3 | a0001c0003t0001g0256 a0001c0003t0001g0257 a0001c0003t0001g0258 |
3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.677-274G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131534 | |||||||
| chr2:58131605 | A | G | 1 | a0002c0002t0002g0230 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.677-203A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131605 | |||||||
| chr2:58131675 | C | G | 21 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(18): Show |
21 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.677-133C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131675 | |||||||
| chr2:58131693 | C | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.677-115C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 8/12 | chr2 | 58131693 | |||||||
| chr2:58131935 | A | T | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.797+7A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58131935 | |||||||
| chr2:58132211 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.797+283T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132211 | |||||||
| chr2:58132276 | C | T | 1 | a0002c0002t0002g0329 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.797+348C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132276 | |||||||
| chr2:58132348 | A | G | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.797+420A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132348 | |||||||
| chr2:58132406 | T | G | 1 | a0001c0003t0001g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.797+478T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132406 | |||||||
| chr2:58132545 | A | G | 26 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(23): Show |
26 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.797+617A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132545 | |||||||
| chr2:58132624 | A | G | 3 | a0001c0001t0002g0167 a0001c0001t0002g0208 a0001c0001t0006g0207 |
3 | HG02083.hp1 NA19056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.797+696A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132624 | |||||||
| chr2:58132695 | C | G | 18 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(15): Show |
18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.797+767C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132695 | |||||||
| chr2:58132724 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.797+796G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132724 | |||||||
| chr2:58132922 | A | G | 7 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(4): Show |
7 | HG01993.hp2 HG02004.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.797+994A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132922 | |||||||
| chr2:58132959 | T | G | 1 | a0001c0001t0001g0280 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.797+1031T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58132959 | |||||||
| chr2:58133131 | T | C | 21 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(18): Show |
21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.797+1203T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133131 | |||||||
| chr2:58133230 | T | TTATC | 39 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(36): Show |
39 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.797+1305_797+1306i others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 58133230 | ||||||
| chr2:58133247 | A | G | 19 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(16): Show |
19 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.797+1319A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133247 | |||||||
| chr2:58133269 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.797+1341A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133269 | |||||||
| chr2:58133474 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.797+1546G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133474 | |||||||
| chr2:58133487 | G | C | 5 | a0001c0001t0001g0119 a0001c0001t0001g0277 a0001c0001t0001g0278 others(2): Show |
5 | HG02145.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.797+1559G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133487 | |||||||
| chr2:58133510 | T | C | 16 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(13): Show |
16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.797+1582T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133510 | |||||||
| chr2:58133835 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.798-1306A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133835 | |||||||
| chr2:58133857 | C | T | 1 | a0002c0002t0002g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.798-1284C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133857 | |||||||
| chr2:58133976 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.798-1165C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133976 | |||||||
| chr2:58133999 | G | A | 89 | a0002c0002t0001g0025 a0002c0002t0001g0149 a0002c0002t0001g0150 others(86): Show |
90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.798-1142G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58133999 | |||||||
| chr2:58134013 | A | C | 1 | a0001c0001t0001g0309 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.798-1128A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134013 | |||||||
| chr2:58134041 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.798-1100T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134041 | |||||||
| chr2:58134088 | A | C | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.798-1053A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134088 | |||||||
| chr2:58134098 | T | A | 2 | a0002c0002t0001g0253 a0002c0002t0002g0254 |
2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.798-1043T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134098 | |||||||
| chr2:58134120 | T | C | 37 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(34): Show |
37 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.798-1021T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134120 | |||||||
| chr2:58134182 | G | A | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.798-959G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134182 | |||||||
| chr2:58134213 | A | C | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.798-928A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134213 | |||||||
| chr2:58134228 | T | C | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.798-913T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134228 | |||||||
| chr2:58134236 | G | A | 18 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.798-905G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134236 | |||||||
| chr2:58134291 | C | G | 1 | a0002c0002t0002g0112 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.798-850C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134291 | |||||||
| chr2:58134349 | C | T | 1 | a0002c0002t0002g0051 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.798-792C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134349 | |||||||
| chr2:58134378 | G | A | 21 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(18): Show |
21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.798-763G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134378 | |||||||
| chr2:58134385 | G | C | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.798-756G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134385 | |||||||
| chr2:58134410 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0327 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.798-731G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134410 | |||||||
| chr2:58134462 | T | C | 1 | a0001c0001t0002g0204 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.798-679T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134462 | |||||||
| chr2:58134540 | A | G | 1 | a0001c0001t0002g0184 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.798-601A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134540 | |||||||
| chr2:58134617 | C | CA | 77 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(74): Show |
79 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.798-504dupA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 58134617 | ||||||
| chr2:58134617 | C | CAA | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0019 others(52): Show |
58 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.798-505_798-504dup others(2): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 58134617 | ||||||
| chr2:58134617 | C | CAAA | 6 | a0001c0001t0001g0114 a0001c0001t0001g0119 a0001c0001t0001g0126 others(3): Show |
6 | HG01109.hp1 HG01952.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.798-506_798-504dup others(3): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 58134617 | ||||||
| chr2:58134617 | CA | C | 6 | a0001c0001t0001g0098 a0001c0001t0003g0245 a0001c0001t0003g0246 others(3): Show |
6 | HG01070.hp1 HG01256.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.798-504delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 58134617 | ||||||
| chr2:58134634 | A | T | 1 | a0001c0001t0002g0180 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.798-507A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134634 | |||||||
| chr2:58134768 | G | T | 7 | a0001c0001t0003g0241 a0001c0001t0003g0242 a0001c0001t0003g0243 others(4): Show |
7 | HG01256.hp1 HG01258.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.798-373G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134768 | |||||||
| chr2:58134809 | T | A | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.798-332T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134809 | |||||||
| chr2:58134884 | T | C | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.798-257T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58134884 | |||||||
| chr2:58135026 | G | A | 87 | a0002c0002t0001g0025 a0002c0002t0001g0253 a0002c0002t0002g0003 others(84): Show |
88 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.798-115G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 9/12 | chr2 | 58135026 | |||||||
| chr2:58135207 | A | G | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.856+8A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135207 | |||||||
| chr2:58135382 | G | C | 11 | a0002c0002t0002g0064 a0002c0002t0002g0066 a0002c0002t0002g0069 others(8): Show |
11 | HG00408.hp1 HG00558.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.856+183G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135382 | |||||||
| chr2:58135408 | A | G | 1 | a0002c0002t0002g0226 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.856+209A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135408 | |||||||
| chr2:58135441 | C | CT | 32 | a0001c0001t0001g0055 a0001c0001t0001g0101 a0001c0001t0001g0309 others(29): Show |
33 | HG01099.hp1 HG01106.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.856+258dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58135441 | ||||||
| chr2:58135441 | CT | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0138 a0001c0001t0001g0147 others(4): Show |
7 | HG01069.hp2 HG01070.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.856+258delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58135441 | ||||||
| chr2:58135473 | A | T | 1 | a0001c0001t0001g0316 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.856+274A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135473 | |||||||
| chr2:58135508 | G | T | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.856+309G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135508 | |||||||
| chr2:58135682 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.856+483T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135682 | |||||||
| chr2:58135823 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.856+624C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135823 | |||||||
| chr2:58135894 | C | T | 2 | a0001c0001t0001g0259 a0001c0001t0001g0327 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.856+695C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58135894 | |||||||
| chr2:58136181 | C | A | 1 | a0002c0002t0002g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.856+982C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136181 | |||||||
| chr2:58136214 | C | A | 1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.856+1015C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136214 | |||||||
| chr2:58136277 | GGA | G | 3 | a0001c0003t0001g0256 a0001c0003t0001g0257 a0001c0003t0001g0258 |
3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.856+1083_856+1084d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136277 | ||||||
| chr2:58136314 | A | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.856+1115A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136314 | |||||||
| chr2:58136388 | A | AT | 18 | a0001c0001t0002g0016 a0001c0003t0001g0009 a0001c0003t0001g0010 others(15): Show |
18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.856+1203dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136388 | ||||||
| chr2:58136388 | AT | A | 29 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(26): Show |
29 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.856+1203delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136388 | ||||||
| chr2:58136421 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.856+1222G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136421 | |||||||
| chr2:58136486 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.856+1287G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136486 | |||||||
| chr2:58136569 | G | C | 2 | a0001c0003t0001g0009 a0001c0003t0001g0010 |
2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.856+1370G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136569 | |||||||
| chr2:58136594 | A | C | 1 | a0001c0001t0001g0265 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.856+1395A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136594 | |||||||
| chr2:58136648 | G | T | 4 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(1): Show |
4 | HG03041.hp1 HG03453.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+1449G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136648 | |||||||
| chr2:58136763 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0101 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.856+1602_856+1622d others(23): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136763 | ||||||
| chr2:58136763 | ATATATAT others(14): Show |
A | 2 | a0001c0001t0001g0305 a0001c0001t0002g0005 |
3 | HG01168.hp1 HG01169.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.856+1602_856+1622d others(23): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136763 | ||||||
| chr2:58136794 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.856+1595C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136794 | |||||||
| chr2:58136830 | ATATATCA others(7): Show |
A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01167.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.856+1646_856+1659d others(16): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136830 | ||||||
| chr2:58136831 | T | G | 2 | a0002c0002t0002g0043 a0002c0002t0002g0070 |
2 | NA18945.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.856+1632T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136831 | |||||||
| chr2:58136839 | ATATAT | A | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+1646_856+1650d others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136839 | ||||||
| chr2:58136844 | TTA | T | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0164 |
3 | HG02280.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.856+1649_856+1650d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136844 | ||||||
| chr2:58136847 | TATC | T | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+1651_856+1653d others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136847 | ||||||
| chr2:58136857 | A | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01167.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.856+1658A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136857 | |||||||
| chr2:58136865 | ATATATCA others(5): Show |
A | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+1679_856+1690d others(14): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136865 | ||||||
| chr2:58136871 | C | CAT | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.856+1677_856+1678d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136871 | ||||||
| chr2:58136871 | C | CATATATA others(28): Show |
1 | a0001c0001t0001g0303 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.856+1678_856+1679i others(37): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136871 | ||||||
| chr2:58136878 | T | C | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+1679T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136878 | |||||||
| chr2:58136883 | C | A | 1 | a0002c0002t0002g0231 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.856+1684C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136883 | |||||||
| chr2:58136884 | A | T | 1 | a0002c0002t0002g0231 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.856+1685A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136884 | |||||||
| chr2:58136885 | T | C | 1 | a0002c0002t0002g0231 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.856+1686T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136885 | |||||||
| chr2:58136891 | TGTGTA | T | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+1693_856+1697d others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136891 | |||||||
| chr2:58136894 | G | A | 1 | a0002c0002t0002g0231 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.856+1695G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136894 | |||||||
| chr2:58136896 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0002g0213 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.856+1714_856+1741d others(30): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136896 | ||||||
| chr2:58136906 | TATATATA others(2): Show |
T | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+1714_856+1722d others(11): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136906 | ||||||
| chr2:58136907 | A | ATATAT | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(281): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.856+1709_856+1713d others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136907 | ||||||
| chr2:58136907 | A | ATATATTA others(33): Show |
7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+1713_856+1714i others(42): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136907 | ||||||
| chr2:58136907 | A | ATATTATA others(28): Show |
1 | a0002c0002t0002g0035 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.856+1711_856+1712i others(37): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136907 | ||||||
| chr2:58136909 | A | ATAT | 15 | a0001c0001t0001g0017 a0001c0001t0001g0142 a0001c0001t0001g0143 others(12): Show |
15 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.856+1711_856+1713d others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136909 | ||||||
| chr2:58136915 | C | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0142 a0001c0001t0001g0143 others(11): Show |
14 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+1716C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136915 | |||||||
| chr2:58136915 | C | CAT | 28 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(25): Show |
28 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.856+1721_856+1722d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136915 | ||||||
| chr2:58136916 | A | T | 14 | a0001c0001t0001g0017 a0001c0001t0001g0142 a0001c0001t0001g0143 others(11): Show |
14 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+1717A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136916 | |||||||
| chr2:58136917 | T | C | 14 | a0001c0001t0001g0017 a0001c0001t0001g0142 a0001c0001t0001g0143 others(11): Show |
14 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+1718T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136917 | |||||||
| chr2:58136917 | T | TATATATG others(28): Show |
1 | a0001c0001t0001g0326 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.856+1722_856+1723i others(37): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136917 | ||||||
| chr2:58136932 | C | A | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.856+1733C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136932 | |||||||
| chr2:58136933 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.856+1734A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136933 | |||||||
| chr2:58136934 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.856+1735T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136934 | |||||||
| chr2:58136940 | T | G | 1 | a0001c0001t0001g0176 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.856+1741T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136940 | |||||||
| chr2:58136965 | A | C | 1 | a0001c0001t0002g0213 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.856+1766A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136965 | |||||||
| chr2:58136966 | T | A | 1 | a0001c0001t0002g0213 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.856+1767T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136966 | |||||||
| chr2:58136967 | C | CAT | 14 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(11): Show |
14 | HG01884.hp1 HG01891.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.856+1773_856+1774d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58136967 | ||||||
| chr2:58136967 | C | T | 1 | a0001c0001t0002g0213 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.856+1768C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58136967 | |||||||
| chr2:58137007 | ATT | A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+1809_856+1810d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137007 | |||||||
| chr2:58137078 | A | T | 36 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(33): Show |
36 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.856+1879A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137078 | |||||||
| chr2:58137079 | CAT | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.856+1887_856+1888d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137079 | ||||||
| chr2:58137081 | T | TATATGTG others(26): Show |
3 | a0001c0001t0001g0056 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG02015.hp2 NA18747.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.856+1886_856+1887i others(35): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137081 | ||||||
| chr2:58137099 | A | T | 1 | a0002c0002t0002g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.856+1900A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137099 | |||||||
| chr2:58137156 | T | TTATATAT others(22): Show |
2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01167.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.856+1973_856+1974i others(31): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137156 | ||||||
| chr2:58137156 | TTA | T | 7 | a0001c0001t0001g0056 a0001c0003t0001g0261 a0001c0003t0001g0263 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.856+1965_856+1966d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137156 | ||||||
| chr2:58137158 | A | G | 3 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0006c0010t0001g0148 |
3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.856+1959A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137158 | |||||||
| chr2:58137165 | T | TCATATAT others(4): Show |
1 | a0002c0002t0002g0273 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.856+1973_856+1974i others(13): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137165 | ||||||
| chr2:58137166 | C | CAT | 4 | a0001c0001t0001g0142 a0001c0001t0001g0147 a0001c0003t0001g0268 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+1972_856+1973d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137166 | ||||||
| chr2:58137172 | T | TATCATAT others(121): Show |
1 | a0001c0001t0001g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.856+1973_856+1974i others(130): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137172 | |||||||
| chr2:58137172 | T | TATCATAT others(99): Show |
2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.856+1973_856+1974i others(108): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137172 | |||||||
| chr2:58137172 | T | TATCATAT others(119): Show |
4 | a0001c0001t0001g0017 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
4 | HG02280.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+1973_856+1974i others(128): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137172 | |||||||
| chr2:58137172 | T | TATCATAT others(119): Show |
3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02647.hp2 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.856+1973_856+1974i others(128): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137172 | |||||||
| chr2:58137172 | T | TATCATAT others(119): Show |
1 | a0001c0001t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.856+1973_856+1974i others(128): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137172 | |||||||
| chr2:58137172 | T | TCATATAT others(176): Show |
3 | a0001c0001t0001g0114 a0001c0001t0001g0123 a0007c0009t0001g0124 |
3 | HG03195.hp1 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(185): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137172 | ||||||
| chr2:58137172 | T | TCATATAT others(196): Show |
3 | a0001c0001t0001g0121 a0003c0005t0001g0116 a0003c0005t0001g0117 |
3 | HG02109.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(205): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137172 | ||||||
| chr2:58137172 | T | TCATATAT others(216): Show |
4 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0122 others(1): Show |
4 | HG01109.hp2 HG01243.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(225): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137172 | ||||||
| chr2:58137172 | T | TCATATAT others(236): Show |
1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(245): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137172 | ||||||
| chr2:58137172 | T | TCATATAT others(198): Show |
1 | a0001c0001t0001g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(207): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137172 | ||||||
| chr2:58137172 | T | TCATATAT others(194): Show |
1 | a0001c0001t0001g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(203): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137172 | ||||||
| chr2:58137178 | A | ATATCATA others(144): Show |
1 | a0002c0002t0002g0227 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(153): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137178 | ||||||
| chr2:58137180 | A | ATC | 11 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp2 HG02559.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.856+1982_856+1983d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(180): Show |
1 | a0001c0001t0001g0127 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(189): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(134): Show |
1 | a0001c0001t0001g0260 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(143): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(234): Show |
1 | a0001c0004t0001g0131 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(243): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(212): Show |
1 | a0001c0004t0001g0132 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(221): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(168): Show |
1 | a0001c0001t0001g0306 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(163): Show |
1 | a0001c0001t0001g0125 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(172): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(185): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(10): Show |
16 | HG00099.hp1 HG01109.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(194): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(207): Show |
1 | a0001c0001t0001g0140 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(216): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(141): Show |
6 | a0001c0001t0001g0287 a0001c0001t0001g0295 a0001c0001t0001g0299 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(150): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(163): Show |
1 | a0001c0001t0001g0293 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(172): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(185): Show |
1 | a0001c0001t0001g0255 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(194): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(141): Show |
6 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0300 others(3): Show |
6 | HG00438.hp1 HG01975.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(150): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(163): Show |
8 | a0001c0001t0001g0119 a0001c0001t0001g0277 a0001c0001t0001g0278 others(5): Show |
8 | HG00323.hp2 HG00597.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(172): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(115): Show |
2 | a0001c0001t0001g0142 a0001c0001t0001g0147 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(124): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(203): Show |
2 | a0001c0001t0001g0052 a0001c0001t0001g0274 |
2 | HG02886.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(212): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(181): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(7): Show |
12 | HG01928.hp2 NA18945.hp1 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(190): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(159): Show |
2 | a0001c0001t0001g0050 a0001c0001t0001g0280 |
2 | HG03654.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(168): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(181): Show |
4 | a0001c0001t0001g0176 a0001c0001t0001g0216 a0001c0001t0001g0235 others(1): Show |
4 | NA18964.hp2 NA18977.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(190): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(181): Show |
1 | a0001c0001t0001g0088 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(190): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(195): Show |
1 | a0001c0001t0001g0276 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(204): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(289): Show |
1 | a0001c0001t0001g0283 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(298): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(139): Show |
4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(148): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(179): Show |
1 | a0001c0001t0001g0178 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(188): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(170): Show |
2 | a0001c0001t0001g0262 a0001c0001t0001g0264 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(179): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(212): Show |
1 | a0001c0001t0001g0175 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(221): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(256): Show |
1 | a0001c0001t0001g0179 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(265): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(168): Show |
15 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0053 others(12): Show |
15 | HG00423.hp2 HG00735.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(190): Show |
4 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG04199.hp1 NA18971.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(190): Show |
2 | a0001c0001t0001g0055 a0001c0001t0001g0290 |
2 | HG01496.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(146): Show |
2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG01243.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(140): Show |
2 | a0002c0002t0001g0149 a0002c0002t0001g0150 |
2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(149): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(162): Show |
1 | a0006c0010t0001g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(171): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(227): Show |
2 | a0001c0001t0001g0136 a0001c0001t0001g0138 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(236): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(173): Show |
1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.856+2002_856+2003i others(182): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(195): Show |
1 | a0001c0001t0001g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.856+2002_856+2003i others(204): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(92): Show |
1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.856+2002_856+2003i others(101): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(114): Show |
1 | a0001c0001t0001g0163 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.856+2002_856+2003i others(123): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(190): Show |
1 | a0001c0001t0002g0202 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(168): Show |
5 | a0001c0001t0002g0007 a0001c0001t0002g0169 a0001c0001t0002g0171 others(2): Show |
6 | NA18955.hp1 NA18969.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(190): Show |
1 | a0001c0001t0002g0197 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(146): Show |
1 | a0001c0001t0002g0018 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(222): Show |
1 | a0002c0002t0002g0078 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(231): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(217): Show |
4 | a0001c0001t0002g0177 a0001c0001t0002g0193 a0001c0001t0002g0194 others(1): Show |
4 | HG00741.hp1 HG01433.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(226): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(217): Show |
1 | a0001c0001t0002g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(226): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(173): Show |
2 | a0001c0001t0001g0249 a0001c0001t0001g0252 |
2 | HG02615.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(182): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(170): Show |
1 | a0001c0001t0002g0191 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(179): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(146): Show |
1 | a0001c0001t0002g0190 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(190): Show |
4 | a0001c0001t0002g0167 a0001c0001t0002g0237 a0001c0001t0002g0238 others(1): Show |
4 | HG02165.hp1 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(212): Show |
2 | a0001c0001t0003g0242 a0001c0001t0003g0243 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(221): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(234): Show |
1 | a0001c0001t0003g0246 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(243): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(168): Show |
26 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0040 others(23): Show |
28 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(190): Show |
10 | a0001c0001t0002g0172 a0001c0001t0002g0180 a0001c0001t0002g0212 others(7): Show |
10 | HG00280.hp2 HG00735.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(212): Show |
3 | a0001c0001t0002g0182 a0001c0001t0002g0211 a0001c0001t0003g0241 |
3 | HG02145.hp2 HG02698.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(221): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(166): Show |
1 | a0001c0001t0002g0210 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(175): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(146): Show |
1 | a0001c0001t0002g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(190): Show |
1 | a0002c0002t0002g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(190): Show |
2 | a0002c0002t0002g0021 a0002c0002t0002g0075 |
2 | HG01074.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(190): Show |
1 | a0002c0002t0002g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(206): Show |
1 | a0001c0001t0002g0217 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(215): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(168): Show |
1 | a0001c0001t0002g0222 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(188): Show |
1 | a0001c0001t0002g0204 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(197): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(168): Show |
2 | a0001c0001t0002g0005 a0001c0001t0002g0165 |
3 | HG01168.hp1 HG01169.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(190): Show |
1 | a0001c0001t0002g0251 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(141): Show |
1 | a0001c0001t0002g0206 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(150): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137180 | A | ATCATATA others(185): Show |
1 | a0001c0001t0002g0170 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(194): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137180 | ||||||
| chr2:58137182 | C | CATATATA others(416): Show |
1 | a0001c0001t0001g0327 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(425): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(370): Show |
1 | a0001c0001t0001g0259 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(379): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(302): Show |
1 | a0001c0001t0001g0323 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(311): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(324): Show |
1 | a0001c0001t0001g0319 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(333): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(324): Show |
1 | a0001c0001t0001g0320 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(333): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(280): Show |
1 | a0001c0001t0001g0321 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(289): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(262): Show |
3 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(271): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(278): Show |
2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.856+1989_856+1990i others(287): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(278): Show |
1 | a0001c0001t0001g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(287): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(412): Show |
1 | a0001c0001t0001g0317 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(421): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(390): Show |
1 | a0001c0001t0001g0316 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(399): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(390): Show |
1 | a0001c0001t0001g0315 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(399): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(250): Show |
1 | a0001c0001t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(259): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(254): Show |
1 | a0001c0001t0001g0310 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(263): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(254): Show |
1 | a0001c0001t0001g0309 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(263): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(346): Show |
1 | a0001c0003t0001g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(355): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(456): Show |
1 | a0001c0003t0001g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.856+1989_856+1990i others(465): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATA others(386): Show |
1 | a0001c0003t0001g0256 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.856+1989_856+1990i others(395): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(175): Show |
1 | a0002c0002t0002g0064 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(184): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(67): Show |
1 | a0002c0002t0002g0033 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(76): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(247): Show |
1 | a0002c0002t0002g0044 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(256): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(200): Show |
4 | a0002c0002t0002g0043 a0002c0002t0002g0070 a0002c0002t0002g0076 others(1): Show |
4 | HG01975.hp2 HG02293.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(209): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(200): Show |
1 | a0002c0002t0002g0071 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(209): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(177): Show |
1 | a0002c0002t0002g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(186): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(199): Show |
1 | a0002c0002t0001g0025 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(208): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(129): Show |
1 | a0002c0002t0002g0100 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(138): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(173): Show |
10 | a0002c0002t0002g0003 a0002c0002t0002g0046 a0002c0002t0002g0059 others(7): Show |
11 | HG00323.hp1 HG00621.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(182): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(200): Show |
1 | a0002c0002t0002g0108 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(209): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(166): Show |
2 | a0002c0002t0002g0079 a0002c0002t0002g0080 |
2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(175): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(188): Show |
1 | a0002c0002t0001g0253 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(197): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(122): Show |
1 | a0002c0002t0002g0024 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(131): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(80): Show |
1 | a0002c0002t0002g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(89): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(102): Show |
2 | a0002c0002t0002g0083 a0002c0002t0002g0102 |
2 | HG01496.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(111): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(146): Show |
27 | a0001c0001t0002g0016 a0002c0002t0002g0028 a0002c0002t0002g0029 others(24): Show |
27 | HG00408.hp1 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(168): Show |
4 | a0002c0002t0002g0091 a0002c0002t0002g0107 a0002c0002t0002g0156 others(1): Show |
4 | HG00558.hp2 HG00621.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(190): Show |
1 | a0002c0002t0005g0109 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(199): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(234): Show |
1 | a0002c0002t0002g0084 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(243): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(146): Show |
1 | a0002c0002t0002g0066 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(168): Show |
1 | a0002c0002t0002g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(177): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(104): Show |
1 | a0002c0002t0002g0112 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(113): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(173): Show |
2 | a0002c0002t0002g0226 a0008c0008t0002g0232 |
2 | NA18977.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(182): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(80): Show |
1 | a0002c0002t0002g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(89): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(146): Show |
5 | a0002c0002t0002g0228 a0002c0002t0002g0229 a0002c0002t0002g0230 others(2): Show |
5 | HG02027.hp1 HG02040.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.856+2000_856+2001i others(155): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(186): Show |
1 | a0002c0002t0002g0329 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(195): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | C | CATATATG others(119): Show |
1 | a0002c0002t0002g0051 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(128): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137182 | CATATATG others(6): Show |
C | 6 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+1990_856+2002d others(15): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137182 | ||||||
| chr2:58137184 | T | TATATGAT others(208): Show |
1 | a0001c0001t0002g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(217): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137184 | ||||||
| chr2:58137188 | T | TATCATAT others(62): Show |
7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+1989_856+1990i others(71): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137188 | |||||||
| chr2:58137193 | C | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.856+1994C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137193 | |||||||
| chr2:58137193 | CAT | C | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+2001_856+2002d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137193 | ||||||
| chr2:58137195 | T | TATATCAT others(171): Show |
2 | a0002c0002t0002g0041 a0002c0002t0002g0042 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.856+2000_856+2001i others(180): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137195 | ||||||
| chr2:58137195 | T | TATATCAT others(193): Show |
1 | a0002c0002t0002g0082 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(202): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137195 | ||||||
| chr2:58137195 | T | TGTATCAT others(11): Show |
2 | a0001c0003t0001g0268 a0001c0003t0001g0269 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.856+1996_856+1997i others(20): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137195 | |||||||
| chr2:58137198 | A | ATCATATA others(217): Show |
1 | a0002c0002t0002g0095 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.856+2000_856+2001i others(226): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137198 | ||||||
| chr2:58137198 | A | ATCATATA others(188): Show |
1 | a0002c0002t0002g0254 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(197): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137198 | ||||||
| chr2:58137198 | A | ATCATATA others(102): Show |
1 | a0002c0002t0002g0062 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(111): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137198 | ||||||
| chr2:58137198 | A | ATCATATA others(183): Show |
1 | a0002c0002t0002g0273 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.856+2000_856+2001i others(192): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137198 | ||||||
| chr2:58137198 | A | G | 9 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(6): Show |
9 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.856+1999A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137198 | |||||||
| chr2:58137200 | ATC | A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.856+2004_856+2005d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137200 | ||||||
| chr2:58137202 | C | A | 19 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0002g0286 others(16): Show |
19 | HG00323.hp2 HG00597.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.856+2003C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137202 | |||||||
| chr2:58137203 | T | A | 32 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(29): Show |
32 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.856+2004T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137203 | |||||||
| chr2:58137204 | C | T | 32 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(29): Show |
32 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.856+2005C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137204 | |||||||
| chr2:58137218 | A | G | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+2019A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137218 | |||||||
| chr2:58137220 | A | G | 3 | a0002c0002t0002g0062 a0002c0002t0002g0074 a0002c0002t0002g0112 |
3 | HG01255.hp2 HG01361.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.856+2021A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137220 | |||||||
| chr2:58137221 | T | TC | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+2022_856+2023i others(3): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137221 | |||||||
| chr2:58137222 | A | C | 1 | a0001c0001t0002g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.856+2023A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137222 | |||||||
| chr2:58137223 | T | TA | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.856+2024_856+2025i others(3): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137223 | |||||||
| chr2:58137224 | C | CAT | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.856+2028_856+2029d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137224 | ||||||
| chr2:58137224 | C | CATAT | 21 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(18): Show |
21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.856+2026_856+2029d others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137224 | ||||||
| chr2:58137224 | C | CATATGAT others(13): Show |
1 | a0001c0001t0001g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.856+2030_856+2049d others(22): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137224 | ||||||
| chr2:58137224 | C | CTCAT | 5 | a0001c0001t0002g0208 a0002c0002t0002g0044 a0002c0002t0002g0062 others(2): Show |
5 | HG01433.hp2 HG02165.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.856+2025_856+2026i others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137224 | |||||||
| chr2:58137224 | C | CTCATATA others(17): Show |
1 | a0002c0002t0002g0273 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.856+2025_856+2026i others(26): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137224 | |||||||
| chr2:58137224 | C | T | 9 | a0001c0001t0001g0031 a0001c0003t0001g0261 a0001c0003t0001g0263 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.856+2025C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137224 | |||||||
| chr2:58137224 | CAT | C | 4 | a0001c0001t0002g0177 a0001c0001t0002g0193 a0001c0001t0002g0194 others(1): Show |
4 | HG00741.hp1 HG01433.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+2028_856+2029d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137224 | ||||||
| chr2:58137233 | CAT | C | 6 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+2041_856+2042d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137233 | ||||||
| chr2:58137238 | A | G | 6 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+2039A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137238 | |||||||
| chr2:58137242 | C | CATATATG others(62): Show |
1 | a0001c0001t0001g0260 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.856+2049_856+2050i others(71): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137242 | ||||||
| chr2:58137242 | CATATATA others(11): Show |
C | 2 | a0001c0003t0001g0268 a0001c0003t0001g0269 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.856+2053_856+2070d others(20): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137242 | ||||||
| chr2:58137251 | G | GATAC | 13 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(10): Show |
13 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.856+2055_856+2056i others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 58137251 | ||||||
| chr2:58137255 | T | C | 22 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(19): Show |
22 | HG01891.hp2 HG02071.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.856+2056T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137255 | |||||||
| chr2:58137260 | G | C | 6 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+2061G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137260 | |||||||
| chr2:58137318 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.856+2119G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137318 | |||||||
| chr2:58137495 | A | G | 1 | a0002c0002t0002g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.857-2171A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137495 | |||||||
| chr2:58137530 | A | G | 3 | a0001c0003t0001g0267 a0001c0003t0001g0270 a0001c0003t0001g0272 |
3 | HG01884.hp2 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.857-2136A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137530 | |||||||
| chr2:58137607 | T | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(66): Show |
74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.857-2059T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137607 | |||||||
| chr2:58137618 | G | A | 1 | a0002c0002t0002g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.857-2048G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137618 | |||||||
| chr2:58137691 | C | G | 1 | a0001c0001t0002g0200 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.857-1975C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137691 | |||||||
| chr2:58137803 | T | G | 1 | a0001c0001t0001g0262 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.857-1863T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137803 | |||||||
| chr2:58137915 | T | A | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1751T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137915 | |||||||
| chr2:58137916 | A | C | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1750A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137916 | |||||||
| chr2:58137917 | C | A | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1749C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137917 | |||||||
| chr2:58137919 | C | T | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1747C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137919 | |||||||
| chr2:58137920 | T | A | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1746T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137920 | |||||||
| chr2:58137922 | C | T | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1744C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137922 | |||||||
| chr2:58137923 | A | G | 9 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0118 others(6): Show |
9 | HG01109.hp2 HG01243.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.857-1743A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137923 | |||||||
| chr2:58137924 | G | C | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1742G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137924 | |||||||
| chr2:58137925 | G | A | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1741G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137925 | |||||||
| chr2:58137927 | T | A | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857-1739T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58137927 | |||||||
| chr2:58138015 | C | G | 1 | a0001c0001t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.857-1651C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138015 | |||||||
| chr2:58138215 | A | C | 21 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(18): Show |
21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.857-1451A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138215 | |||||||
| chr2:58138408 | C | T | 1 | a0002c0002t0002g0034 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.857-1258C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138408 | |||||||
| chr2:58138444 | A | G | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.857-1222A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138444 | |||||||
| chr2:58138540 | G | T | 1 | a0001c0001t0001g0303 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.857-1126G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138540 | |||||||
| chr2:58138574 | C | T | 1 | a0002c0002t0002g0024 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.857-1092C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138574 | |||||||
| chr2:58138760 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.857-906T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138760 | |||||||
| chr2:58138841 | A | G | 1 | a0002c0002t0002g0046 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.857-825A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138841 | |||||||
| chr2:58138906 | T | C | 1 | a0002c0002t0002g0035 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.857-760T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138906 | |||||||
| chr2:58138987 | A | C | 1 | a0001c0001t0001g0265 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.857-679A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58138987 | |||||||
| chr2:58139373 | A | C | 1 | a0002c0002t0002g0073 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.857-293A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58139373 | |||||||
| chr2:58139384 | T | G | 2 | a0001c0001t0003g0242 a0001c0001t0003g0243 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.857-282T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58139384 | |||||||
| chr2:58139468 | A | T | 1 | a0001c0001t0003g0241 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.857-198A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58139468 | |||||||
| chr2:58139543 | T | C | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.857-123T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 10/12 | chr2 | 58139543 | |||||||
| chr2:58139957 | T | C | 36 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(33): Show |
36 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1023+125T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58139957 | |||||||
| chr2:58140003 | G | A | 3 | a0001c0003t0001g0256 a0001c0003t0001g0257 a0001c0003t0001g0258 |
3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1023+171G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140003 | |||||||
| chr2:58140060 | G | A | 1 | a0002c0002t0002g0075 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1023+228G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140060 | |||||||
| chr2:58140269 | TACA | T | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1023+438_1023+440d others(5): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140269 | |||||||
| chr2:58140273 | G | C | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1023+441G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140273 | |||||||
| chr2:58140360 | C | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1023+528C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140360 | |||||||
| chr2:58140917 | C | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0250 |
2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1023+1085C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140917 | |||||||
| chr2:58140986 | C | T | 2 | a0001c0003t0001g0257 a0001c0003t0001g0258 |
2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1023+1154C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58140986 | |||||||
| chr2:58141071 | TTTAATAA others(6): Show |
T | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1023+1240_1023+125 others(17): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141071 | |||||||
| chr2:58141275 | A | T | 1 | a0001c0001t0001g0265 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1023+1443A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141275 | |||||||
| chr2:58141520 | G | A | 2 | a0001c0003t0001g0009 a0001c0003t0001g0010 |
2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1023+1688G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141520 | |||||||
| chr2:58141684 | T | C | 8 | a0001c0003t0001g0261 a0001c0003t0001g0263 a0001c0003t0001g0267 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+1852T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141684 | |||||||
| chr2:58141703 | T | G | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1023+1871T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141703 | |||||||
| chr2:58141740 | T | G | 2 | a0001c0001t0002g0238 a0001c0001t0002g0239 |
2 | NA18992.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1023+1908T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141740 | |||||||
| chr2:58141832 | C | T | 1 | a0001c0003t0001g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1023+2000C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141832 | |||||||
| chr2:58141849 | A | T | 1 | a0001c0001t0001g0276 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1023+2017A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58141849 | |||||||
| chr2:58142108 | C | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA19001.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1023+2276C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58142108 | |||||||
| chr2:58142170 | A | T | 1 | a0002c0002t0002g0110 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1023+2338A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58142170 | |||||||
| chr2:58142197 | A | C | 1 | a0001c0001t0001g0304 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1023+2365A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58142197 | |||||||
| chr2:58142324 | G | GT | 21 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(18): Show |
21 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1023+2506dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 58142324 | ||||||
| chr2:58142920 | C | T | 1 | a0001c0001t0002g0195 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1023+3088C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58142920 | |||||||
| chr2:58143077 | A | G | 3 | a0001c0003t0001g0256 a0001c0003t0001g0257 a0001c0003t0001g0258 |
3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1024-3239A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143077 | |||||||
| chr2:58143207 | T | G | 2 | a0001c0001t0002g0182 a0001c0001t0002g0225 |
2 | HG02027.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1024-3109T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143207 | |||||||
| chr2:58143312 | A | G | 21 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(18): Show |
21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1024-3004A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143312 | |||||||
| chr2:58143403 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1024-2913G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143403 | |||||||
| chr2:58143412 | A | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1024-2904A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143412 | |||||||
| chr2:58143481 | T | C | 21 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(18): Show |
21 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1024-2835T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143481 | |||||||
| chr2:58143588 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1024-2728T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143588 | |||||||
| chr2:58143614 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1024-2702G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143614 | |||||||
| chr2:58143630 | G | C | 25 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(22): Show |
25 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.1024-2686G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143630 | |||||||
| chr2:58143945 | T | C | 9 | a0001c0001t0001g0142 a0001c0003t0001g0261 a0001c0003t0001g0263 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1024-2371T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143945 | |||||||
| chr2:58143968 | T | C | 2 | a0001c0001t0002g0196 a0001c0001t0002g0206 |
2 | HG00408.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1024-2348T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58143968 | |||||||
| chr2:58144010 | T | C | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-2306T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144010 | |||||||
| chr2:58144012 | T | C | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-2304T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144012 | |||||||
| chr2:58144018 | T | C | 89 | a0001c0001t0002g0016 a0002c0002t0001g0149 a0002c0002t0001g0150 others(86): Show |
90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1024-2298T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144018 | |||||||
| chr2:58144034 | T | C | 11 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1024-2282T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144034 | |||||||
| chr2:58144222 | C | T | 21 | a0001c0001t0001g0274 a0001c0001t0001g0284 a0001c0001t0001g0285 others(18): Show |
21 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.1024-2094C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144222 | |||||||
| chr2:58144233 | G | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(4): Show |
7 | HG01109.hp2 HG01243.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1024-2083G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144233 | |||||||
| chr2:58144275 | T | C | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1024-2041T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144275 | |||||||
| chr2:58144331 | G | A | 1 | a0001c0001t0001g0284 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1024-1985G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144331 | |||||||
| chr2:58144921 | C | A | 2 | a0001c0001t0002g0233 a0001c0001t0002g0234 |
2 | NA18991.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1024-1395C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58144921 | |||||||
| chr2:58145008 | T | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | NA19001.hp1 NA19057.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-1308T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145008 | |||||||
| chr2:58145016 | T | C | 16 | a0001c0001t0001g0142 a0001c0003t0001g0009 a0001c0003t0001g0010 others(13): Show |
16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1024-1300T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145016 | |||||||
| chr2:58145040 | C | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1024-1276C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145040 | |||||||
| chr2:58145214 | G | A | 2 | a0001c0003t0001g0009 a0001c0003t0001g0010 |
2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1024-1102G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145214 | |||||||
| chr2:58145319 | C | T | 20 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(17): Show |
20 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.1024-997C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145319 | |||||||
| chr2:58145321 | A | G | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-995A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145321 | |||||||
| chr2:58145348 | C | T | 3 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0006c0010t0001g0148 |
3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1024-968C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145348 | |||||||
| chr2:58145368 | CA | C | 17 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0031 others(14): Show |
17 | HG01928.hp2 HG01934.hp2 HG03654.hp2 others(14): Show |
intron_variant | MODIFIER | c.1024-943delA | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 58145368 | ||||||
| chr2:58145455 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1024-861A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145455 | |||||||
| chr2:58145459 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(61): Show |
66 | HG00423.hp2 HG00735.hp1 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.1024-857G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145459 | |||||||
| chr2:58145540 | A | G | 1 | a0002c0002t0002g0330 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1024-776A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145540 | |||||||
| chr2:58145542 | T | A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1024-774T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145542 | |||||||
| chr2:58145553 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1024-763A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145553 | |||||||
| chr2:58145626 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1024-690A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145626 | |||||||
| chr2:58145681 | TTATTACA | T | 6 | a0001c0001t0001g0175 a0001c0001t0001g0179 a0001c0001t0001g0262 others(3): Show |
6 | HG00738.hp1 HG01243.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-631_1024-625d others(9): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 58145681 | ||||||
| chr2:58145779 | C | T | 6 | a0001c0001t0001g0175 a0001c0001t0001g0179 a0001c0001t0001g0262 others(3): Show |
6 | HG00738.hp1 HG01243.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-537C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145779 | |||||||
| chr2:58145781 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1024-535C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145781 | |||||||
| chr2:58145843 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(46): Show |
52 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.1024-473A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58145843 | |||||||
| chr2:58146018 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1024-298A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146018 | |||||||
| chr2:58146050 | C | G | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1024-266C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146050 | |||||||
| chr2:58146070 | C | T | 76 | a0001c0001t0002g0016 a0002c0002t0001g0253 a0002c0002t0002g0003 others(73): Show |
77 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1024-246C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146070 | |||||||
| chr2:58146146 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1024-170T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146146 | |||||||
| chr2:58146156 | G | A | 9 | a0001c0001t0001g0142 a0001c0003t0001g0261 a0001c0003t0001g0263 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1024-160G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146156 | |||||||
| chr2:58146165 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1024-151T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146165 | |||||||
| chr2:58146312 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18977.hp2 | splice_region_variant&intron_variant | LOW | c.1024-4A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 11/12 | chr2 | 58146312 | |||||||
| chr2:58146489 | T | C | 1 | a0002c0002t0002g0024 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1182+15T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58146489 | |||||||
| chr2:58146619 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1182+145G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58146619 | |||||||
| chr2:58146631 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1182+157A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58146631 | |||||||
| chr2:58146637 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1182+163G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58146637 | |||||||
| chr2:58146733 | T | A | 1 | a0001c0001t0001g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1182+259T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58146733 | |||||||
| chr2:58146767 | ATG | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(36): Show |
41 | HG00423.hp2 HG00735.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.1182+295_1182+296d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58146767 | ||||||
| chr2:58146769 | GTA | G | 3 | a0001c0001t0001g0105 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG02015.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1182+297_1182+298d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58146769 | ||||||
| chr2:58146801 | C | G | 5 | a0001c0001t0001g0142 a0001c0003t0001g0267 a0001c0003t0001g0270 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182+327C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58146801 | |||||||
| chr2:58147121 | C | G | 1 | a0001c0001t0002g0203 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1182+647C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147121 | |||||||
| chr2:58147258 | A | G | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+784A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147258 | |||||||
| chr2:58147563 | G | A | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+1089G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147563 | |||||||
| chr2:58147610 | A | G | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+1136A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147610 | |||||||
| chr2:58147658 | TTTCCC | T | 6 | a0001c0001t0001g0175 a0001c0001t0001g0179 a0001c0001t0001g0262 others(3): Show |
6 | HG00738.hp1 HG01243.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182+1186_1182+119 others(9): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58147658 | ||||||
| chr2:58147664 | T | A | 6 | a0001c0001t0001g0175 a0001c0001t0001g0179 a0001c0001t0001g0262 others(3): Show |
6 | HG00738.hp1 HG01243.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182+1190T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147664 | |||||||
| chr2:58147797 | A | T | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG01167.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182+1323A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147797 | |||||||
| chr2:58147800 | G | GT | 8 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0128 others(5): Show |
8 | HG01070.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1182+1342dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58147800 | ||||||
| chr2:58147800 | GT | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0023 others(172): Show |
178 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.1182+1342delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58147800 | ||||||
| chr2:58147877 | T | G | 7 | a0001c0001t0001g0142 a0001c0003t0001g0267 a0001c0003t0001g0268 others(4): Show |
7 | HG01884.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1182+1403T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147877 | |||||||
| chr2:58147896 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1182+1422A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58147896 | |||||||
| chr2:58148120 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1182+1646T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148120 | |||||||
| chr2:58148187 | A | G | 11 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1182+1713A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148187 | |||||||
| chr2:58148221 | T | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(314): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1182+1747T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148221 | |||||||
| chr2:58148251 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1182+1777G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148251 | |||||||
| chr2:58148258 | A | G | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+1784A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148258 | |||||||
| chr2:58148427 | T | A | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
5 | HG02258.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182+1953T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148427 | |||||||
| chr2:58148553 | C | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(77): Show |
82 | HG00423.hp2 HG00735.hp1 HG01261.hp2 others(79): Show |
intron_variant | MODIFIER | c.1182+2079C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148553 | |||||||
| chr2:58148716 | G | C | 1 | a0001c0001t0002g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1182+2242G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148716 | |||||||
| chr2:58148839 | A | G | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+2365A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148839 | |||||||
| chr2:58148850 | T | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1182+2376T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148850 | |||||||
| chr2:58148899 | G | A | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+2425G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58148899 | |||||||
| chr2:58149178 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0255 |
2 | HG01109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1182+2704C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149178 | |||||||
| chr2:58149452 | G | C | 1 | a0002c0002t0002g0082 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1182+2978G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149452 | |||||||
| chr2:58149456 | T | C | 6 | a0001c0001t0001g0175 a0001c0001t0001g0179 a0001c0001t0001g0262 others(3): Show |
6 | HG00738.hp1 HG01243.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182+2982T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149456 | |||||||
| chr2:58149746 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1182+3272A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149746 | |||||||
| chr2:58149871 | A | G | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+3397A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149871 | |||||||
| chr2:58149879 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1182+3405T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149879 | |||||||
| chr2:58149888 | A | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1182+3414A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58149888 | |||||||
| chr2:58149991 | CTTTTCTT others(5): Show |
C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0275 |
4 | NA18945.hp1 NA18952.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+3522_1182+353 others(16): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58149991 | ||||||
| chr2:58149996 | CT | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(218): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1182+3540delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58149996 | ||||||
| chr2:58149996 | CTTT | C | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+3538_1182+354 others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58149996 | ||||||
| chr2:58150097 | G | A | 1 | a0002c0002t0002g0226 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1182+3623G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150097 | |||||||
| chr2:58150156 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1182+3682T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150156 | |||||||
| chr2:58150206 | G | A | 6 | a0001c0001t0001g0049 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02258.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182+3732G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150206 | |||||||
| chr2:58150308 | A | AT | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+3842dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58150308 | ||||||
| chr2:58150561 | A | G | 2 | a0001c0003t0001g0261 a0001c0003t0001g0263 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1182+4087A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150561 | |||||||
| chr2:58150561 | A | T | 3 | a0001c0003t0001g0256 a0001c0003t0001g0257 a0001c0003t0001g0258 |
3 | HG02572.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1182+4087A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150561 | |||||||
| chr2:58150562 | GT | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
137 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(134): Show |
intron_variant | MODIFIER | c.1182+4102delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58150562 | ||||||
| chr2:58150563 | T | TTTTTTTT others(6): Show |
2 | a0001c0003t0001g0261 a0001c0003t0001g0263 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1182+4100_1182+410 others(17): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58150563 | ||||||
| chr2:58150565 | T | G | 1 | a0001c0003t0001g0256 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1182+4091T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150565 | |||||||
| chr2:58150756 | G | A | 114 | a0001c0001t0001g0119 a0001c0001t0001g0274 a0001c0001t0001g0277 others(111): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1182+4282G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150756 | |||||||
| chr2:58150942 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1182+4468C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58150942 | |||||||
| chr2:58150942 | CTTT | C | 9 | a0001c0001t0001g0142 a0001c0003t0001g0261 a0001c0003t0001g0263 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1182+4472_1182+447 others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58150942 | ||||||
| chr2:58151006 | T | G | 1 | a0001c0001t0001g0056 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1182+4532T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151006 | |||||||
| chr2:58151080 | A | C | 9 | a0001c0001t0001g0142 a0001c0003t0001g0261 a0001c0003t0001g0263 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1182+4606A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151080 | |||||||
| chr2:58151251 | A | G | 3 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0006c0010t0001g0148 |
3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1182+4777A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151251 | |||||||
| chr2:58151502 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1182+5028G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151502 | |||||||
| chr2:58151526 | A | C | 3 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0006c0010t0001g0148 |
3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1182+5052A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151526 | |||||||
| chr2:58151572 | TCCATTTC others(38): Show |
T | 1 | a0002c0002t0002g0230 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1182+5104_1182+514 others(49): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151572 | ||||||
| chr2:58151731 | G | GT | 34 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0058 others(31): Show |
35 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.1182+5293dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTT | 30 | a0001c0001t0001g0002 a0001c0001t0001g0115 a0001c0001t0001g0120 others(27): Show |
32 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1182+5292_1182+529 others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTT | 12 | a0001c0001t0001g0259 a0001c0001t0001g0312 a0001c0001t0001g0313 others(9): Show |
12 | HG00741.hp1 HG01433.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1182+5291_1182+529 others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTT | 6 | a0001c0001t0001g0248 a0001c0001t0001g0321 a0001c0001t0001g0324 others(3): Show |
6 | HG02723.hp2 HG02922.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1182+5290_1182+529 others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT | 11 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0101 others(8): Show |
11 | HG00558.hp2 HG01261.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1182+5287_1182+529 others(11): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(1): Show |
14 | a0001c0001t0001g0087 a0001c0001t0001g0094 a0001c0001t0001g0176 others(11): Show |
14 | HG01255.hp2 HG01433.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1182+5286_1182+529 others(12): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(2): Show |
19 | a0001c0001t0001g0032 a0001c0001t0001g0289 a0001c0003t0001g0257 others(16): Show |
20 | HG00621.hp1 HG00621.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1182+5285_1182+529 others(13): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(3): Show |
21 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0048 others(18): Show |
21 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.1182+5284_1182+529 others(14): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(4): Show |
6 | a0001c0001t0001g0049 a0001c0001t0001g0235 a0002c0002t0002g0100 others(3): Show |
6 | HG02886.hp2 NA18940.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1182+5283_1182+529 others(15): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(5): Show |
6 | a0001c0001t0001g0054 a0002c0002t0002g0051 a0002c0002t0002g0064 others(3): Show |
6 | HG00735.hp1 HG01069.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1182+5282_1182+529 others(16): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(6): Show |
5 | a0001c0001t0001g0027 a0002c0002t0002g0063 a0002c0002t0002g0226 others(2): Show |
5 | HG02027.hp1 NA18747.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182+5281_1182+529 others(17): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(7): Show |
5 | a0001c0001t0001g0163 a0002c0002t0002g0224 a0002c0002t0002g0229 others(2): Show |
5 | HG01167.hp1 HG01256.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182+5280_1182+529 others(18): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(8): Show |
4 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0002c0002t0002g0044 others(1): Show |
4 | HG02074.hp2 NA18973.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+5279_1182+529 others(19): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(9): Show |
4 | a0001c0001t0001g0159 a0001c0003t0001g0256 a0002c0002t0001g0150 others(1): Show |
4 | HG02071.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+5278_1182+529 others(20): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(10): Show |
3 | a0001c0001t0001g0158 a0001c0001t0001g0279 a0002c0002t0002g0240 |
3 | HG02165.hp2 HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1182+5277_1182+529 others(21): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(11): Show |
4 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0277 others(1): Show |
4 | HG03453.hp2 NA18971.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+5276_1182+529 others(22): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(12): Show |
4 | a0001c0001t0001g0097 a0001c0001t0001g0178 a0001c0001t0001g0308 others(1): Show |
4 | HG02040.hp1 HG03540.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+5275_1182+529 others(23): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(14): Show |
2 | a0001c0001t0001g0162 a0001c0001t0001g0164 |
2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1182+5273_1182+529 others(25): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(15): Show |
2 | a0001c0001t0001g0052 a0001c0001t0001g0278 |
2 | HG03041.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1182+5272_1182+529 others(26): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | G | GTTTTTTT others(17): Show |
1 | a0002c0002t0001g0149 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1182+5270_1182+529 others(28): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | GT | G | 7 | a0001c0001t0002g0187 a0001c0001t0003g0244 a0001c0001t0003g0245 others(4): Show |
7 | HG01256.hp1 HG01258.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1182+5293delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | GTTT | G | 16 | a0001c0001t0001g0142 a0001c0001t0001g0285 a0001c0001t0001g0298 others(13): Show |
16 | HG00597.hp1 HG00642.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1182+5291_1182+529 others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | GTTTT | G | 23 | a0001c0001t0001g0284 a0001c0001t0001g0287 a0001c0001t0001g0292 others(20): Show |
23 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1182+5290_1182+529 others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | GTTTTTT | G | 10 | a0001c0001t0001g0175 a0001c0001t0001g0262 a0001c0001t0001g0264 others(7): Show |
10 | HG00738.hp1 HG01243.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182+5288_1182+529 others(10): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | GTTTTTTT others(2): Show |
G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(20): Show |
26 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1182+5285_1182+529 others(13): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | GTTTTTTT others(4): Show |
G | 1 | a0002c0002t0002g0072 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1182+5283_1182+529 others(15): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | GTTTTTTT others(6): Show |
G | 1 | a0002c0002t0002g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1182+5281_1182+529 others(17): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | GTTTTTTT others(7): Show |
G | 4 | a0002c0002t0002g0028 a0002c0002t0002g0029 a0002c0002t0002g0060 others(1): Show |
4 | HG01496.hp1 HG02738.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+5280_1182+529 others(18): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | GTTTTTTT others(8): Show |
G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1182+5279_1182+529 others(19): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | GTTTTTTT others(9): Show |
G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG02886.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1182+5278_1182+529 others(20): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151731 | GTTTTTTT others(12): Show |
G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG02258.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+5275_1182+529 others(23): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151731 | ||||||
| chr2:58151739 | T | C | 2 | a0001c0003t0001g0009 a0001c0003t0001g0010 |
2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1182+5265T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151739 | |||||||
| chr2:58151740 | T | C | 5 | a0001c0003t0001g0012 a0001c0003t0001g0015 a0001c0003t0004g0011 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182+5266T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151740 | |||||||
| chr2:58151744 | T | TTTTTTTT others(13): Show |
1 | a0001c0001t0001g0031 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1182+5289_1182+529 others(24): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58151744 | ||||||
| chr2:58151746 | T | G | 1 | a0002c0002t0002g0066 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1182+5272T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151746 | |||||||
| chr2:58151769 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1182+5295G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151769 | |||||||
| chr2:58151807 | C | T | 108 | a0001c0001t0001g0274 a0001c0001t0001g0284 a0001c0001t0001g0285 others(105): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1182+5333C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151807 | |||||||
| chr2:58151883 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1182+5409A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151883 | |||||||
| chr2:58151939 | G | A | 1 | a0005c0006t0002g0166 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1182+5465G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58151939 | |||||||
| chr2:58152035 | A | C | 3 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0006c0010t0001g0148 |
3 | HG02886.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1182+5561A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58152035 | |||||||
| chr2:58152284 | G | A | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+5810G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58152284 | |||||||
| chr2:58152361 | A | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(252): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1182+5887A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58152361 | |||||||
| chr2:58152385 | T | A | 87 | a0001c0001t0002g0016 a0002c0002t0001g0253 a0002c0002t0002g0003 others(84): Show |
88 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1182+5911T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58152385 | |||||||
| chr2:58152694 | A | AT | 10 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0169 others(7): Show |
11 | HG00423.hp1 NA18955.hp1 NA18969.hp2 others(8): Show |
intron_variant | MODIFIER | c.1182+6229dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58152694 | ||||||
| chr2:58152876 | C | T | 1 | a0001c0001t0002g0018 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1182+6402C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58152876 | |||||||
| chr2:58153032 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(167): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1183-6317G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153032 | |||||||
| chr2:58153134 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1183-6215T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153134 | |||||||
| chr2:58153155 | A | G | 16 | a0001c0001t0001g0142 a0001c0003t0001g0009 a0001c0003t0001g0010 others(13): Show |
16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1183-6194A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153155 | |||||||
| chr2:58153166 | G | T | 20 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(17): Show |
20 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.1183-6183G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153166 | |||||||
| chr2:58153279 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01167.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1183-6070T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153279 | |||||||
| chr2:58153386 | C | G | 5 | a0001c0001t0001g0119 a0001c0001t0001g0277 a0001c0001t0001g0278 others(2): Show |
5 | HG02145.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1183-5963C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153386 | |||||||
| chr2:58153516 | G | A | 12 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(9): Show |
12 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1183-5833G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153516 | |||||||
| chr2:58153523 | G | C | 87 | a0001c0001t0002g0016 a0002c0002t0001g0253 a0002c0002t0002g0003 others(84): Show |
88 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1183-5826G>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153523 | |||||||
| chr2:58153586 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1183-5763C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153586 | |||||||
| chr2:58153613 | G | A | 2 | a0001c0001t0001g0123 a0007c0009t0001g0124 |
2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1183-5736G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153613 | |||||||
| chr2:58153693 | G | T | 9 | a0001c0001t0001g0142 a0001c0003t0001g0261 a0001c0003t0001g0263 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183-5656G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153693 | |||||||
| chr2:58153832 | G | T | 2 | a0001c0001t0001g0259 a0001c0001t0001g0327 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1183-5517G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58153832 | |||||||
| chr2:58154070 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1183-5279A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154070 | |||||||
| chr2:58154242 | A | T | 16 | a0001c0001t0001g0142 a0001c0003t0001g0009 a0001c0003t0001g0010 others(13): Show |
16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1183-5107A>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154242 | |||||||
| chr2:58154256 | A | AT | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1183-5087dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58154256 | ||||||
| chr2:58154277 | T | G | 11 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1183-5072T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154277 | |||||||
| chr2:58154321 | CT | C | 32 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(29): Show |
32 | HG01099.hp2 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.1183-5018delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58154321 | ||||||
| chr2:58154371 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1183-4978T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154371 | |||||||
| chr2:58154615 | G | A | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1183-4734G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154615 | |||||||
| chr2:58154650 | T | C | 72 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(69): Show |
76 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1183-4699T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154650 | |||||||
| chr2:58154704 | A | C | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1183-4645A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58154704 | |||||||
| chr2:58155011 | T | A | 2 | a0001c0001t0001g0297 a0001c0001t0001g0301 |
2 | NA18971.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1183-4338T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155011 | |||||||
| chr2:58155079 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1183-4270T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155079 | |||||||
| chr2:58155355 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0019 others(184): Show |
193 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.1183-3994G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155355 | |||||||
| chr2:58155488 | T | TGGGAAGT others(2): Show |
11 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1183-3861_1183-386 others(13): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155488 | |||||||
| chr2:58155556 | A | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(56): Show |
62 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.1183-3793A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155556 | |||||||
| chr2:58155579 | A | G | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1183-3770A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155579 | |||||||
| chr2:58155613 | C | T | 2 | a0001c0001t0001g0291 a0001c0001t0001g0302 |
2 | HG00438.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.1183-3736C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155613 | |||||||
| chr2:58155766 | A | C | 1 | a0002c0002t0002g0152 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1183-3583A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155766 | |||||||
| chr2:58155917 | G | GT | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(7): Show |
10 | HG01891.hp1 HG02109.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1183-3429dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58155917 | ||||||
| chr2:58155917 | G | GTT | 11 | a0001c0001t0001g0142 a0001c0001t0001g0249 a0001c0001t0001g0250 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1183-3430_1183-342 others(6): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58155917 | ||||||
| chr2:58155920 | TG | T | 15 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(12): Show |
15 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1183-3428delG | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155920 | |||||||
| chr2:58155921 | G | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(69): Show |
74 | HG00423.hp2 HG00735.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.1183-3428G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155921 | |||||||
| chr2:58155921 | GT | G | 77 | a0001c0001t0001g0262 a0001c0001t0001g0264 a0001c0001t0001g0300 others(74): Show |
81 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1183-3415delT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58155921 | ||||||
| chr2:58155925 | T | G | 14 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
14 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1183-3424T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155925 | |||||||
| chr2:58155946 | A | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0140 |
2 | HG02300.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1183-3403A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155946 | |||||||
| chr2:58155954 | G | A | 11 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0114 others(8): Show |
11 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1183-3395G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58155954 | |||||||
| chr2:58156140 | G | GC | 10 | a0001c0001t0001g0119 a0001c0001t0001g0160 a0001c0001t0001g0161 others(7): Show |
10 | HG01167.hp1 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1183-3205dupC | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156140 | ||||||
| chr2:58156141 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1183-3208C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156141 | |||||||
| chr2:58156160 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1183-3189A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156160 | |||||||
| chr2:58156171 | A | G | 2 | a0003c0005t0001g0116 a0003c0005t0001g0117 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1183-3178A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156171 | |||||||
| chr2:58156263 | T | C | 9 | a0001c0001t0001g0142 a0001c0003t0001g0261 a0001c0003t0001g0263 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183-3086T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156263 | |||||||
| chr2:58156366 | C | T | 1 | a0001c0001t0002g0200 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1183-2983C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156366 | |||||||
| chr2:58156579 | GTTTTT | G | 6 | a0001c0001t0001g0175 a0001c0001t0001g0179 a0001c0001t0001g0262 others(3): Show |
6 | HG00738.hp1 HG01243.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1183-2766_1183-276 others(9): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156579 | ||||||
| chr2:58156580 | T | G | 16 | a0001c0001t0001g0142 a0001c0003t0001g0009 a0001c0003t0001g0010 others(13): Show |
16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1183-2769T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156580 | |||||||
| chr2:58156583 | T | A | 1 | a0003c0005t0001g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1183-2766T>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156583 | |||||||
| chr2:58156583 | T | TTTTTGTT others(8): Show |
1 | a0001c0001t0002g0205 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1183-2746_1183-273 others(19): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156583 | ||||||
| chr2:58156583 | TTTTTG | T | 36 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0104 others(33): Show |
36 | HG00423.hp2 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1183-2736_1183-273 others(9): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156583 | ||||||
| chr2:58156585 | TTTG | T | 13 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0144 others(10): Show |
13 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1183-2761_1183-275 others(7): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156585 | ||||||
| chr2:58156588 | G | T | 16 | a0001c0001t0001g0142 a0001c0003t0001g0009 a0001c0003t0001g0010 others(13): Show |
16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1183-2761G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156588 | |||||||
| chr2:58156609 | TTTTG | T | 7 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1183-2736_1183-273 others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156609 | ||||||
| chr2:58156613 | G | GT | 9 | a0001c0001t0001g0142 a0001c0003t0001g0261 a0001c0003t0001g0263 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183-2731dupT | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58156613 | ||||||
| chr2:58156685 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(156): Show |
165 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.1183-2664C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58156685 | |||||||
| chr2:58157073 | A | G | 2 | a0001c0001t0003g0244 a0001c0001t0003g0245 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1183-2276A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58157073 | |||||||
| chr2:58157300 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0179 |
2 | HG00738.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1183-2049A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58157300 | |||||||
| chr2:58157647 | T | C | 1 | a0002c0002t0002g0329 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1183-1702T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58157647 | |||||||
| chr2:58157692 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
9 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183-1657A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58157692 | |||||||
| chr2:58157714 | C | T | 1 | a0002c0002t0002g0037 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1183-1635C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58157714 | |||||||
| chr2:58157947 | T | C | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0003c0005t0001g0116 others(1): Show |
4 | HG02109.hp2 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183-1402T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58157947 | |||||||
| chr2:58158092 | A | G | 24 | a0001c0001t0001g0259 a0001c0001t0001g0309 a0001c0001t0001g0310 others(21): Show |
24 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1183-1257A>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158092 | |||||||
| chr2:58158108 | T | G | 18 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0012 others(15): Show |
18 | HG01069.hp1 HG01256.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1183-1241T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158108 | |||||||
| chr2:58158150 | G | A | 2 | a0001c0003t0001g0009 a0001c0003t0001g0010 |
2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1183-1199G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158150 | |||||||
| chr2:58158170 | T | TCTTA | 93 | a0001c0001t0001g0142 a0001c0001t0001g0158 a0001c0001t0001g0159 others(90): Show |
97 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1183-1177_1183-117 others(8): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58158170 | ||||||
| chr2:58158182 | T | C | 3 | a0001c0003t0004g0011 a0001c0003t0004g0013 a0001c0003t0004g0014 |
3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1183-1167T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158182 | |||||||
| chr2:58158187 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1183-1162T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158187 | |||||||
| chr2:58158218 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1183-1131T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158218 | |||||||
| chr2:58158341 | A | C | 1 | a0001c0001t0001g0031 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1183-1008A>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158341 | |||||||
| chr2:58158375 | C | G | 2 | a0001c0003t0001g0257 a0001c0003t0001g0258 |
2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1183-974C>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158375 | |||||||
| chr2:58158544 | T | TAA | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0061 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1183-803_1183-802d others(4): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 58158544 | ||||||
| chr2:58158651 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1183-698C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158651 | |||||||
| chr2:58158717 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0327 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1183-632G>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158717 | |||||||
| chr2:58158780 | C | A | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(2): Show |
5 | HG02615.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1183-569C>A | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158780 | |||||||
| chr2:58158815 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1183-534C>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58158815 | |||||||
| chr2:58159112 | G | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0019 others(113): Show |
118 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(115): Show |
intron_variant | MODIFIER | c.1183-237G>T | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58159112 | |||||||
| chr2:58159183 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA19001.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1183-166T>C | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58159183 | |||||||
| chr2:58159201 | T | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1183-148T>G | VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 12/12 | chr2 | 58159201 |